Extracellular DNA Traps: Origin, Function and Implications for Anti-Cancer Therapies

Medina Mamtimin; Akif Pinarci; Chao Han; Attila Braun; Hans-Joachim Anders; Thomas Gudermann; Elmina Mammadova-Bach

doi:10.3389/fonc.2022.869706

. 2022 Apr 27;12:869706. doi: 10.3389/fonc.2022.869706

Extracellular DNA Traps: Origin, Function and Implications for Anti-Cancer Therapies

Medina Mamtimin ^1,², Akif Pinarci ¹, Chao Han ^1,², Attila Braun ¹, Hans-Joachim Anders ^1,², Thomas Gudermann ^1,³, Elmina Mammadova-Bach ^1,^2,^*

PMCID: PMC9092261 PMID: 35574410

Abstract

Extracellular DNA may serve as marker in liquid biopsies to determine individual diagnosis and prognosis in cancer patients. Cell death or active release from various cell types, including immune cells can result in the release of DNA into the extracellular milieu. Neutrophils are important components of the innate immune system, controlling pathogens through phagocytosis and/or the release of neutrophil extracellular traps (NETs). NETs also promote tumor progression and metastasis, by modulating angiogenesis, anti-tumor immunity, blood clotting and inflammation and providing a supportive niche for metastasizing cancer cells. Besides neutrophils, other immune cells such as eosinophils, dendritic cells, monocytes/macrophages, mast cells, basophils and lymphocytes can also form extracellular traps (ETs) during cancer progression, indicating possible multiple origins of extracellular DNA in cancer. In this review, we summarize the pathomechanisms of ET formation generated by different cell types, and analyze these processes in the context of cancer. We also critically discuss potential ET-inhibiting agents, which may open new therapeutic strategies for cancer prevention and treatment.

Keywords: extracellular DNA traps, cancer, inflammation, immunity, thrombosis, anti-cancer therapies

Introduction

Extracellular deoxyribonucleic acid (DNA) can be detected in extracellular environments, including serum, urine, spinal fluid, amniotic fluid, cerebrospinal fluid, lymph, bile and milk. In 1948, Mandel and Métais described for the first time the presence of DNA in the plasma of cancer patients (1). Extracellular DNA comprises nuclear or mitochondrial DNA associated with proteins or extracellular vesicles (2). Pioneer studies by Leon et al., described that patients with cancer have elevated levels of extracellular DNA, and its reduction following radiotherapy could significantly improve the clinical conditions (3). Follow-up studies provided evidence that extracellular DNA levels are elevated in many cancer patients, especially with invasive metastatic cancer (3–5). Liquid biopsy-based diagnostic and prognostic approaches including the analysis of circulating tumor cells, ribonucleic acids (RNAs), extracellular vesicles and extracellular DNA became powerful tools for the therapeutic management of cancer patients (6–8). However, the variability of tumor-specific markers in extracellular DNA sequences and alterations in levels of extracellular DNA in cancer patients raised several questions about their origin. Two different hypotheses explained the origin of extracellular DNA; extracellular DNA is the product of cellular breakdown or generated by an active release mechanism (9). Cellular breakdown induces DNA release from dividing cancer cells, or products of cell lysis, apoptosis or necrosis following cancer treatments (10, 11). The theory of active release mechanism was supported by studies describing neutrophil-extracellular traps (NETs) as a process of immune defense inducing extracellular DNA release together with histones, radical oxygen species (ROS), peroxidases to trap and eradicate pathogens (12). Clinical and experimental studies highlighted the pivotal role of neutrophils in inflammation, thrombosis and cancer (13). NETs were found in liquid and tissue biopsies of cancer patients (14–18). Over the last years, many studies linked the process of NETosis to oncogenic transformation, angiogenesis, cancer development and metastasis (19, 20). In different pathological contexts (thromboinflammation, atherosclerosis, systemic lupus erythematosus, infection, sepsis), it became also evident that other blood, immune and specialized cells could also generate extracellular traps (ETs) (21, 22). In this review, we provide a detailed analysis of extracellular DNA function in cancer and also discuss the different sources and origins of ETs and provide the hypotheses on their possible impact on tumor cells and tumor microenvironment.

Neutrophil Extracellular Traps

Under physiological conditions, polynuclear neutrophils represent the main subpopulation of white blood cells, approximately 50-70% of circulating leukocytes (23). Neutrophils are produced in the bone marrow and differentiate from hematopoietic stem cell precursors (24). Their number oscillates in the peripheral blood and is regulated by the circadian rhythm (25). Neutrophils play an important effector role in innate immunity, constantly patrolling the organism against microbial infections and invading pathogens (26). Neutrophils respond to pathogens in several ways: phagocytosis (27) and release of granular contents (28) and NETs (12). Neutrophils express many inflammatory mediators, such as complement components (29), receptors for Fc fragments of immunoglobulins, integrins and cytokines, thereby regulating host defense, inflammation and cell-cell interactions (30). Neutrophils have polylobulated nuclei composed of 3-5 lobules (31), and secretory granules in the cytoplasm (32). Neutrophil granules are classified into 4 categories, based on their granule content (33); primary or azurophilic granules, containing myeloperoxidase (MPO), anti-microbial peptides (defensins), β-glucuronidase (34), lysozyme and serine proteases (neutrophil elastase (NE), cathepsins G, proteinases 3 (PR3), inducible nitric oxide synthase (iNOS) (35), secondary or specific granules containing lactoferrin, matrix metalloproteinase (MMP) 8 (36), tertiary or gelatinase granules containing MMP9 (37), LL-37 (38), NADPH oxidase and mobilizable secretory vesicles containing various surface membrane receptors (39). The granular content of neutrophils plays an important role in NETosis (12). Consistently, immature neutrophils with reduced granular content from acute myeloid leukemia patients had a lower potential to induce NETosis after phorbol 12-myristat 13-acetate (PMA) stimuli (40).

In 2004, research groups of Zychlinsky and Brinkmann demonstrated that neutrophils in response to pathogens generate extracellular fibers composed of decondensed DNA, decorated with anti-microbial peptides and other proteins from different cell compartments, and later this process was defined as NETosis (12, 41). NETosis was induced by stimulation of neutrophils with pathogens (fungi, bacteria, protozoa, parasites), bacterial lipopolysaccharide (LPS), interleukin 8 (IL8) or chemical stimulation with protein kinase C (PKC) activator PMA, indicating that NETs are involved in inflammatory and infectious processes (12, 42, 43). Endothelial cell-derived cytokines, such as IL8 also act on neutrophils, thereby inducing NET formation (44). NETs have been found in the blood of septic patients (45–47). Platelet-derived Toll-like receptor 4 (TLR4) appeared to play an essential role in the NET formation through binding to the bacterial LPS (48).

Depending on the stimulation of ET release, neutrophils become apoptotic (lethal NETosis) or can still survive (vital NETosis). The process of lethal NETosis is often induced by pharmacological, autoimmune or metabolic compounds or bacterial peptides (49–51). In contrast, vital NETosis is preferentially induced by molecules associated with pathogen-associated molecular pattern molecules (PAMPs), which are recognized by TLRs of the innate immune system and also by bacterial peptides (48, 52–54).

NET webs and granular proteins can eradicate a wide range of pathogens by ensuring their capture, providing a scaffold for protein binding, degrading pathogen toxins and by providing a high local concentration of anti-microbial molecules (43).

Molecular Mechanisms of Neutrophil Extracellular Trap Formation

At the molecular level, NETosis is regulated by MEK (MAPK/ERK kinase) or ERK (Extracellular-signal Regulated Kinase) (55), IRAK (IL1 Receptor-Associated Kinase) (56), PKC (57), Phosphoinositide 3-kinase (PI3K) (58) and AKT (59) pathways, inducing ROS production in response to the inflammatory mediators (60, 61), PMA (62), microorganisms (63, 64) and immune complexes (62, 65, 66). Terminally differentiated neutrophils undergo NETosis followed by the reactivation of cyclin-dependent kinase 6 (CDK6). Consequently, inhibition or knock-out of CDK6 function leads to reduced ability of neutrophils to induce NETosis (67). Some of these pathways are highly dependent on the NADPH oxidase 2 (Nox2), and ROS production (59). Nox2 is a multidomain complex enzyme, and its activity is regulated by protein PKC-dependent activation of p47phox, p67phox and p21rac subunits which form complex with b558 (68, 69). ROS production in neutrophils generates an optimal pH (7.5-8.5) for NE and MPO which are essential for NETosis (70). Consistently, neutrophils isolated from MPO-deficient patients display impaired bacterial killing and NETosis upon stimulation with PMA (71). The increase in pH level stimulates ROS production and induces histone H4 cleavage (70). In PMA-stimulated neutrophils hypochlorous acid (HOCl) disassembles the azurosome, leading to the release of NE into the cytoplasm (72). Later, NE degrades F-actin and translocates into the nucleus and breaks histone H1 (73). NE and MPO facilitate chromatin decondensation and the loss of lobular structure of the nucleus. Following this process, the nuclear envelope disassembles into vesicles thereby mixing both the cytoplasm and nucleoplasm. In the cytoplasm, decondensed chromatin binds granular and cytoplasmic anti-microbial proteins such as NE and MPO, before rupturing the cytoplasmic membrane for NET formation (49, 74). Interestingly, NET formation upon stimulation with PMA or crystals (nano- and microparticles) can also involve receptor-interacting serine/threonine-protein kinases (RIPK1 and RIPK3) and mixed lineage kinase domain-like pseudokinase (MLKL)-dependent pathway of necroptosis (75–77).

NETs can also form independently of Nox-signaling. This occurs through an influx of extracellular calcium (Ca²⁺) through Ca²⁺ ionophores, such as ionomycin and A32178 which are secreted by the gram-positive bacteria (78–80). Although Nox-induced ROS production is not involved in this type of NETosis, Ca²⁺ ionophores can induce ROS production using an alternative pathway in the mitochondria (81). Nox-independent NETosis needs potassium (K⁺) influx through the activation of small-conductance Ca²⁺-activated K⁺ SK3 channels. In this pathway, ERK and Akt signaling are activated at low or moderate levels, compared to Nox-dependent NETosis, and similar levels of p38 activation were found in both pathways (82).

Tumor-Associated NETs

NET formation was detected in different phases of tumor progression and metastasis (14, 17, 83–85), ( Figure 1 ). At the early phase of cancer, NETosis supports the epithelial-mesenchymal transition. Treatment of gastric and breast cancer cells with NETs induces an aggressive mesenchymal phenotype, thereby increasing cancer progression (86, 87). NETs induce gene expression of cancer stem cell marker CD24, and proinflammatory factors, such as IL1β, IL6, IL8, CXC motif chemokine receptor 1 (CXCR1), MMP2, MMP9 in cocultured luminal breast cancer cells (86). NETs also promote epithelial-mesenchymal transition in pancreatic ductal adenocarcinoma (PDAC). In clinical settings, increased levels of NETs were correlated with epithelial-mesenchymal transition markers in patients diagnosed with PDAC (88). At a later phase, the primary tumor starts to express many factors to stimulate NETosis. Systemic inflammation and hypoxia in the tumor and tumor microenvironment are important factors to induce neutrophil infiltration and NETosis (89–91). Hypoxia increases the levels of β2 integrin on the neutrophil surface in a hypoxia-inducible factor-1α (HIF1α)-dependent manner, and consequently, pharmacological blockade or knock-down of HIF1α in neutrophils inhibits NET formation (92, 93). HIF-2α also contributes to the recruitment of neutrophils to colon tumors, enhancing colon cancer progression through enhancing CXCL1 chemokine expression (94). Several other chemokines and cytokines are involved in the regulation of cancer-associated NETosis, regulating diverse signaling pathways. In human and mouse breast cancer, recent studies reported the role of tumor cell-secreted protease cathepsin C-mediated signaling in neutrophil recruitment and NET formation. In this pathological context, cathepsin C activates neutrophil membrane-bound proteinase 3 (PR3), thereby facilitating IL1β and Nuclear Factor kappa-light-chain-enhancer of activated B cells (NF-kb) activation, which in turn enhances neutrophil recruitment through the upregulation of IL6 and C-C Motif Chemokine Ligand 3 (CCL3) (95). Cancer cells also release exosomes to stimulate neutrophil chemotaxis and NET formation. Colon cancer cells transfer mutant KRAS to the neutrophils through exosomes, thereby promoting NETosis through the upregulation of IL8 which subsequently induces tumor growth, invasion and migration (96). It has been shown that neutrophils isolated from peripheral blood of mice bearing chronic myeloid lymphoma, lung and breast carcinoma tumors are more prone to generate NETs compared to the neutrophils isolated from healthy mice (97). In cancer models, neutrophil depletion and or DNAse I injection restored vascular perfusion and prevented vascular leakage (98). NETs were also shown to enhance endogenous effector functions of thrombin in plasma, thereby inducing cancer cell migration, invasion and angiogenesis (16, 99–101).

Multiple roles of neutrophil extracellular traps (NETs) in tumor progression and metastasis. Neutrophils are mobilized from bone marrow, enter into the circulation and migrate towards proangiogenic and proinflammatory gradients. Neutrophils are recruited to the primary tumor site through various cytokines and chemokines such as CXCL1, IL6 or CCL3, ultimately leading to neutrophil activation and NET release. Cancer cell-derived exRNA can also induce NETs which in turn amplify the release of exRNA. In growing tumors, NETs enhance cancer progression by enhancing thrombin activity, increasing the expression of stem cell markers and inflammatory chemokines and cytokines and promoting epithelial-mesenchymal transition. NET formation is also enhanced by the uptake of exosomes transporting oncogenic mutations to the tumor sites. NETs regulate cancer cell migration and tumor growth by directly interacting with T cells, inducing the exhaustion of cytotoxic T cells and differentiation of naïve T cells into regulatory T cells, thereby promoting an immunosuppressive environment. During their transit in the circulatory system, cancer cells are captured by the chromatin web network of NETs and this physical and functional interaction provides shielding thereby protecting cancer cells from cytotoxic effects of immune cells. NETs also provide an “anchor” to the cancer cells, facilitating their adhesion and extravasation into the secondary tumor sites to form distant metastasis. CCDC25 is expressed by cancer cells and can serve as a NET-DNA receptor that senses NETs and recruits invasive cancer cells to the metastatic sites. During inflammation, NETs can activate dormant tumor cells and stimulate them to migrate and form metastasis by cleaving basement membrane components (laminins). NETs also induce thromboinflammation leading to ischemia and injury in organs, such as the heart and kidney. Cancer cell-derived G-CSF predisposes circulating neutrophils to form NETs through the recruitment of blood platelets. Interactions between platelets and neutrophils play an important role in cancer progression and metastasis by inducing platelet activation and NETosis and consequently enhancing tumor-associated coagulation and thrombosis.

NET formation was also detected in the metastatic niche and plays an important role in different steps of metastasis, including tumor cell adhesion (19, 102, 103), dissemination (14) and extravasation at the distant organs. Several proteases and adhesion molecules are present on NETs and facilitate tumor cell extravasation and metastasis (14, 104). It was proposed that NETs have a strong ability to trap circulating tumor cells, thereby protecting them from immune system-mediated destruction and promoting tumor cell dissemination and adhesion at distant organs (105, 106). The premetastatic niche formation in the omentum is supported by increased neutrophil mobilization and NET formation, creating a conducive environment for the seeding of ovarian cancer cells (20). In an orthotopic model of ovarian cancer, depletion of IL8, granulocyte colony-stimulating factor (G-CSF), CXCL chemokine growth regulated oncogenes (GROα/CXCL1 and GROβ/CXCL2) in primary tumor cells incompletely decreased NET formation and chemotaxis, thereby inhibiting subsequent omental metastasis (20). NETs were also shown to enhance cancer metastasis by activating tumor-intrinsic TLR4/9-cyclooxygenase 2 (COX2) inflammatory pathways (107). Altogether these results suggest that cytokines cooperate with many factors to optimally regulate neutrophil recruitment and NET formation, which in turn enhance the inflammatory landscape of tumor, thereby contributing to tumor metastasis.

The metastasized liver tissues isolated from breast or colon cancer contain a high number of NETs. If NETs are detected in the serum of cancer patients, this could be a predicting factor for the occurrence of liver metastases at very early stages. NETs can attract cancer cells from established distant metastases. This cellular motility was mediated by the cancer cell-resident transmembrane NET-DNA receptor coiled-coil domain containing 25 (CCDC25) which activates the integrin-linked kinase (ILK)-β-parvin pathway and thus senses extracellular DNA release (18).

NETs are also involved in dormant cell reactivation thereby increasing metastatic events in distant organs (108). During chronic pulmonary inflammation, NETs awake dormant breast cancer cells and promote metastasis. Degradation of thrombospondin 1 (TSP1) and remodeling laminin-based extracellular matrix are important steps to awake the dormant cells. Consistently, activation of laminin receptor integrin α3β1 and transcriptional regulator yes-associated protein (YAP) signaling is required for NET-dependent activation of dormant tumor cells. Furthermore, integrin β1 is involved in the activation of FAK-ERK-MLC2-YAP signaling pathway, which also contributes to tumor survival and growth (108).

Cancer cells can also induce NETosis through other alternative mechanisms. Lewis lung carcinoma (LLC) cancer cells release a high amount of RNAs, which accumulate in the extracellular space and activate epithelial cells, thereby inducing NETosis mediated by proinflammatory cytokines, such as IL1β. NETs reduce the lung epithelial barrier, induce necrosis and the release of extracellular RNAs (17).

NETs can directly interact with T cells and suppress the anti-tumor immunity through metabolic and functional exhaustion, emphasizing the deleterious effect of NETs during all the evolutionary stages of the tumor process, including tumor growth, angiogenesis and tumor metastasis. Blockade of NETosis in combination with programmed death-ligand 1 (PD-L1) immune checkpoint inhibitors enhance the response rates of colorectal cancer metastasis by improving the function of exhausted CD8+ cells (109). NETs also modulate regulatory gene profiles in naïve CD4+ T cells, promoting their differentiation into regulatory T cells (Tregs). This crosstalk between NETs and Tregs was shown to contribute to liver carcinogenesis in non-alcoholic steatohepatitis (110). NETs are also observed in bladder tumors of patients who did not respond to radiotherapy and persistent disease post-radiotherapy, wherein an elevated neutrophil-CD8+ ratio was associated with worse overall survival (111).

Cancer-Associated Thromboinflammation and NETosis

NETs provide a physical scaffold for thrombus formation by capturing platelets and red blood cells. Platelets are associated with NETs through binding of von-Willebrand Factor (vWF), fibronectin or immobilized fibrinogen (112). Interestingly, DNA was detected on the platelet surface of patients with systemic lupus erythematosus (113), indicating that platelets can directly bind DNA with histones in NETs, linking immune response to thrombosis. Growing tumors activate platelets by inducing uptake of tissue factor (TF)-derived extracellular vesicles (114, 115). Upon platelet activation, P-selectin is exposed to the surface which interacts with neutrophil-derived P-selectin glycoprotein ligand 1 (PSGL1), thereby promoting neutrophil-platelet interaction, subsequent neutrophil activation and NETosis (116). Thrombin-activated platelets primed neutrophils to NETosis in different in vitro and in vivo experimental conditions (116–118). Similar effects were observed when neutrophils were incubated with soluble P-selectin (116). In contrast, genetic or pharmacological blockade of P-selectin decreases NETosis (116). In clinical studies, increased P-selectin exposure on the activated platelet surface and increased soluble form of P-selectin are associated with venous thromboembolism (VTE) in cancer patients (119). Clark et al. showed that platelet-derived TLR4 induced platelet activation, platelet-neutrophil interaction and NETosis in the murine sepsis model (48). Platelet-derived high mobility group box 1 (HMGB1) can also activate neutrophil-resident TLR4 or binds to the receptor for advanced glycation end products (RAGE) on neutrophils, thereby inducing NETosis (118, 120). Furthermore, collagen and thrombin-activated platelets could also stimulate NETosis through HMGB1 (118). Thrombin-stimulated platelets also trigger MLKL-dependent necroptosis of neutrophils accompanied by NET release (121).

In the late stages of the breast carcinoma model, NETosis occurred concomitantly with the appearance of venous thrombi in the lung (97). Although this phenotype can be multifactorial, it is also closely linked to the role of neutrophils and platelets in the tumor microenvironment. Cancer predisposes neutrophils to generate NETs thus increasing platelet reactivity and hypercoagulability, thereby promoting primary tumor growth and stimulating tumor metastasis (97, 122, 123). NET formation is systematically correlated with the hypercoagulability state of cancer and thrombotic complications (16, 124, 125). During cancer progression, circulating DNA possibly induces the generation of thrombin, thereby activating the coagulation cascade (126). In an orthotopic mouse model of PDAC and human patients with PDAC, NET formation induces hypercoagulability by enhancing platelet aggregation responses through RAGE, DNA and TF release. Neutrophils isolated from RAGE-deficient mice had a lower ability to form NETs and circulating biomarkers of tumors and NETs were strongly reduced (127). Pancreatic cancer cells can stimulate NETosis through direct interactions with neutrophils or by priming platelets (128). Although blood clotting factors regulate neutrophil function (129), hypercoagulation was associated with the appearance of N2 protumoral neutrophils undergoing NETosis (130).

Apc^Min/+ (multiple intestinal neoplasia) mouse has a point mutation at the adenomatous polyposis coli (Apc) gene, and it is considered to be a model for human familial adenomatous polyposis (131). In this intestinal tumorigenesis model, hypercoagulation was associated with neutrophil recruitment and NETosis and these observed effects were dependent on the engagement of the complement 3a receptor (C3aR) (130). In other transgenic mouse tumor models (RIP1-Tag2 insulinoma and MMTV-PyMT breast cancer models), neutrophil recruitment and vascular leakage were observed in the kidney. Furthermore, platelet-neutrophil conjugates were accumulated in the kidney of tumor-bearing mice, which consequently generated NETs. The accumulation of NETs in the vasculature increased the levels of proinflammatory molecules, such as intercellular adhesion molecule 1 (ICAM1), vascular cell adhesion molecule 1 (VCAM1), E-selectin, IL1β, IL6 and CXCL1 (98).

Neutrophils of patients with myeloproliferative neoplasms characterized with a constitutively activating mutation of janus kinase 2 (JAK2) are also primed to generate NETs. Inhibition of constitutively active JAK2 could abolish NET formation and decreased thrombosis, suggesting an important role of platelet-associated NET formation in cancer-associated thrombosis (132). Tumor cells can synthesize G-CSF which stimulates the proliferation of circulating neutrophils, and consequently increases NET formation in the growing tumors (97, 133). High levels of G-CSF and NET-associated thrombi were found in patients with ischemic stroke and underlying cancer (134), indicating the link between systemic NET formation and arterial thrombosis. Heparin-induced thrombocytopenia (HIT) immune complexes induce NETosis via interaction with Fcγ receptor FcγRIIa on neutrophils and through neutrophil-platelet association (135). On another hand, neutrophil FcγRs can reprogram neutrophils into antigen cross-presenting cells thereby inducing acquired anti-tumor immunity (136).

Recent studies implicated neutrophils and NETs as central players in coagulation, organ injury and thromboinflammation that were detected in severe cases of severe acute respiratory syndrome coronavirus 2 (SARS-CoV2) infection (137). SARS-CoV2 was able to induce ROS and IL8 secretion and activate NETosis in human neutrophils (138). The angiotensin-converting enzyme (ACE2) and active transmembrane serine protease 2 (TMPRSS2) are also involved in this process (137).

Eosinophil Extracellular Traps

Eosinophil extracellular trap (EET) formation was detected in different human diseases ( Figure 2 ). EETs were observed in chronic obstructive pulmonary disease (COPD) sputum (139), and also in skin biopsies from patients with skin diseases such as Wells syndrome and bullous pemphigoids (140). In mouse models of atherosclerosis, eosinophils enhanced thrombus stability during arterial thrombosis (141). EET formation was detected in ruptured human atherosclerotic plaques and arterial thrombi (142). EETs were also observed in bronchial sections of a patient with allergic bronchopulmonary aspergillosis, which displayed eosinophil infiltrates in the mucus together with chromatolysis (143). Depending on the pathological conditions, EET formation is stimulated by different factors, released by pathogens, immune cells or cancer cells. In 2008, Yousefi et al., demonstrated that in vitro stimulation of eosinophils with LPS, C5a and or eotaxin/CCL11, by interferon gamma (IFNγ) and IL5-priming, induces the release EETs in a ROS-dependent manner. Interestingly, the majority of exposed EET DNAs are of mitochondrial origin (144). In vitro treatment of human eosinophils with thymic stromal lymphopoietin (TSLP) derived from epithelial cells induces the release of mitochondrial DNAs as well, and this process did not trigger cell death and was also dependent of Nox and β2 integrin functions (145). When eosinophils were primed with GM-CSF and activated with C5a, LPS or PMA, mitochondrial DNAs in EET were also observed, again excluding nuclear DNA and cell death in this process (146). However, EETs could be formed in the presence of cell death as well, involving extruded nuclear DNA and histones, indicating an alternative mechanism of EET formation (147). When eosinophils are exposed to Staphylococcus aureus, cells undergo nuclear disruption and cell death, leading to the release of nuclear DNAs and chromatin (145, 148). A similar process was observed when human eosinophils were stimulated with immunoglobulin IgG, IgA, a lipid mediator - platelet-activating factor (PAF), Ca²⁺ ionophore or PMA. In these experimental conditions, EETs were associated with histones and nuclear DNA. The release of nuclear EETs is mainly triggered by Nox-induced ROS production (147). However, depending on the experimental conditions, a ROS-independent mechanism was also observed when EET formation was induced by lysophosphatidylserine (LysoPS) through peptidyl arginine deiminase (PAD4)-mediated histone citrullination (149). Fungal species could also induce EET formation independently of ROS production, which occurred through CD11b binding and activation of Syk tyrosine kinase (143).

Eosinophils are specialized cells of the immune system, playing effector functions in allergic diseases, such as asthma (150). The percentage of EET-generating eosinophils was negatively correlated with lung function (151). Eosinophils express many receptors, adhesion molecules and integrins that allow their transit from the bone marrow to the blood (152–155). Eosinophil peroxidase activates and recruits dendritic cells to lymph nodes (156). The increased levels of eosinophil peroxidase and membrane-bound eosinophil granules in asthmatic patients lead to sputum rich in autoantibodies, such as anti-eosinophil peroxidase IgG, anti-nuclear, anti-double-stranded DNA and anti-histone antibodies (157). In allergic asthmatic diseases, peripheral blood eosinophils generate more EETs, when cells were challenged with LPS or IL5 in vitro (151). Challenging IL5 transgenic mice in a model of post-caecal ligation and intestinal puncture strongly enhanced eosinophil infiltration and EETs were observed in the intestinal tissues, protecting mice against sepsis (144). The authors found that in the colon and caecal tissues of mice and patients with Crohns disease, schistosomiasis and spirochetosis, extracellular DNA fibers were decorated with granular proteins such as major basic protein (MBP) and eosinophil cationic protein (ECP) (144). Besides these direct contacts, eosinophil MBP also enhances platelet activation inducing the release of bioactive molecules from α and δ granules or delivering activated TF, thereby contributing to the thrombus formation (141, 158, 159). Platelet-eosinophil interaction can induce EETs, triggered by IL5 release (141). EETs have also proinflammatory effects, subsequently activating epithelial cells to release proinflammatory cytokines such as IL6 and IL8 (151). In response to the opsonized Escherichia coli, activated eosinophils can release EETs, which had a strong bactericidal effect through a phagocytosis-independent mechanism (144).

Eosinophils and EETs were detected in the tumor tissues of patients with Hodgkin’s lymphoma (160). These patients had also increased expression of protease-activated receptor 2 (PAR-2) and nuclear p-ERK staining in cancer cells, which was detected together with abundant NETosis, fibrosis and TF-positive endothelium, pointing out the presence of tumor-associated inflammation and procoagulant phenotype (160). Eosinophils are also enriched in the circulating blood and tumor tissues in patients with other cancer types, such as colorectal, breast, ovarian, cervical, oral squamous and prostate cancer (161, 162). Eosinophils can transmigrate into the tumor microenvironment, following the interactions with endothelial cell-resident VCAM1 and ICAM1 (163). Cellular interactions of cancer cell-derived CCL24 and macrophage, fibroblast and eosinophil-derived CCL11 promote eosinophil recruitment to the tumor microenvironment (164–166). Cancer cell-derived chemokines (CCL3, CCL5) further support eosinophil migration (167, 168). Eosinophil-resident ST2, RAGE and TLR4 support migration towards the response to tumor necrotic cell alarmin mediators, IL33 and HMGB1 (163, 169–171). Furthermore, microbiota-released factors induce infiltration of eosinophils into the tumor microenvironment (172).

In summary, these results suggest that EETs play an important role in the activation and regulation of innate and adaptive immunity and are also involved in thromboinflammation. Based on EET DNA staining with eosinophil-specific markers, future studies are necessary to distinguish different sources of EETs. Precise, clinically relevant diagnostic tools will help to understand the phenotypic landscape of different cancers that are particularly enriched with eosinophils and propose more adequate therapeutic modalities.

Dendritic Cell Extracellular Traps

Dendritic cells can also form ETs ( Figure 3 ). It has been shown that a subset of dendritic cells, such as plasmacytoid dendritic cells, can recognize the hyphae of Aspergillus fumigatus through Dectin-2 and this interaction induces ET formation (DCETs) with anti-fungal activity and release of cytokines such as TNFα and IFNα. DCETs contain nuclear DNA with citrullinated histone H3, which shows similar structures as NETs (173). Interestingly, NETs can activate dendritic cells and trigger IFNγ production, driving autoimmune pathologies (173–175). In diabetes and cancer, dendritic cells also prime T cell immunity (175, 176). However, only limited information is available to dissect the role of DCETs in this pathology. Therefore, further studies are necessary on whether dendritic cells may influence cancer progression by forming DCETs and acting on T cell-mediated immunosuppression.

Molecular mechanisms of dendritic cell extracellular trap (DCET) formation and potential implications in cancer. A subset of dendritic cells, plasmacytoid dendritic cell-resident Dectin-2 interacts with the filamentous structure of pathogens (hyphae of *Aspergillus fumigatus*), thereby inducing ETs. These DCETs induce the release of cytokines such as TNFα and IFNα, eradicating pathogens. NETs may also activate dendritic cells, thereby triggering the production of IFNγ, which contributes to the pathogenesis of autoimmune diseases (diabetes). T cell priming by dendritic cells may contribute to the immunosuppression in the tumor microenvironment. The role of DCET in cancer remains elusive.

Monocyte and Macrophage Extracellular Traps

Monocytes and macrophages are critical components of the innate immune system, and play a key role in many pathological contexts, accumulating rapidly in the inflamed tissues (177). Monocyte and macrophage-extracellular traps (MoETs and METs) were visualized first time using scanning electron microscopy and immunofluorescence staining, detecting DNA fibers with specific dyes, such as DAPI, Hoechst, SYTOX, PicoGreen or TOPRO (49, 178, 179). ETs are generated from human peripheral blood monocytes (180, 181), human primary macrophages (182), human primary microglia and BV2 microglia (183), human placental macrophages (184), RAW 264.7 murine and U937 human monocyte-macrophage cells (50), THP-1 macrophage-like cells (184, 185), human glomerular macrophages (186), mouse J774A.1 macrophage-like cells (187), bovine (178, 179, 188) and caprine (189) monocytes. ETs in these cell types are composed of nuclear origin DNA fibers with MPO, citrullinated histone H3, elastase, MMP9, MMP12 and lysozyme (142, 180, 182, 187, 190). Besnoitia besnoiti is a cyst-forming apicomplexan protozoan parasite that causes bovine besnoitiosis which is traditionally endemic in Africa and Asia and also spreads in Europe. METs were detected when bovine or other mammalian species were exposed to pathogens tachyzoites of Besnoitia besnoiti (188). A highly pathogenic coccidian parasite Eimeria ninakohlyakimovae causes severe hemorrhagic typhlocolitis and in vitro exposure of caprine monocytes to sporozoites, sporocysts or oocysts could also induce MoETs (189). Non-infected monocytes derived from human peripheral blood can also form ETs.

Similar to the induction of NETosis, ET formation in monocytes can be triggered by PMA, A23187, PAF, or zymosan (180), ( Figure 4 ). MoETs contained MPO, lactoferrin, citrullinated histone H3, and elastase. The mitochondrial and nuclear origin of DNAs was confirmed with PCR and immunofluorescence staining of ETs. Although blockade of Nox activity in monocytes could inhibit MoETosis, this process was not affected upon treatment with MPO inhibitor 4-aminobenzoic acid hydrazide (ABAH), indicating that MoETosis is ROS-dependent, but MPO-independent in this experimental condition (180). In another study, exposure of macrophages to the yeast and bacteria-induced MET formation in J774A.1 mouse macrophages or primary mouse peritoneal macrophages, such an effect was not observed upon treatment with PMA, H₂O₂ and IFNγ, indicating an alternative way of ROS-independent METosis (187), ( Figure 5 ). However, others contrarily showed that the proinflammatory substances stimulate ROS, which subsequently induces the formation of METs (178, 182). Heme is one of the strong inducers of ROS production in immune cells (191). Elevated heme production and METs were frequently detected in patients with liver and kidney ischemic injury. In mice challenged with rhabdomyolysis-induced kidney injury, heme-activated platelets could induce METosis by increasing ROS production and histone citrullination (185). A follow-up study showed that hemin interacts with platelet-resident C-type lectin-like receptor 2 (CLEC-2) and Glycoprotein VI (GPVI), thereby inducing platelet activation and consequent MET formation (192, 193). Hemin interaction with platelets could enhance the enzymatic activity of Syk kinase and phospholipase Cγ (PLCγ). This concept was proved by using knockout mice with CLEC-2 or FcRγ deficiency in which attenuated renal dysfunction, tubular injury, and reduced METosis were observed, highlighting an important role of platelet (hem)ITAM-signaling in METosis (193). In atherothrombotic plaques isolated from patients with coronary thrombosis, both METs and NETs were detected. METs were more robust in intact lipid plaques and associated thrombi. Although NETs were also detected at the early step of thrombosis, METs were observed at the advanced stage in the organized thrombi (142). METs can generate thrombin and increase procoagulant activity, implying an important thrombogenic function (180).

Pathophysiological functions of monocyte extracellular traps (MoETs). During inflammation, ETs can be induced in activated monocytes, which occurs in Nox-dependent manner. Monocyte can release DNA from the nucleus and mitochondria, containing similar ET components such as histone 3, MPO, lactoferrin and elastase. During infectious and inflammatory processes, MoETs entrap pathogens, stimulate phagocytosis and also accelerate the thrombin generation, thereby enhancing procoagulant phenotype. During male genital tract infections and inflammation, spermatozoa induce ET formation in monocytes, which in turn inhibit their motility and reproductive system function. Crystal-induced MoETs have been suggested to contribute to a dysfunction of the intestinal barrier and intestinal epithelial cell necrosis ultimately leading to systemic inflammation.

Pathophysiological functions of macrophage extracellular traps (METs). Macrophages emit ETs following exposure to the pathogens (yeast, bacteria) and inflammatory mediators (glucose oxidase, dopamine, i.e. IFNγ, IL8, TNFα and HOCl). During organ injury, heme-activated platelets induce METosis by increasing the levels of ROS and histone citrullination. Heme binds to platelet receptors CLEC-2 and GPVI, and activates the (hem)ITAM-signaling pathways, triggered by Syk kinase and PLCγ activation, which ultimately promote METosis. METs are composed of mitochondrial or nuclear DNA and different proteins, amongst them are citrullinated histone 3, MPO, elastase, MMP-9, MMP-12 and lysozyme. Although METs display various bactericidal proteins, exposure to bacterial pathogens such as *Mycobacterium massiliense* triggers MET release and capture of bacteria, METs can also enhance bacterial growth. METs are also involved in the progression of coronary atherosclerosis and thrombosis as they are abundant components of late or organized thrombi and may contribute to the thrombus growth along with ETs released from other immune cells. Proinflammatory cytokines derived from adipocytes may also induce MET formation, indicating the potential implication of METs in obesity. METs are also found in solid tumors, such as pancreatic neuroendocrine and colon cancer. Tumor cell-derived growth factors and cytokines prime and activate macrophages to release ETs. In their turn, METs interact with cancer cells, further increasing their motile, migratory and invasive potential.

Adipose tissues isolated from obese patients contain a high number of macrophages which are infiltrating around dead adipocytes and forming a macrophage trap-like structure (194, 195). This tissue structure is frequently associated with increased levels of inflammatory cytokines, such as tumor necrosis factor α (TNFα), IL1β, and COX2 (196, 197). Exposure of RAW 264.7 macrophages to TNFα increased the levels of PAD2 and extracellular chromatin scaffold formation, indicating that inflammatory mediators released from adipocytes may stimulate METosis in the mammary fat pad environment. Interestingly, NET-specific PAD4 was absent in METs in the mammary fat pad (198). Macrophage activation is often correlated with a bad prognosis in many cancer types, including breast cancer, implying inflammation, accelerated tumor progression and metastasis (199). Furthermore, adipose tissue inflammation and obesity are also associated with an increased risk of breast cancer recurrence. MET formation may possibly correlate with these pathological signs and the severity of breast cancer. Recently Xu et al., identified several sources of NETs and METs in tumor tissues isolated from patients with pancreatic neuroendocrine cancer (200). The patients with high levels of NETs and METs have a postoperative cancer recurrence (200), indicating that these ETs may generate anti-cancer resistance mechanisms, leading to the cancer relapse.

Recent studies demonstrated METs could enhance in vitro invasion of HCT16 and SW480 colon cancer cells (201). Interestingly, exposure of macrophages to the conditioned cancer cell culture medium induced MET formation in a PAD2-dependent manner, indicating a positive feedback mechanism between MET and colon cancer cells. After PAD2 inhibitor treatment, the reduced MET formation was observed and consequently, the number of liver metastases was also decreased in mice, highlighting the contribution of METs to the tumor metastasis (201). In line with this, increased levels of tumor-associated METs were observed in human colon cancer tissues, predicting the poorest prognosis for colon cancer patients (201). Further studies are required to investigate how METs may induce motility, migration and invasion of colon cancer cells thereby leading to tumor metastasis.

Besides several experimental pieces of evidence showed that METosis has similar features as NETosis (49, 180, 182, 202, 203). Pathogens (bacteria, protozoa, fungi) and also spermatozoa, induce both MoET and NET formations, triggered by IL8-mediated activation of monocyte or neutrophils, respectively (12, 187, 202–204). In line with this, exposure of intestinal cells to the crystals of sevelamer, polystyrene sulfonate or cholestyramine could induce dysfunction of the epithelial cell barrier, associated with MoETosis and NETosis (205). Imbalanced gut microbiota and disrupted epithelial barrier represent an early subclinical phase of colitis-associated cancer (206). It could be interesting to evaluate whether the presence of MoETs or METs in these pathological conditions may represent a prognostic and diagnostic marker, thereby helping an earlier intervention.

Mast Cell Extracellular Traps

Mast cells have limited phagocytic activity compared to other immune cell types, therefore, the anti-microbial and anti-bacterial activity of these cells is mainly ensured by degranulation and release of anti-microbial peptides, such as defensins, proteases and cathelicidins (207, 208). Following exposure to pathogens, mast cells degranulate and release mast cell-extracellular traps (MCETs) in a ROS-dependent manner (209). MCETs are composed of classical components of ETs, such as DNA and histones and had inhibitory effects on bacterial growth. In contrast to other ETs, MCETs contain unique components such as mast-cell granule proteins tryptase and cathelicidin-related anti-microbial peptide (CRAMP/LL-37), ( Figure 6 ). Therefore, effective MCET degradation was possible using the mixture of DNAse I and tryptase-degrading enzymes (209). Interestingly, HIF1α can induce MCET formation thereby enhancing the anti-microbial activity of mast cells (210). During tumor growth, mast cells infiltrate into the growing tumors and remodel the tumor microenvironment by regulating immune and inflammatory reactions. In the melanoma cancer model, HIF1α together with histamine induces mast cell migration by increasing vascular endothelial growth factor (VEGF) production and consequent tumor angiogenesis (211). Tumor-infiltrating mast cells also potentiate tumor cell invasion and metastasis by interacting with cells in the tumor stroma (212–214). However, it is an open question whether mast cells can generate MCETs in response to the tumor microenvironment and how this process may influence cancer progression and metastasis.

Molecular mechanisms of mast cell extracellular trap (MCET) formation and potential implication in cancer. Another type of myeloid cells, mast cells also form ETs (MCETs). This response can be induced by the pathogens (bacteria, fungi), PMA, H₂O₂, cytokines and chemokines and occurs in a ROS-dependent manner. Although MCETs contain DNA and histones (orange), these ETs also entail granule derived tryptase (green) and anti-microbial peptide CRAMP/LL-37 (grey). Potentially, MCETs could play a role in cancer, as mast cells infiltrate the tumor microenvironment and promote invasion and metastasis of tumors. Furthermore, enhanced histamine levels activate and increase mast cell HIF1α and VEGF activity, contributing to tumor angiogenesis. HIF1α has been reported to enhance MCET formation in response to appropriate stimuli. In line with this assumption, hypoxic conditions in the tumor microenvironment could increase HIF1α levels in mast cells, thereby contributing to the mast cell activation and MCET formation and possibly contributing to the tumor progression and metastasis.

Basophil Extracellular Traps

Basophils are associated with inflammation, infection, immune defense and allergic response. Human basophils synthesize several proinflammatory and proangiogenic factors such as VEGF, angiopoietin and cysteinyl leukotriene C (215). Basophils also release histamine and produce IL4 and IL13 when cocultured with A549 lung carcinoma cells (216). Basophils produce ROS and form ETs upon IL3 priming and activation of complement factor 5a receptor or FcγRI (217). Although basophil extracellular traps (BaETs) contain mitochondrial DNA but not nuclear DNA, ET formation in basophils occurs in a Nox-independent manner (218), ( Figure 7 ). Basophils are present in the tumor microenvironment of human pancreatic and lung cancers and can induce inflammation-related skin tumor growth (219). Lung-resident basophils contribute to pulmonary development and promote M2 polarization of local macrophages (220). Besides their protumor functions, basophils located in melanoma cancer elicit anti-tumor properties by promoting tumor rejection via chemotaxis and infiltration of CD8+ T cells (221). Although these studies linked basophils to cancer development, the molecular mechanisms of BaET formation in cancer tissues and the consequent impact on tumor cell function have not been elucidated.

T Cell Extracellular Traps

Th17 cells belong to the CD4+ T-cell subset characterized by the production of IL17 and are considered an important mediator of inflammation, tissue homeostasis and cancer development (222, 223). Depending on their sensitivity to the microenvironmental stimuli, including cytokines and transcription factors, Th17 cells either enhance tumor growth and metastasis or promote anti-tumor immunity (224, 225). Like neutrophils, Th17 cells also play an important role in host defense against bacteria and pathogens (226). Recently, T cell extracellular trap (TCET) formation was observed, which was induced in this subset of activated T cells, releasing histone-rich TCETs in conjunction with anti-microbial proteins, thus trapping and killing bacteria (227), ( Figure 8 ). When peripheral blood T cells were isolated from healthy individuals and stimulated with the serum of patients with systemic lupus erythematosus, ET formation was observed (228), as well as after stimulation with anti-CD3/ anti-CD28 of CD8+ cells (229). Future studies are important to evaluate whether T cells can also form TCETs in response to tumor cells and tumor microenvironment and how TCETs may influence tumor growth, progression and tumor immunity.

B Cell Extracellular Traps

Only very limited results showed that B cells can also release extracellular traps (BCETs), ( Figure 8 ). Similar to TCETs, B cells were stimulated with the serum from patients with systemic lupus erythematosus and BCET formation was detected (228). It was hypothesized that BCETs could be a constant source of self-antigens for autoreactive B cells stimulating the production of antibodies (230).

Other Sources of Extracellular DNA

Endothelial Cell-Derived Extracellular DNA

DNA structures extruded from endothelial cells were observed during arterio-arterial embolization, a pathological condition occurring following cholesterol crystal-induced embolism in the kidney (231). Cholesterol crystal embolism is mobilized from an atherosclerotic plaque, followed by vessel obstruction, ischemia and organ failure (232). Studies by Shi et al., showed that injection of cholesterol crystals into the artery of the mouse kidney generates a thromboinflammatory environment with the presence of intravascular thrombi, composed of platelets, fibrin, neutrophils and extracellular DNA (231). Using in vitro cell culture experiments, exposure of neutrophils to cholesterol crystals or the supernatant of cholesterol crystal-activated platelets induced neutrophil necrosis and the release of chromatin and DNA to the cell culture supernatant (231). Interestingly, exposure to increasing doses of cholesterol crystals also induced necrosis of glomerular endothelial cells and consequent DNA release (231).

The vasculature of metastatic organs is frequently damaged and metastases can induce cell death (233). Necroptic cell death and subsequent DNA release occur in endothelial cells, involving RIPK1, RIPK3 and MLKL cell death signaling pathways. Tumor cell-induced endothelial necroptosis was shown as an important mediator of tumor cell extravasation and subsequent tumor metastasis (234). Further experiments need to be performed whether under certain conditions endothelial cells may also undergo ETosis.

Platelet-Derived Extracellular DNA

Platelets lack nuclear DNA and the amount of mitochondrial DNA is very limited, due to the few numbers of mitochondria per platelet (235). Theoretically, accumulated platelets at the injury sites may release mitochondrial DNA upon platelet activation (236, 237). This extracellular DNA may be contributed to immune cell-derived ETs, and further amplify cancer-associated thrombosis, thromboinflammation and tumor progression. Further studies are important to establish the role of platelet-derived ETs in these processes.

Cardiomyocyte-Derived Extracellular DNA

Cancer is associated with cachexia, vascular and metabolic dysregulation of the heart (238, 239). Cardiomyocytes possibly are a major source of extracellular DNA in patients with myocardial infarction (240, 241). Microvesicles and exosomes released from cardiomyocytes also contain extracellular DNA (242). Due to the limited experimental evidence, further studies are necessary to investigate the role of cardiomyocyte-derived extracellular DNA, analyze metabolic and DNA contents in patients with cancer and establish the contribution of ETs in myocardial infarction and cancer-associated heart dysfunction.

Tumor Cell-Derived Extracellular DNA and Horizontal Transfer of DNA

The blood plasma levels of extracellular DNAs are increased in human patients with breast, melanoma, pancreatic and colon cancers, which are directly extruded by cancer cells (4, 10, 243). Circulating extracellular DNA can interact with several molecules, exposed on the surface of blood cells, leading to the penetration of DNA (244, 245). Histones and complement factors directly bind and capture DNA (246–248). DNA can also be transferred to the exosomes and microparticles and secreted to the circulation. Indeed, circulating microvesicles isolated from the blood cancer patients contain fragments of mutated genes, such as phosphatase and tensin homolog (PTEN), p53 and KRAS (249–251). Cai and colleagues found that BCR/ABL hybrid genes can be transferred from chronic myeloid leukemia cells to the HEK293 and neutrophils, increasing DNA coding mRNA and protein levels (252). Similar results were observed with vascular smooth muscle cells and leukocyte-derived extracellular vesicles delivering the angiotensin receptor type 1 (AT1R) gene DNA to HEK293 cells and sex-determining region Y (SRY) DNA into the endothelial cells (253, 254).

Endogenous DNAse

DNAse enzymes are divided into two major families, DNAse I and DNAse II. Although DNAse I is found in exocrine gland secretions and blood, DNAse II derives from lysosomes/phagolysosomes (255). Regarding the sources of circulating DNA, it was assumed that tumor cells in cancer patients shed and release DNA into the bloodstream and this correlated with the pathogenesis of the disease (5, 256). In line with this, DNAse I levels in cancer patients are elevated during remission, and after successful interventions and decreased during cancer progression and metastasis. Furthermore, failure of DNAse levels to increase in response to treatment was correlated with poor prognosis (257, 258). However, DNAse activity in the blood was found to differ between healthy subjects and cancer patients and also varies between cancer types and stages of cancer (257–261). Indeed, decreased DNAse activity was found in patients with malignant lymphoma, gastrointestinal and prostate cancer (260, 262, 263), while the levels of DNAse activity were higher in breast cancer patients compared to the control (264). The physiological relevance of DNAse function in NETosis was proved in knockout mouse models. Mice with DNAse I and DNAse I like-3 enzyme deficiencies developed NETosis with intravascular clots and obstructed blood vessels which resulted in tissue damages of vital organs, such as the lung, liver and kidney (265). In humans, genetic mutations of DNAse are associated with autoimmune diseases such as systemic lupus erythematosus (266). DNAse X/Apo10 antibodies were found in patients with oral squamous cell carcinoma, indicating gene inactivation of DNA X in this type of tumor (267). A therapeutic strategy based on the delivery of transgenic vectors expressing DNAses was proposed to target DNA destruction or apoptosis. In 2011, Karli Rosner suggested an anti-cancer therapeutic approach based on human recombinant DNAse I. According to his approach, the replacement of apoptosis-activated endogenous DNAses with human recombinant DNAse I might help to bypass cancer defense mechanisms, increasing the killing efficiency of chemo and radiotherapy-resistant tumor cells (268). Since the inactivation of endogenous DNAse X gene was found in many tumor cells types, the strategies to restore the levels of DNAse X in cancer cells could be an important targeted therapy (267, 269). Delivery of vectors encoding several DNAses under one common promoter into the cancer cells could successfully induce apoptosis (268, 269).

Based on these findings, gene therapy was developed in a mouse model of colorectal cancer in which an adeno-associated virus (AAV) vector was used to express DNAse I in the liver, thereby suppressing the development of hepatic metastases. After AAV-DNAse I treatment, NETosis was inhibited in the tumor tissues with restored local immune responses by increasing the percentage of CD8+ T cells (270).

Exogenous DNAse I

Recombinant DNAse I has been successfully used as an anti-cancer agent and studied as a prognostic/diagnostic marker during cancer therapy. In 1961, de Lamirande determined the effect of DNAse and RNAse in mice bearing Ehrlich ascites carcinoma for the first time (271). After tumor cell implantation, daily injection of DNAse I could increase the survival rate of treated mice, but RNAse treatment did not affect mouse survival. A hypothesis was proposed, which included the uptake of DNAse into cancer cells, followed by necrosis and digestion of nuclear DNA (271). In other studies, the daily injection of RNAse and DNAse alone or in combination could enhance nuclease activity of blood plasma of tumor-bearing mice, and decrease the levels of extracellular DNA, back to the levels of control animals. Degradation of DNAs in the blood plasma was associated with reduced metastasis of LLC and hepatoma A–1 (HA-1) cancer cells (272–274). In the model of LLC, exogenous DNAse treatment not only inhibited metastasis but also increased DNAse activity in the blood, destroying extracellular DNA in the circulation of tumor-bearing mice by targeting tumor-associated DNA fragments such as short and long interspersed retrotransposable elements (SINEs and LINEs) and also oncogenic sequences (274, 275). Furthermore, daily intramuscular injection of bovine pancreatic DNAse I in LLC tumor model could also strongly decrease metastasis (276). In mouse models of melanoma, lymphosarcoma or pancreatic cancer, DNAse I treatment had also strong anti-tumor and anti-metastatic effects by destroying extracellular DNA (275, 277, 278). Bovine pancreatic DNAse also displayed anti-metastatic effects inhibiting the number of lymph nodes and lung metastasis in mouse models of leukemia and lymphoma cancers. Although bovine pancreatic DNAse I could inhibit the proliferation of several cancer cell types (Calu-1, SK-MES-1, HeLa, HEp-2 and L-929), it did not affect the peripheral blood mononuclear cells and fibroblasts (279). Combined treatment of DNAse I with proteases such as papain, trypsin or chymotrypsin led to a significant decrease of DNA content in the blood serum of rats, and no anti-tumor effects were observed in mice treated with proteases alone (280).

Pancreatic cancers belong to the group of diseases which affect both the endocrine and exocrine functions of the pancreas (281). The tumor microenvironment is instrumental in pancreatic tumor growth and metastasis. Although some mechanisms reflect tumor cell-autonomous processes, most require the interaction of tumor cells with tumor microenvironment, including endothelial cells, fibroblasts, and immune cells (282). In addition, chronic inflammation, thromboembolism and hypercoagulability are known as key features of PDAC (283, 284). Interestingly, DNAse I treatment of pancreatic cancer cells could strongly decrease tumor cell adhesion and migration, although tumor cell proliferation was not affected. In the orthotopic pancreatic cancer model, DNAse I treatment also strongly inhibited tumor burden and tumor metastasis to the liver and diaphragm, confirming the important pathological role of extracellular DNA in pancreatic cancer. Elevated CXCL8 secretion was detected in the medium of pancreatic cancer cell lines derived from liver metastases, in comparison with immortalized pancreatic ductal epithelial cells. Furthermore, the treatment of pancreatic cancer cells with recombinant CXCL8 could strongly increase extracellular DNA production (285). CXCL8 also induces ET formation in neutrophils, thereby enhancing cancer malignancy (14, 44, 96). DNAse I treatment strongly reduces ETs, and also the percentage of polymorphonuclear neutrophils that released observable ETs (286). Pancreatic tumor-bearing mice had also increased levels of NETs, and more rapid thrombotic occlusion in the injury model of jugular vein. DNAse I did not affect thrombotic occlusion in control mice, but protected tumor-bearing mice from enhanced venous thrombosis (287). These results suggest that enhanced NETosis contributes to thrombosis in pancreatic cancer.

Interestingly, DNAse I can also inhibit thrombosis independently of neutrophils. In the mouse model of cholesterol crystal embolism, in vivo depletion of circulating neutrophils in the peripheral blood did not influence the severity of disease, but DNAse I treatment significantly inhibited the numbers of obstructed vessels, decreased ischemic organ failure and kidney infarction. Preincubation of washed platelets with DNAse I inhibited platelet activation, P-selectin exposure, aggregation response to collagen, collagen-related peptide or thrombin. In addition, DNAse I-treated platelets formed less fibrin. DNAse I treatment also reduces the levels of secreted adenosine triphosphate (ATP) in human and mouse platelets, which strongly inhibits platelet aggregation, and ATP-dependent neutrophil activation (231, 288). Earlier, it was proposed that neutrophils are required for thrombosis in the laser-induced arterial injury model (289). Although DNAse I treatment induced the hydrolysis of ATP and adenosine diphosphate (ADP), decreasing fibrin formation and inhibiting thrombosis, scanning electron microscopy did not reveal classical NET structure in this thrombosis model (288).

Polyphosphate (polyP) is synthesized enzymatically from ATP and this metabolic conversion is fully reversible. PolyP is stored in dense granules of platelets, and secreted upon platelet activation. Extracellular polyP accelerates the coagulation cascade by factor V activation, promotes factor XI activation through thrombin and blocks the anti-coagulant activity of tissue factor inhibitor (TFI), thereby enhancing blood clotting (290). Interestingly, DNAse I could decrease ATP and polyP levels in vitro (231, 288, 291), indicating that DNAse I may inhibit ATP metabolism, or enhance ATP degradation or conversion of ATP to adenosine monophosphate (AMP). Altogether, these results suggest that the anti-thrombotic effects of DNAse I treatment in platelets may occur in an ATP/polyP-dependent manner.

Several experimental studies using cancer and thrombosis mouse models suggested that targeting extracellular DNA with DNAse I may offer a potential anti-cancer and anti-thrombotic strategy (278, 280, 292). However, only limited clinical studies with DNAse I treatment have been reported so far. In patients with cystic fibrosis, nebulized recombinant human DNAse treatment could reduce sputum viscosity and improve pulmonary function (293, 294). Therefore, recombinant human DNAse treatment is recommended in patients with cystic fibrosis and also in patients with other moderate or severe suppurative lung diseases. Further investigation is necessary whether DNAse I treatment may be effective in cancer or cancer-associated thromboinflammation.

Other Pharmacological Approaches

Aspirin

Aberrant arachidonic acid metabolism is involved in the inflammatory and carcinogenic processes (295). Aspirin (acetylsalicylic acid) irreversibly acetylates and thus inhibits the enzymatic activity COXs, thereby blocking the conversion of arachidonic acid to thromboxane A2 (TxA2) (296). In mouse models, aspirin treatment prevents NET-induced injury of the lung endothelium by inhibiting platelet activation and NETosis (297). A higher bacteria count in the blood was detected in aspirin-treated mice after infection, indicating that aspirin may interfere with NET functionality. However, this action of aspirin may be independent of platelet-resident COX activity, since aspirin-treated neutrophils had impaired NETosis (297, 298).

Prostaglandin E2

Prostaglandin E2 (PGE2) is a prostanoid fatty acid metabolic product of arachidonic acid. PGE2 inhibits PMA-induced NETosis through prostanoid receptors of EP2 and EP4 (299). Studies by Domingo-Gonzalez et al., showed that murine bone marrow transplant neutrophils which overexpress COX2 induce defective bacteria clearance (300). When these neutrophils were stimulated with PMA or rapamycin, NETosis was strongly reduced compared to control. After bone marrow transfer, NET formation was rescued using COX inhibitors. The same effect was achieved via EP2 receptor antagonist (PF-04418948) or EP4 antagonist (AE3-208) in neutrophils from bone marrow transplant mice and hematopoietic stem cell transplant patients (300).

In mice and healthy donors, NETosis was also inhibited by exogenously injected PGE2 which was dependent on the cAMP-PKA pathway (299, 300). Consistently, incubation of neutrophils with cAMP analog dibutyryl-cAMP, rolipram or butaprost could also inhibit NETosis (299).

Chloroquine

Chloroquine and hydroxychloroquine are anti-malarial drugs, which appeared as promising treatments also for cancer (301). Chloroquine inhibits autophagy in different cell types including neutrophils (127). Several groups have shown that autophagy promotes NETosis (62, 118, 302–304). However, studies using pharmacological inhibitors of autophagosome acidification and neutrophil- and eosinophil-autophagy‐related 5 (ATG5) conditional knock-out mice could not confirm these results (146). Chloroquine treatment reduces the severity of acute pancreatitis in mice, thereby improving survival (305). In cell culture assays, chloroquine could not diminish NETosis, indicating an indirect mechanism (306). Hydroxychloroquine is also known as an anti-inflammatory drug, which can block TLR/COX2 pathway-dependent NET formation and consequent metastasis in hepatocellular carcinoma (2, 107, 307). In the mouse model of PDAC, chloroquine treatment reversed hypercoagulability by reducing NET-mediated platelet aggregation and the release of circulating TF. Patients treated with hydroxychloroquine on a randomized protocol of preoperative chemotherapy showed a reduction in pre-operative VTE rate (127). Although several clinical trials showed the benefits of chloroquine as an anti-tumor drug (308), the precise molecular mechanisms of chloroquine-mediated effects has not been established. It was proposed that chloroquine may influence autophagy (309). Chloroquine in combination with other chemotherapeutic drugs could increase the efficiency of drug treatment, although it can accelerate chemotherapy-associated organ injury (301). Therefore, it is important to further investigate the effects of chloroquine on cancer-induced NETosis, thromboinflammation and organ injury.

Staphylokinase

Bacterial infection of host tissues activates neutrophils and induces NET formation, thereby activating the innate immune system, including macrophage phagocytosis. Interestingly, Staphylococcus aureus can escape from NETs, thus converting NETs to deoxyadenosine, thereby inducing immune cell death by caspase-3-mediated mechanism. Staphylococcus aureus can secret nuclease and adenosine synthase which modifies the structure of NETs, thereby destroying the NET-mediated immune defense system (310). Staphylococcus aureus also produces a plasminogen activator staphylokinase, which is a fibrin-specific thrombolytic biomolecule (311). Staphylokinase was proposed for the therapy of stroke and myocardial infarction. However, it has a short life-time in the blood, which limits the clinical application. Strategies based on the PEGylation (attachment of polyethylene glycol) may prolong the half-life time of staphylokinase, thereby improving its bioactivity in disease conditions (312).

Peptidyl Arginine Deiminase Inhibitors

Cl-amidine and F-amidine target all peptidyl arginine deiminase (PAD) isoforms were actively applied in many preclinical models to study NETosis. Various tumors are associated with the overexpression of PAD and increased citrullination. In 1958, Rogers and Simmonds were the first to describe protein citrullination in an animal protein as the process of converting peptidyl arginine into peptidyl citrulline. Since citrulline cannot be encoded in vivo, it only occurs after translation (313). Peptidyl arginine deiminases (PADs, also called PADIs) are an enzyme family which can convert protein arginine residues to citrulline in a Ca²⁺-dependent manner. This enzyme family comprises 5 isoforms (including PAD1, 2, 3, 4 and 6) which are highly conserved, have tissue-specific distribution and target substrates respectively (314).

PAD2-mediated histone citrullination is proposed as a potential therapeutic target for prostate and colon cancer (201, 315). PAD2 also regulates genes expression related to lactation through histone citrullination (316). The gonadotropin-releasing hormone (GnRH) agonist can stimulate PAD2-mediated histone H3 citrullination which epigenetically regulates the expression of gonadotropin genes such as luteinizing hormone β (LHβ) and follicle-stimulating hormone β (FSHβ) in gonadotropes (317). Recent studies have identified that PAD2 inhibition can reduce inflammatory cytokine production and NET formation in endotoxemia (318). PAD4-mediated citrullination promotes chromatin decondensation and DNA fragmentation, thereby affecting chromatin structure. PAD4 is critical for NET-mediated anti-microbial function (319). Furthermore, PAD4 can also regulate the transcriptional activity of p53 in tumor progression (320). Additionally, PAD4 promotes the metastasis of gastric tumors by regulating the expression of CXCR2, keratin K14 (KRT14) and TNFβ, which can accelerate angiogenesis, cell proliferation, migration and tumor immune microenvironment establishment (321). Inhibition of PAD4-mediated NETosis was also possible using an antagonist miR-155, which inhibits PAD4 mRNA synthesis and NET formation in response to PMA (322). In the experimental model of systemic lupus erythematosus, Cl-amidine treatment strongly inhibits NET-induced vascular damages, endothelial dysfunction and kidney injury. Inhibition of PAD4 also strongly decreased the expression of IFNγ, reduced proteinuria and immune complex attachment to the kidney tissues and in addition, protected from skin disease (323). Interestingly, PAD4-deficient mice had accelerated diabetic wound healing compared to wild-type mice (324). Although these irreversible inhibitors inactivate Ca²⁺-bound PAD4, they lack specificity and also interact with other isoforms of the PAD-family. Lewis et al., generated two reversible inhibitors GSK199 and GSK484 which are highly specific for PAD4 and can inhibit NETosis in murine and human neutrophils (325). Removal of NETs with DNAse I or pharmacological inhibition of PAD4 with GSK484 inhibitor prevent cancer-associated kidney injury in mice (326). However, in recent studies, GSK484 also enhanced irradiation-induced damages in triple-negative breast cancer cells, which subsequently had inhibitory effects on cell proliferation, migration and invasion (327). In mouse models of sepsis, deficiency of PAD4 or DNAse I treatment strongly reduced intravascular thrombin activity, inhibited platelet aggregation and improved microvascular perfusion (328). Patients with acute thrombotic microangiopathies displayed low plasma levels of DNAse I compared to the healthy subjects (329). In mouse models of HIT, genetic deficiency or GSK484-mediated inhibition of PAD4 abolishes thrombus formation (135). In vitro, DNAse I/GSK484 strongly inhibited the epithelial-mesenchymal transition-promoting ability of NETs in gastric cell cultures (87), indicating multiple effects of exogenous DNAse I in cancer.

Other effects may also result from PAD-mediated inhibition of ET formation. PAD1 and PAD3 target keratin K1, filaggrin and myelin, thus playing a specific role in epidermis differentiation (330). PAD enzymes are also positively associated with diffuse inflammation in the brain (331). In macrophages, PAD2 becomes activated due to increased levels of Ca²⁺ and can induce apoptosis by citrullinating vimentin (332). PAD2 citrullinates many proteins such as actin and vimentin in dendritic cells and dendritic cell-derived osteoclasts and in brain tissues (333, 334). Furthermore, overexpression of PAD2 in T cell line was shown to induce vimentin citrullination and apoptosis (335). Recently, PAD3 was found to be necessary for apoptosis-inducing factor (AIF)-mediated apoptosis in human neural stem cells (336). In comparison to other PAD family members, PAD4 has more catalytic substrates. PAD4 is involved in cell apoptosis and differentiation and deiminates nonhistone proteins such as p300, nucleophosmin (NPM1), an inhibitor of growth protein 4 (ING4) and Lamin C, which are involved in cell apoptosis or DNA damage (337). Moreover, PAD4-mediated citrullination participates in the regulation of human 40S ribosomal protein S2 (RPS2) and ribosome assembly (338). PAD4 targets collagen and decreases the adhesion of synovial fibroblasts and mesenchymal stem cells (339). DNA methyltransferase DNMT3A can be citrullinated by PAD4, which provides a novel mechanism for controlling de novo DNA methylation (340).

Cyclosporine A

Cyclosporine A suppresses immunocompetent T cells reversibly and is applied for the treatment of autoimmune diseases such as rheumatoid arthritis, and further viral, fungal and parasitical infections (341). Cyclosporine A binds to cyclophilin, thereby downregulating the nuclear factor of activated T cells (NFAT) signaling, thus further inhibiting the calcineurin pathway (342). Efficient induction of NETosis requires cytoplasmic Ca²⁺ increase, linking the cyclosporine A-induced calcineurin pathway to NETosis. IL8-induced NETosis is reduced by combining treatment of ascomycin and cyclosporine A (343), suggesting a possibility to develop a therapeutic approach of NETosis.

Heparin

Heparin is an anti-coagulant, extensively used in different therapies for the prevention of blood clotting during heart surgery, kidney dialysis, as well as for the treatment of VTE, heart attacks and angina (344). Heparin also inhibits many hallmarks of cancer, such as cancer cell survival, angiogenesis and migration (345). Moreover, heparin treatment can induce HIT, which is a life-threatening process, based on a severe immune reaction to heparin, characterized by thrombocytopenia and severe thrombosis. In patients with HIT, antibodies are produced against heparin-platelet factor 4 (PF4) complexes. Interestingly, this immune complex can directly activate neutrophils and enhance NET formation, which is sufficient for the development of thrombosis (135). PF4 binds to NETs, which renders NETs more compact. The complex then binds HIT antibodies, thereby protecting NETs from DNAse degradation (346). In the mouse model of HIT, inhibition of NET formation through PAD4 inactivation can reduce venous thrombus formation but not thrombocytopenia (346), suggesting that other alternative molecular mechanisms are involved in this process. HIT-induced NETosis is further enhanced by ROS production and NE. Interestingly, heparin derivatives, such as low molecular weight heparin, fondaparinux and heparan sulfate cannot induce profound NETosis (347). Altogether these results suggest that heparin induces neutrophil activation and NETosis contributes to venous thrombosis in HIT, which is triggered by PF4-NET-HIT antibody complexes.

The effects of unfractionated heparin, low-molecular-weight heparin (LMWH), e.g., parnaparin and non-anti-coagulant heparin were studied in histone-induced diseases. Heparin was able to protect mice and rats from organ and tissue damage, as well as death by antagonizing histones in the blood (348–351). In a mouse model of sepsis, heparin pretreatment could significantly decrease the level of NETs in serum and lung tissues (352). NET formation promotes cancer cell migration, invasion and angiogenesis, which were inhibited by heparin or other histone-binding agents (16). NETs also contributed to a variety of cancer or cancer-associated thrombosis (97). LMWH is currently the preferred treatment for prophylaxis and cancer-associated thrombosis (353). However, more experimental evidence is necessary to understand the effects of heparin in NET formation of cancer patients. Heparin derivatives may be a promising tool to cure diseases with high levels of plasma histones, thereby potentially inhibiting NETosis without dramatic changes in hemostasis.

Metformin

Metformin was originally used in diabetic patients to normalize blood glucose levels. The anti-diabetic effects of metformin are due to the inhibition of hepatic gluconeogenesis, which is possibly associated with an insulin-mediated increase in glucose uptake in skeletal muscle cells (354). Metformin acts by inducing adenosine monophosphate-activated kinase (AMPK), an enzyme regulating energy metabolism through activation of glucose or oxidation of fatty acids (355). High glucose and hyperglycemia increase the release of NETs and circulating markers of NETosis, respectively (356). Although metformin inhibited NETosis in vitro by reducing proteinase-3, histones and extracellular DNA, it did not affect insulin synthesis. In neutrophils, metformin prevented membrane translocation of PKCβII and activation of Nox, thereby decreasing NETosis in response to PMA and Ca²⁺. In line with this, metformin also decreased NET components in the plasma of patients with type 2 diabetes before and after treatment with insulin or dapagliflozin (357).

Circulating neutrophil levels are often increased in patients with a polycystic ovarian syndrome which is associated with an increased risk to develop ovarian cancer (358–360). Ibanez et al., reported that metformin can reduce neutrophil count in polycystic ovarian disease (360). These studies support the idea that metformin can prevent the increased neutrophil levels and NETosis that are associated with aggressive forms of ovarian cancer.

NET-independent mechanisms of metformin have also been observed. Metformin could impair tumor growth when administered during fasting-induced hypoglycemia. The anti-tumor effects of metformin were mediated by glycogen synthase kinase 3β (GSK3β) activation and PP2A-B56δ complex formation (361). Metformin inhibited the growth of a variety of breast cancer cells by inducing cell cycle arrest and apoptosis (362). Similar to other cell lines, metformin also induces AMPK activation, reduced the phosphorylation of epidermal growth factor receptor (EGFR), mitogen activated protein kinases (MAPKs) and Src and lowered the levels of cyclins D1 and E in breast cancer cells (362). Metformin also inhibits signal transducer and activator of transcription 3 (STAT3) activation and thereby reduced cell proliferation (363). Furthermore, metformin also activates p53 by activating AMPK, ultimately stopping the cell cycle (357, 364).

Metformin inhibits the proliferation of breast cancer cells with aberrant expression of human epidermal growth factor receptor 2 (HER2). Translational suppression of HER2 expression was observed after metformin treatment and this effect was triggered by the inhibition of the mTOR-S6K1 signaling pathway (365). Besides breast cancer, metformin can inhibit the proliferation of prostate, endometrial and brain cancer cells. Similar effects induced by metformin, inducing cell cycle arrest and suppressing the mTOR signaling pathway (366–368). In vivo experimental conditions, metformin treatment significantly reduced the primary tumor size of mammary adenocarcinomas and prolonged the lifespan of MMTV–Her2/Neu mice (369). Heterozygote mice of the tumor suppressor gene PTEN develop tumors in different organs, and metformin delayed tumor onset by 25% (370).

Many inhibitory effects of metformin on tumor growth through AMPK and mTOR signalings were confirmed using different mouse models of cancer (371–375). Metformin was also effective in reducing the growth of intestinal polyps in tumor suppressor Apc-mutant mice (376) by reducing mTOR/S6K/S6 signaling in the epithelium of the intestine. Of note, in this intestinal tumorigenesis model, tumor growth was shown to be associated with increased neutrophil infiltration and NETosis (130), raising the possibility that metformin may also inhibit NET-dependent tumor growth.

Although numerous preclinical, clinical and epidemiological studies proposed that metformin treatment inhibits tumor growth compared to other hypoglycemic treatments, it is still an open question whether metformin can be a potential candidate for the treatments of cancers predisposing tumor microenvironment to the release of ETs.

Thrombomodulin/Activated Protein C Complex

Thrombomodulin is an endothelial receptor, playing an important role in vascular homeostasis and regulation of coagulation. Thrombomodulin forms a complex with thrombin, thereby inactivating the coagulant activity of thrombin which activates protein C and thrombin activatable fibrinolysis inhibitor (TAFI) (377). Besides thrombin, thrombomodulin also regulates the inactivation of complement 3b (378). Recombinant thrombomodulin is given to the patients with disseminated intravascular coagulation, thereby protecting them from tissue injury (379). Recombinant thrombomodulin neutralizes damage-associated molecular patterns (DAMPs), including histones and HMGB1, inhibits aberrant activation of the complement system, protecting the endothelium (380). Using in vitro platelet-neutrophil coculture models, Shimomura et al., demonstrated that recombinant thrombomodulin may inhibit LPS-induced NETosis (381). Later, Helms et al. found that treatment of rats with recombinant thrombomodulin during septic shock limits excessive neutrophil activation and rescues a balanced coagulation and immunothrombosis response (382). This promising therapeutic tool would be important to follow in the future using mouse models of cancer.

Activated protein C (APC) is a serine protease with anti-coagulant and anti-inflammatory effector functions. Activation of the blood coagulation cascade by TF induces thrombin generation and the formation of a fibrin network. In addition, thrombin binds to thrombomodulin, and activates protein C in complex with endothelial protein C receptor (EPCR). Zymogen protein C is cleaved by thrombin to generate functionally active APC. After protein cleavage, APC forms a complex with protein S, and inactivates coagulation factors (Va, VIIIa) and as a negative feedback loop, inhibits thrombin generation (383). Therefore, long-term APC treatment could potentially increase the risk of bleeding complications (384). Besides this function, APC binds and activates PAR1 thereby enhancing vascular barrier integrity through sphingosine-1-phosphate receptor 1 (S1P1)-VE-cadherin signaling (385, 386).

The anti-inflammatory effects of APC involve the inhibition of neutrophil activation, NET formation and cell death. APC can effectively inhibit PI3K-PKC-dependent NET formation and this process is strongly dependent on the functional crosstalk between the macrophage-1 antigen (Mac-1), EPCR, and protease-activated receptor 3 (PAR3). APC can cleave PAR3 at a different site than thrombin, thereby inhibiting NET formation. Consequently, antibodies of EPCR, PAR3 and Mac-1 can reverse APC-mediated inhibition of NETosis (387).

Due to the multiple roles of APC in hemostasis and inflammation, it is difficult to predict the positive or negative effects of APC treatment in cancer progression. Increased levels of APC in the blood may limit metastasis by protecting the vascular barrier through VE-cadherin, but it may stimulate the metastatic potential of cancer cells (386). It has been shown that APC signaling enhances cancer cell migration, invasion and angiogenesis and also inhibits apoptosis (386, 388, 389). APC treatment could enhance breast cancer cell invasion in a dose-dependent manner (389). Cancer patients require long-term APC treatment which may induce severe bleeding complications (386), due to the hemostatic effects of APC on thrombin generation and factor Va/VIIIa functions. Although APC has a strong anti-inflammatory potential for the treatment of human patients, it is necessary to test recombinant mutant forms of APC with selective anti-inflammatory function in experimental models of cancer, without affecting thrombin generation and hemostasis.

Diphenyleneiodonium Chloride

Diphenyleneiodonium chloride (DPIC) is a hypoglycemic agent, identified as an inhibitor of NADH/Nox with highly potent anti-microbial activity against Mycobacterium tuberculosis and Staphylococcus aureus (390, 391). However, DPIC can also inhibit nitric oxide synthase (392), xanthine oxidase (393) and NADPH cytochrome P450 oxidoreductase (394), thereby inhibiting ROS production. Furthermore, DPIC inhibits oxidative phosphorylation (OXPHOS) and consequently reduces ATP production, thereby switching energy production to the lactic acid energy system (390). DPIC treatment strongly inhibits mitochondria function, thus leading to metabolic senescence (395). Interestingly, the effects of short-term DPIC treatment on cancer cells were independent of p53. However, long-term treatment showed that p53 expression facilitates a prolonged cell cycle arrest and protects cancer cells from apoptosis, while p53 deficiency could induce apoptosis with poly ADP-ribose polymerase (PARP) cleavage and DNA fragmentation in cancer cells (396). Altogether, these results suggest that DPIC treatment can reduces tumor growth by the inhibition of cancer cell proliferation and activation of the immune system through factors secreted by senescent cancer cells.

DPIC inhibits extracellular DNA release in PMA-stimulated neutrophils, although the degree of DPIC-inhibited NET formation was strongly dependent on the dose of external stimuli (49, 80). In different lung epithelial cells, NET formation is significantly increased by the secretion of CXCL8, IL8 and IL6 and this process was inhibited by DPIC (397). In the model of in vitro cigarette smoke extract-induced NETosis, DPIC treatment also inhibited this process (398). In mice, tobacco smoke increases lung metastasis by sustaining lung inflammation and thereby inducing NETosis which subsequently awake dormant cancer cells (108). Further investigation is necessary to show the effects of DPIC in long-term treated tumors and tumor microenvironment in vivo, focusing on the context of mitochondria dysfunction and senescence, as well as the distribution of NETs in cancer and lung metastasis.

High Mobility Group box-1 Antagonists

High mobility group box-1 (HMGB1) is a nonhistone chromatin-associated protein, and as a nuclear cofactor in transcription regulation, interacting with many transcription factors and histones, supporting gene expression in the cells (399). However, HMGB1 is also secreted into the extracellular milieu, thereby initiating several interactions with receptors on the cell surface or with extruded DNA, triggering various signaling mechanisms and NETosis (399, 400). HMGB1 has a cytokine-like activity, thus regulating immune cell functions, including chemotaxis and immune modulation (401). In monocyte/macrophage-infiltrating disease conditions, HMGB1 facilitates macrophage reprogramming towards a proinflammatory phenotype through TLR4 activation (402). Interestingly, exposure to HMGB1 strongly increases the amount of extracellular DNA and citrullinated histone 3 in wild-type neutrophils, however, this effect was not observed in TLR4-deficient neutrophils (403). In mouse models treated with LPS, HMGB1 antibody treatment could decrease the levels of citrullination of histone 3 (403). Altogether, these results suggest that HMGB1 is a potential target for the development of anti-inflammatory therapies against TLR4-mediated NETosis.

Interestingly, metformin as a potential inhibitor of NETosis directly binds to the C-terminal tail of HMGB1 (357, 404). In the acute liver damage model, HMGB1 was released from damaged liver cells and metformin treatment could inhibit this process, protecting the liver cells (404). In another mouse model, metformin can significantly inhibit HMGB1 secretion and consequently reduce LPS-induced macrophage inflammatory responses, thereby improving the survival of endotoxemic mice (405). Altogether, these results suggest that metformin would be a potential drug to inhibit HMGB1-induced inflammation and NETosis.

Platelets are the major reservoirs of HMGB1, and it is released by activated platelets (400). HMGB1 binds TLR4 receptors on the platelet surface, thereby inducing recruitment of myeloid differentiation primary response 88 (Myd88) and guanylyl cyclase to the plasma membrane, leading to the activation of cGMP-dependent protein kinase I (400, 406). In a mouse model lacking HMGB1 in platelets, decreased thrombosis, lung inflammation and NETosis were observed indicating pleiotropic effects of HMGB1 in thromboinflammation (406).

Cancer cell-derived HMGB1 can modulate platelet-resident TLR4 receptors, thereby increasing platelet-dependent tumor metastasis. Although NETosis was not addressed in this study, blocking HMGB1 function in tumor cells was effective to inhibit tumor metastasis (407). HMGB1 is also expressed in keratinocytes. HMGB1-deficient keratinocytes displayed a marked reduction in NET formation, and subsequently delaying wound healing and promoting tumorigenesis in mice (408). Using anti-HMGB1 antibody treatment, HMGB1-mediated NETosis was strongly inhibited (403). It is tempting to investigate whether HGMB1 may also trigger DNA release from other inflammatory immune cells in proinflammatory tumor microenvironment.

Purinergic P2Y12 Receptor Blockers

Purinergic P2Y12 receptor (P2Y12) blockers (clopidogrel, ticagrelor, cangrelor, prasugrel) are widely used in patients with cerebrovascular, coronary artery, cerebrovascular and peripheral vascular diseases (409). The thienopyridine-derived metabolite irreversibly inhibits the binding of ADP to the receptor P2Y12, resulting in decreased platelet activation and aggregation responses, and reducing inside-out activation of platelet integrin αIIbβ3 integrin (410). Neutrophil-mediated platelet activation was suggested to be dependent on ADP (411, 412), therefore ADP blockers consequently attenuate platelet-neutrophil interactions and NETosis. In a mouse model of cholesterol crystal embolism, extracellular DNA has been exposed from NETs and damaged endothelium and activated platelets from emboli and vascular occlusion, leading to tissue infarction and kidney injury (231). In this model, P2Y12 blockade similarly to the DNAse I treatment strongly inhibited platelet function, consequently inhibiting extracellular DNA release and associated ischemia and organ injury (231).

In ST-elevation myocardial infarction (STEMI), the interaction between platelets and neutrophils results in the secretion of polyP in the presence of thrombin (413). In the infarct-related arteries, platelets release polyP, stimulating neutrophils to form thrombogenic/TF-bearing NETs (414, 415). Although ticagrelor significantly inhibited the NETotic effect of coronary stents in vitro, this did not rely on the P2Y12 receptor. These results indicated that ticagrelor may have pleiotropic effects on NETosis independently of platelets (415). The pancreatic cancer microenvironment is highly rich in tumor-associated neutrophils, platelets and NETs (416). Clopidogrel was shown to inhibit cancer growth and metastasis in PANC02 pancreatic cancer model (417). In the future, it will be important to analyse the effect of P2Y12 blockers on cancer-associated neutrophil activation and NETosis.

Disulfiram

Disulfiram inhibits aldehyde dehydrogenase and is used to treat alcohol dependence (418). Disulfiram is also a potent inhibitor of gasdermin D in mouse and human macrophages and neutrophils (419, 420). Gasdermin D is a pore-forming protein playing a pivotal role in inflammatory cell death (419). In macrophages, inflammasome activation by canonical and or non-canonical pathways induces the cleavage of gasdermin D, which translocates to the plasma membrane thereby forming pores and inducing pyroptosis (421). In neutrophils, cytoplasmic caspase was shown to be directly activated by LPS or gram-negative bacteria independently of TLR4 (422). A recent study by Silva et al., showed that during sepsis caspase-11 activation induces gasdermin D cleavage, resulting in NET formation (420). Besides these mechanisms, gasdermin D cleavage is also generated by NE, which is released from neutrophils upon activation (423). Interestingly, inhibition of gasdermin D with disulfiram abolished NET formation reducing multiple organ dysfunction and sepsis-associated lethality (420). These studies indicate that disulfiram could be an important therapeutic agent to target gasdermin D, thereby preventing organ injury.

Diethylcarbamazine

Diethylcarbamazine (DEC) is a derivate of piperazine, used as an anti-parasitic drug (424). Although at low doses DEC improves cytokine production, a high dose of this drug increases the respiratory burst in neutrophils (425). In vivo, DEC reduces the inflammatory granuloma formation in a bacterial infection model (426). DEC also decreases NET formation of neutrophils isolated from healthy subjects upon in vitro activation with PMA (427). In a follow-up study, DEC in both healthy donors and diabetes mellitus type 2 patients displayed an immunomodulatory effect inhibiting and delaying the tendency toward NET formation by their neutrophils (428). DEC in addition to inhibiting NETosis, also inhibits COX2, NF-kB activation, iNOS, TNFα and IL1β (429), indicating that the effects of DEC can be associated with many immunomodulatory pathways.

Glucuronoxylomannan

Glucuronoxylomannan (GXM), a polysaccharide, represents the main capsular content of the opportunistic yeast Cryptococcus neoformans, which has potent immunosuppressive properties. In a mouse model of rheumatoid arthritis triggered by collagen type II, GXM could improve the disease severity, by downregulating the cytokine and growth factor (TNFα, IL1β, IL6 and TGFβ) levels, thereby inhibiting Th17 cell differentiation and subsequent IL17 secretion (430). Furthermore, Rocha et al., showed that GXM treatment could abolish NET formation, independently of the agonist and stimuli (431). Future studies are required to validate whether GXM could be a potential therapeutic tool in ET-mediated thromboinflammation and cancer triggered by various cell types.

Anti-Citrullinated Antibodies

Anti-citrullinated protein antibodies (ACPAs), produced against citrullinated proteins, are diagnostic and prognostic markers of rheumatoid arthritis (432). Recent studies also provided evidence for circulating autoantibodies against citrullinated tumor-associated proteins in breast cancer patients (433). Anti-citrullinated proteins specifically targeting citrulline at histone 2A and 4 positions were proposed as a direct approach to inhibit murine and human NET formation (434).

Conclusion

Research studies during the last decade provided important progress on better understanding of the pathophysiological role of ETs ( Table 1 ). Neutrophils release ETs in response to proinflammatory stimuli and tumor cell and tumor microenvironment. Cancer-mediated NETosis also induce thrombosis, which leads to multiple organ failure. Dissolution of NET structures by DNAse I may represent benefits, but side-effects of such treatment may also result in secondary immune responses and procoagulant environment triggered by disseminated NET fragments circulating in the body. Increasing experimental and clinical evidence indicates the multiple sources of ETs in different pathological contexts, such as intestinal inflammation, sepsis, thrombosis, autoimmune diseases and diabetes. The proinflammatory and proangiogenic landscape of tumor microenvironment can potentially trigger activatory signaling pathways of ET formation, in different immune cells, including eosinophils, dendritic cells, monocytes, macrophages, basophils and lymphocytes. So far, only limited experimental and clinical evidence is available to link non-neutrophil ETs to the cancer progression and response to the anti-cancer therapies. Therefore, studies evaluating localization of extracellular DNA and traps, including immunohistological detection of colocalized cell-lineage-derived proteins, citrullinated histones, detection of extracellular DNA and traps in serum and blood samples using flow cytometry are of paramount importance. The analysis of citrullinome signature associated with immune response and response to anti-cancer treatments may offer potential diagnostic and prognostic approaches. Understanding the underlying mechanisms of ETosis in cancer and grasping the impact of nucleases, anti-thrombotic, anti-diabetic, anti-malaria and immunosuppressive drugs on ETs may help to interconnect treatment strategies between several disease contexts and propose new therapeutic modalities for the prevention and treatment of cancer.

Table 1.

Pathophysiological role of ETs in cancer.

Biological effect	ET type	Cancer model	Underlying mechanism	Ref.
Tumor growth	NETs	Colorectal cancer In vitro: DKs-8, DKO-1 cells In vivo: Apc-KRAS^G12D mouse model	Cancer cells transfer KRAS mutations through exosomes to neutrophils and induce neutrophil recruitment and NETosis via upregulation of IL8, promoting cancer cell proliferation.	(96)
		Colorectal cancer In vitro: MC38 cells In vivo: syngeneic subcutaneous MC38 cancer model	NET-associated PD-L1 induces T cell exhaustion and enhances tumor growth.	(109)
		Hepatocellular carcinoma In vivo: DEN-HFCD, STAM mouse models	NETs enhance differentiation of regulatory T cells by promoting mitochondrial oxidative phosphorylation in naive CD4+ T cells via TLR4, amplifying tumor burden.	(110)
Migration, Invasion; EMT	NETs	Breast cancer In vitro: MCF7 cells	NETs enhance the expression of EMT markers ZEB1, Snail and fibronectin, cancer stem cell marker CD44, proinflammatory mediators, such as IL1β, IL6, IL8, CXCR1, MMP2 and MMP9.	(86)
		Gastric cancer In vitro: AGS cells	NETs enhance cancer cell migration and induce EMT; downregulation of E-cadherin and upregulation of vimentin expression.	(87)
		Pancreatic cancer In vitro: BxPC3, MIA, PaCa2, PANC1 cells In vivo: subcutaneous MIA and PaCa2 xenograft cancer models Ex vivo: human PDAC	Release of IL1β during NETosis activates EGFR/ERK pathway, leading to the EMT; downregulation of E-cadherin and upregulation of Snail, N-cadherin and vimentin expression.	(88)
		Colorectal cancer In vitro: DKs-8, DKO-1 cells In vivo: Apc-KRAS^G12D mouse model	KRAS mutant exosomes from tumor cells induce NETosis via IL8, leading to the enhanced cancer cell migration and invasion.	(96)
		Breast cancer In vitro: 4T1, 4T07, BT-549 and C3(1)-Tag cells	Cancer cell-derived G-CSF primes neutrophils, resulting in lytic NETosis; cathepsin G enhances NET-mediated cancer cell invasion among other NET-associated proteins.	(14)
		Pancreatic cancer In vitro: AsPC-1 cells	NETs induce cancer cell migration via TLR2 and TLR4.	(16)
	METs	Colon cancer In vitro: HCT116 and SW480 cells Ex vivo: human colon cancer	Cancer cells promote MET formation via PAD2; METs interact with tumor cells and enhance tumor cell invasion.	(201)
Metastasis	NETs	Breast cancer In vitro: 4T1 series, AT3, MDA-MB-231 and sublines In vivo: syngeneic orthotopic (4T1 series, AT3), xenograft (MDA-MB-231 and sublines) cancer models Ex vivo: human breast cancer	Tumor-derived cathepsin C (CTSC) triggers CTSC-PR3-IL1β axis in neutrophils, upregulating IL6 and CCL3 synthesis. CTSC-PR3-IL1β induces ROS production and NET formation which degrade thrombospondin-1, thereby supporting metastatic growth of lung cancer cells.	(95)
		Breast cancer In vivo: 4T1 experimental and spontaneous breast cancer metastasis models	NETs enhance lung metastasis.	(14)
		Breast cancer and colon cancer In vitro: MDA-MB-231, MCF-7 and HCT116 cells In vivo: syngeneic (4T1) and xenograft (MDA-MB-231) orthotopic and intrasplenic (MMTV-PyMT mice and E0771 cells) cancer models Ex vivo: human breast and colon cancer	CCDC25 on cancer cell surface acts as a sensor and binding partner for NET-DNA; binding leads to activation of ILK–β-parvin–RAC1–CDC42 cascade, cytoskeleton remodeling and formation of distant metastases.	(18)
		Breast cancer In vitro: D2.0R, MCF7 cells In vivo: syngeneic (D2.0R) and xenograft (MCF7) experimental breast cancer metastasis models	NET-associated NE and MMP9 cleave laminin and degrade thrombospondin-1 leading to the activation of integrin α3β1 and FAK/ERK/MLCK/YAP signaling, resulting in reactivation of dormant cancer cells during tumor metastasis.	(108)
		Colon, melanoma, lung and breast cancer In vitro: primary melanoma and LS174T, HT29 cells In vivo: syngeneic subcutaneous (4T1, LLC and HT29) and intradermic (B16OVA and 4T1) cancer models	Cancer cells trigger NETosis by CXCR1 and CXCR2 activation; NETs protect tumor cells from contact with cytotoxic T cells and NK cells, promoting cancer cell dissemination and lung metastasis.	(105)
		Lung cancer In vitro: A549 cells In vivo: experimental liver metastasis of A549 cells (intrasplenic injection into caecal ligation and puncture-induced sepsis model)	Tumor- and NET-derived β1-integrin mediates adhesion of NETs to circulating tumor cells, facilitating cancer cell adhesion to the liver sinusoids.	(102)
		Ovarian cancer In vitro: ES2 and ID8 cells In vivo: syngeneic (ID8) and xenograft (ES2), (intrabursal and intraperitoneal injection) cancer models	Cancer-derived cytokines (IL8, G-CSF, GROα, GROβ) promote NETosis; NETs accumulate in premetastatic niche and enhance the formation of omental metastases.	(20)
	METs	Colon cancer In vivo: MC38 experimental colon cancer metastasis model Ex vivo: human colon cancer	Cancer cells promote MET formation via PAD2, enhancing the formation of liver metastases.	(201)
Cancer-associated thrombosis	NETs	Chronic myelogenous leukemia (CML), breast and colon cancer In vivo: syngeneic orthotopic breast (4T1) and subcutaneous lung (LLC) and CML mouse models	Cancer cells predispose neutrophils to form NETs via G-CSF, promoting microthrombosis in the lung.	(97)
		Breast cancer In vivo: syngeneic orthotopic breast (4T1 and 67NR) models	Cancer-derived G-CSF induces neutrophilia and NETosis, leading to the prothrombotic phenotype.	(113)
		Glioma Ex vivo: human glioma	Platelets of late-stage glioma patients induce NETosis via P-Selectin and NETs promote hypercoagulant state and thrombogenicity in endothelial cells.	(125)
		Myeloproliferative neoplasms (MPN) In vivo: Jak2^V617F mouse model Ex vivo: human MPN	Jak2 ^V617F mutation stimulates NET formation and thrombosis in a PAD4-dependent manner.	(132)
		Pancreatic cancer In vitro: AsPC-1 cells Ex vivo: pancreatic and biliary cancer	Tumor cells induce NET generation in a cAMP- and thrombin-dependent, and ROS-independent manner; NETs enhance thrombin generation.	(16)
		Pancreatic cancer Ex vivo: orthotopic (Panc02) cancer model, human pancreatic cancer	NETs induce RAGE-dependent platelet aggregation and increase TF expression, thereby enhancing coagulation.	(127)
		Pancreatic cancer In vitro: AsPC-1 cells	Platelets primed by tumor cells induce rapid NET generation; NETs trap platelets and stimulate thrombus formation under shear conditions.	(128)
		Small intestine cancer In vivo and ex vivo: Apc^Min/+ mouse model	Inflammation-associated complement activation via neutrophil C3aR induces NETosis, hypercoagulation, and N2 neutrophil polarization in small intestine.	(130)
		Ex vivo: human solid cancers Prostate, liver, lung, bladder and breast	Malignant tumors enhance NETosis via G-CSF, inducing microthrombosis and the occurrence of ischemic stroke with elevated troponin levels.	(134)
Secondary organ damage	NETs	Breast cancer and insulinoma In vivo: MMTV-PyMT and RIP1-Tag2 transgenic models	Cancer cell-derived G-CSF induces systemic NETosis. NETs occlude kidney and heart vessels, inducing irregular blood flow, increased endothelial cell activation with upregulated expression of proinflammatory mediators, ICAM1, VCAM1, E-selectin, IL1β, IL6, and CXCL1.	(98)
Poor prognosis and therapeutic resistance	NETs	Bladder cancer In vitro: MB49, UM-UC3 cells In vivo: syngeneic heterotopic MB49 bladder cancer model Ex vivo: human bladder tumor	Radiation induces HMGB1 release in tumor microenvironment, triggering NETosis through TLR4; NETs enhance resistance to radiotherapy by suppressing CD8+ T cell infiltration.	(111)
	NETs, METs	Ex vivo: human pancreatic neuroendocrine tumors	Poor prognosis and postoperative recurrence of resected tumors.	(200)
	NETs,EETs	Ex vivo: human classic Hodgkin lymphoma, nodular sclerosis subtype	Eosinophilia and detection of NETs and EETs in lymph tumor tissues. Correlation between NET formation and fibrosis High expression of PAR-2 and nuclear p-ERK in cancer cells. Enhanced TF expression and procoagulancy in tumor-associated endothelium.	(160)

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EMT, epithelial-mesenchymal transition; DEN-HFCD, diethylnitrosamine + choline-deficient, high-fat diet; STAM, Stelic Animal Model; MMTV-PyMT, mouse mammary tumor virus-polyoma middle tumor-antigen.

Author contributions

MM and EM-B wrote the manuscript. AP, CH and AB contributed to the writing and drafted the figures. H-JA and TG critically reviewed the manuscript and contributed to the writing. All authors contributed to the article and approved the submitted version.

Funding

This work was supported by the Bayerisches Landesamt für Gesundheit und Lebensmittelsicherheit (BLGL), project number 15-25, Deutsche Forschungsgemeinschaft, CRC TRR152/P15, AN372/14-4 and AN372/30-1 and Förderprogramm für Forschung und Lehre (FöFoLe), LMU, Munich, Germany. MM, AP and CH were recipients of a fellowship from FöFoLe, 2020-2022, BLGL and CSC (China Scholarship Council), respectively.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s Note

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PERMALINK

Extracellular DNA Traps: Origin, Function and Implications for Anti-Cancer Therapies

Medina Mamtimin

Akif Pinarci

Chao Han

Attila Braun

Hans-Joachim Anders

Thomas Gudermann

Elmina Mammadova-Bach

Abstract

Introduction

Neutrophil Extracellular Traps

Molecular Mechanisms of Neutrophil Extracellular Trap Formation

Tumor-Associated NETs

Figure 1.

Cancer-Associated Thromboinflammation and NETosis

Eosinophil Extracellular Traps

Figure 2.

Dendritic Cell Extracellular Traps

Figure 3.

Monocyte and Macrophage Extracellular Traps

Figure 4.

Figure 5.

Mast Cell Extracellular Traps

Figure 6.

Basophil Extracellular Traps

Figure 7.

T Cell Extracellular Traps

Figure 8.

B Cell Extracellular Traps

Other Sources of Extracellular DNA

Endothelial Cell-Derived Extracellular DNA

Platelet-Derived Extracellular DNA

Cardiomyocyte-Derived Extracellular DNA

Tumor Cell-Derived Extracellular DNA and Horizontal Transfer of DNA

Endogenous DNAse

Exogenous DNAse I

Other Pharmacological Approaches

Aspirin

Prostaglandin E2

Chloroquine

Staphylokinase

Peptidyl Arginine Deiminase Inhibitors

Cyclosporine A

Heparin

Metformin

Thrombomodulin/Activated Protein C Complex

Diphenyleneiodonium Chloride

High Mobility Group box-1 Antagonists

Purinergic P2Y12 Receptor Blockers

Disulfiram

Diethylcarbamazine

Glucuronoxylomannan

Anti-Citrullinated Antibodies

Conclusion

Table 1.

Author contributions

Funding

Conflict of Interest

Publisher’s Note

References

ACTIONS

PERMALINK

RESOURCES

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