Roles of Microvesicles in Tumor Progression and Clinical Applications

Abstract

Microvesicles are extracellular vesicles with diameter ranging from 100 to 1000 nm that are secreted by tumor cells or other cells in the tumor microenvironment. A growing number of studies demonstrate that tumor-derived microvesicles are involved in tumor initiation and progression, as well as drug resistance. In addition, tumor-derived microvesicles carry a variety of immunogenic molecules and inhibit tumor response to immunotherapy; therefore, they can be exploited for use in tumor vaccines. Moreover, because of their high stability, tumor-derived microvesicles extracted from body fluids can be used as biomarkers for cancer diagnosis or assessment of prognosis. Tumor-derived microvesicles can also be deployed to reverse drug resistance of tumor regenerative cells, or to deliver chemotherapeutic drugs and oncolytic adenovirus for the treatment of cancer patients. This review summarizes the general characteristics of tumor-derived microvesicles, focusing on their biological characteristics, their involvement in tumor progression, and their clinical applications.

Introduction

Extracellular vesicles (EVs) are a heterogeneous collection of cell-derived membranous structures¹ that can be divided into four types: microvesicles (MVs), exosomes, oncosomes, and apoptotic bodies.^2,3 MVs are produced via shedding from the plasma membrane and have diameters ranging from 100 to 1000 nm.^1,4 MVs are also known as ectosomes, microparticles, or shedding vesicles.^5,6 The proteins carried by MVs include CD40, β1 integrins, matrix metalloproteinases (MMPs), ADP-ribosylation factor 6 (ARF6), and Rho family members.^7,8 MVs are secreted into body fluids and have key roles in disease development and progression via regulation of intercellular signaling and intracellular communication.⁹

Tumor-derived MVs (TMVs) are MVs released by tumor cells in the tumor microenvironment (TME).^10,11 Components of the TME are closely related to tumor homeostasis, for example, tumor cells, immune and inflammatory cells, cancer-associated fibroblasts (CAFs), and extracellular matrix (ECM) components.^12,13 TMVs can be absorbed by cells in the TME, such as CAFs, and have an influence on target cell behavior. They can also interact with the ECM by promoting its degradation, thereby facilitating cancer cell migration and invasion. Once shed, TMVs modulate tumor characteristics and activities including tumor invasion, metastasis, angiogenesis, drug resistance, and immunomodulation.¹⁴ Furthermore, TMVs can transfer bioactive contents including soluble factors, oncoproteins, chemokine receptors, oncogenes, transcripts of proteins, and microRNAs (miRNAs); thus, they are closely related to tumor development and progression.¹⁵ Moreover, TMVs are used in tumor vaccines to carry various immunogenic molecules to targeted tumor cells.¹⁶ Accumulating evidence indicates that TMVs could be used to deliver cancer therapeutics, including chemotherapeutic drugs and oncolytic adenoviruses. Overall, these results suggest that TMVs could represent novel mediators of oncogenesis, as well as having potential clinical applications.¹⁷

The Biogenesis and Characterization of MVs

The Biogenesis of MVs

MVs were first discovered in the 1970s in cell lines derived from a male patient with Hodgkin’s disease.¹⁸ Subsequently, in the 1980s, Poste et al¹⁹ found that MVs spontaneously secreted by highly metastatic B16 mouse melanoma (F10). Once the MVs had fused with weakly metastatic B16 mouse melanoma cells (F1), they could increase the proficiency of F1 cells to metastasize to the lung. This pioneering research on MVs laid a solid foundation for numerous future studies, which have demonstrated the crucial parts played by MVs (through their molecular cargos) in immunomodulation and tumor progression.¹⁴ It is now well accepted that MVs originate from outward budding and fission of the cell membrane and are widely distributed in multiple body fluids, including urine, peripheral blood, and peritoneal effusions (Figure 1). The functions and components of MVs are associated with their cells of origin, which include tumor cells, stem cells, immune cells, and endothelial progenitor cells.²⁰ Interestingly, the abscission process is related to molecular rearrangements of the plasma membrane, which are affected by protein and lipid composition as well as Ca²⁺ levels.⁷

Figure 1.

Biogenesis and cargos of MVs. Extracellular vesicles include microvesicles (MVs), exosomes, oncosomes, and apoptotic bodies. MVs are produced via shedding from the plasma membrane and have diameters ranging from 100 to 1000nm. Increased intracellular Ca²⁺ can activate Ca²⁺-dependent enzymes, leading to depolymerization of the actin cytoskeleton and membrane remodeling, then promotion of MV shedding. Representative cargos of MVs are shown: P-gp, TF, EGFR, v-SNARE, ARF6, chemokine receptor, IL-6, IL-1β, VAMP-3, Ezrin, CD40, uPA, DNA, microRNA, tTG, EMMPRIN, MMPs, and VEGF.

Abbreviations: TF, tissue factor; EGFR, epidermal growth factor receptor; v-SNARE, vesicular soluble N-ethylmaleimide-sensitive factor attachment protein receptor; ARF6, ADP-ribosylation factor 6; IL-6, interleukin 6; IL-1β, interleukin 1β; VAMP-3, vesicle-associated membrane protein 3; CD40, cluster of differentiation 40; uPA, urokinase plasminogen activator; tTG, tissue-type transglutaminase; EMMPRIN, extracellular matrix metalloproteinase inducer; MMPs, matrix metalloproteinases; VEGF, vascular epithelial growth factor.

An increase in intracellular Ca²⁺ leads to alterations of the asymmetric phospholipid distribution of the plasma membrane. Phosphatidylserine and phosphatidylethanolamine are located on the inner side of the cytomembrane.²¹ The asymmetry is maintained by Ca²⁺-dependent enzymes including aminophospholipid translocases, flippases and floppies, and calpain.²² Increased intracellular Ca²⁺ levels or release of Ca²⁺ by the endoplasmic reticulum can activate Ca²⁺-dependent enzymes, leading to the inhibition of translocases and activation of scramblase. As a result, phosphatidylserine and phosphatidylethanolamine are not returned to the inner side of the membrane, and the actin cytoskeleton remains depolymerized, promoting MV shedding.^23,24

The degradation of MVs is controlled by small GTPases, including ADP-ribosylation factors (ARFs),²⁵ Rab22a²⁶ (also known as Rab22),²⁷ and Rho.²⁸ For example, ARF6 is a member of the ARF family of small GTP-binding proteins,¹⁰ and its activation is relevant to MV recycling and actin remodeling in the peripheral layer of cells.^29,30 Notably, activation of ARF-GTP also occurs in TMVs. In addition, myosin light-chain kinase (MLCK) can promote the production of MVs via MLCK-mediated myosin II light chain (MLC) phosphorylation. MLCK, a Ca²⁺/calmodulin dependent kinase, can promote the contraction of the actin-based cytoskeleton via MLC phosphorylation.³¹ The activation of ARF6 can promote the activation of MLCK via phospholipase D and extracellular signal-regulated kinase (ERK), contributing to the production of MVs.^25,28,32 However, MV shedding is blocked by MLC phosphorylation, in a process mediated by protein kinase C and ARF-6-GDP.²⁵ Rab22a has also been implicated in the formation of MVs²⁶ and is associated with ARF6-regulated MVs trafficking.³³ For example, the activation of Rab22a increased the production of MVs in breast cancer. Interestingly, Rab22a knockdown decreased hypoxia-induced generation of MVs but had only a slight effect on MV biogenesis under non-hypoxic conditions.³⁴

Rho-family GTPases are also important mediators of MV production.³⁵ Activation of RhoA is particularly effective for promoting the formation of MVs. The activation of RhoA has been shown to upregulate the downstream gene ARF6³⁶ or ARF1.³⁷ Thus, RhoA can indirectly accelerate the activation of MLCK, leading to the release of MVs into the extracellular space.³⁶ RhoA can also activate Rho-associated coiled-coil-containing kinases and LIM kinase, which promotes actin–myosin-based contraction for MV formation.^35,36 In general, inhibition of ARF6 or its targets reduces the release of MVs.²⁵

Characterization and Cargo of MVs

MVs can carry various proteins, some of which are present on their surfaces.³⁸ Therefore, MVs can be identified by certain markers: CD40, MMPs, ARF6, and extracellular matrix metalloproteinase inducer (EMMPRIN).^7,8,39,40 The cargos of MVs include membrane protein enzymes, growth factor receptors, cytokines, chemokines,⁴¹ lipids, and nucleic acids, including miRNAs, genomic DNA, and oncogenic genes.^11,42 (Table 1). Lo Cicero et al⁴³ demonstrated that Hsc70 was specifically concentrated on MVs, and MVs even contained Hsc70 constitutive partners at low levels. Bioactive molecules such as proteins, RNAs, and miRNAs are involved in tumor invasion and metastasis, and can change the function and phenotype of the receptor cells.⁴⁴ EMMPRIN (also termed CD147), a transmembrane glycoprotein present on the surface of tumor cells,⁴⁰ stimulates surrounding fibroblasts or tumor cells to produce MMPs.⁴⁵ These MMPs can decompose the basement membrane, and facilitate the proliferation, invasion, and metastasis of malignant tumor cells.⁴⁶ Menck et al⁴ showed that EMMPRIN could be used as a marker of MVs. EMMPRIN in a highly glycosylated form could activate the P38/mitogen-activated protein kinase (MAPK) signaling pathway of tumor cells and directly facilitate their invasion and metastasis.

Table 1.

Biomarkers of MVs

Biomarker Class	Name	MV Origin	Function	Target of Cargo	Ref.
Membrane-associated molecules	ARF6	Tumors	Remodeling of actin, regulation of MV shedding	VAMP3, MHC I, β 1-integrin	[25,28,29]
	β 1-integrin	Tumors	Cell adhesion	NA	[166]
	CD41	Plasma of CRC patients	Platelet aggregation and adhesion	NA	[167]
	Tissue factor (TF)	Activated platelets	Thrombus formation, activation of cancer stem cells, angiogenesis	NA	[168,169]
	EGFR EGFRvIII	Tumors Tumors (glioma)	Signal transduction, oncogenic growth factor receptor, activation of transforming signaling pathways (AKT and ERK)	NA NA	[60] [57]
	VAMP3	Tumors	Promotion of matrix invasion by tumor cells	MT1-MMP	[28,170]
	V-SNARE	Tumors	Interaction with Rab22a, mediation of additional cargo trafficking that converges on vesicle blebbing and shedding	Rab22a	[28]
	P-gp	Tumors (ALL)	Promotion of chemotherapeutic resistance	NA	[102]
	Ezrin	Tumors (leukemic and BC)	Co-localizes with P-gp and assists interaction of plasma membrane with cytoskeleton	NA	[96,171]
	PS	All cells	Membrane phospholipids	NA	[172]
	SM	All cells	Membrane phospholipids	NA	[53]
	CCL5, CCR6	Tumors (BC)	Metastasis, proliferation	NA	[173]
	CCR6	Tumors (GC)	Cancer cell-induced angiogenesis, promotion of cancer cell growth	NA	[173,174]
	CCR6, CX3CR1, CCL2	Tumors (CRC)	AKT kinase activation, antiapoptotic effects on monocytes	NA	[52]
	CCL2	Tumors (OC)	Improving survival rate	Doxorubicin	[175]
Intracellular components	MMP2	Tumors (BC, OC)	Degradation of extracellular matrix	NA	[176]
	MMP9	Tumors (BC, OC)	Degradation of extracellular matrix	NA	[176]
	uPA	Tumors (BC, OC, PC)	Degradation of extracellular matrix, promotion of tumor invasion	NA	[84,176]
	EMMPRIN (CD147)	Tumors (OC)	Production of extracellular matrix metalloproteinases, induction of proangiogenic, proliferation, and invasion activities	NA	[45,177]
	VEGF	Tumors (BC)	Proangiogenic factor	NA	[178]
	IL-1 β	Glial cells	Inflammation cytokine	NA	[179]
	TGF-β	Tumors (AML)	Decreasing cytotoxicity of NK cells	NKG2D	[180]
	tTG	Tumors (BC, glioblastoma)	Cross-linking with FN, induction of recipient fibroblast transformation	FN	[94]
Nucleic acids	miR-19b	Tumors (RC)	Promotion of invasion and metastasis	NA	[90]
	miR-29c	Tumors (RC)	Promotion of invasion and metastasis	NA	[90]
	miR-151	Tumors (RC)	Promotion of invasion and metastasis	NA	[90]
	miR-145	Tumors (CRC)	Drug resistance	NA	[106]
	miR-34a	Tumors (CRC)	Drug resistance	NA	[106]
	miR-1246	Tumors (CRC)	Promotion of angiogenic activities	NA	[181]
	miR-92a	Tumors (CRC)	Tumor angiogenesis, cell proliferation	Down-regulated DKK-3	[181,182]
	Let-7 miRNA family	Tumors (GC)	Oncogenesis, metastasis	NA	[183]
	miR-1289	Tumors (GBM)	Enhancement of MV enrichment	Zipcode-like 25-nt sequence, GALR3, MK/MDK	[184]
	miR-21	Tumors (lung and pancreatic cancer)	Induction of myoblast apoptosis	TLR7	[185]
	miR-143BPs	THP1 monocytes/macrophages	RNA drug delivery system	NA	[186]
	miR-150	Tumors	Promotion of tumorigenesis	Upregulation of VEGF	[187]
	miR-23a	Hypoxic tumors	Decrease of NK cells’ anti-tumor response	CD107a (LAMP1)	[188]
	miR-1227	Tumors (PC)	Promotion of migration	NA	[174]
	cDNA	Tumors	Leads to mutations, deletions, rearrangements, and changes in gene expression	NA	[151]
	gDNA	Tumors	Role in genetic communication between cells	NA	[151]
	ssDNA	Tumors	Role in genetic communication between cells	NA	[151]
	c-Myc	Tumors	Oncogene	NA	[151]
	pDNA	Tumors	Transfer of reporter function to recipient cells	NA	[189]

Abbreviations: MVs, microvesicles; ARF6, ADP-ribosylation factors 6; MHC I, major histocompatibility complex class I; VAMP3, vesicle-associated membrane protein 3; CD41, cluster of differentiation 41; CRC, colorectal cancer; TF, tissue factor; EGFR, epithelium growth factor receptor; MT1-MMP, membrane-type 1 matrix metalloprotease; v-SNARE, vesicular soluble N-ethylmaleimide-sensitive factor attachment protein receptor; P-gp, P-glycoprotein; ALL, acute lymphoblastic leukemia; PS, phosphatidylserine; SM, Sphingomyelin; CCL5, CC chemokine ligand 5; CCR6, CC chemokine receptor 6; BC, breast cancer; GC, gastric cancer; CRAC, colorectal adenocarcinoma; CCL2, CC chemokine ligand 2; OC, ovarian cancer; MMP2, matrix metalloproteinases 2; MMP9, matrix metalloproteinases 9; uPA, urokinase plasminogen activator; PC, prostate cancer; EMMPRIN, extracellular matrix metalloproteinase inducer; VEGF, vascular epithelium growth factor; IL-1β, interleukin-1β; TGF-β, transforming growth factor-β; AML, acute myeloid leukemia; tTG, tissue-type transglutaminase; GBM, human primary glioblastoma multiforme; FN, fibronectin; DKK-3, dickkopf-3; GALR3, galanin receptor 3; MK/MDK, midkine; TLR7, toll-like 7 receptor; NK cells, natural killer cells; LAMP1, lysosomal-associated membrane protein 1; gDNA, genomic DNA; pDNA, plasmid DNA; ssDNA, single-stranded DNA; NA, not acquired.

Methods for MVs Isolation and Detection

Isolation of MVs

Two methods have been developed for the isolation of MVs: traditional centrifugation and magnetophoretic sorting or immunoaffinity chromatography. The former approach is based on the physical properties of MVs and relies mainly on centrifugation and flotation in sucrose gradients, occasionally combined with size-exclusion chromatography.¹¹ It is well accepted that the centrifugation should be performed at 10,000–20,000 g for 30–60 min.⁴⁷ As the size distribution of MVs overlaps with that of other extracellular vesicles, isolation by centrifugation may lead to low purity of MVs. Cell sedimentation also depends on the density and cargo of vesicles.^47,48 Therefore, some researchers have proposed combining differential centrifugation with sucrose gradient ultracentrifugation to remove exosomes, or carrying out immune separation. The latter approach is based on MVs’ biochemical features and uses magnetophoretic sorting or immunoaffinity chromatography to isolate MVs.¹¹

Detection of MVs

Once MVs have been isolated, they require further characterization. ELISA and fluorescent-activated cell sorting are frequently used methods for quantifying MVs.^21,49 ELISA can capture a specific protein and produce a color change that is related to the concentration of the target protein. Annexin V is a commonly used marker for MV quantification by ELISA.²¹ Fluorescent-activated cell sorting can be used to detect MVs via conjugation with specific fluorescent antibodies.^49,50 In addition, electron microscopy provides direct evidence for the presence of MV structures and is more popular in the detection of MVs.⁴⁸

Tumor-Derived Microvesicles

TMVs can be separated from a patient’s biological fluids, such as peripheral blood, urine, saliva, and ascitic fluid.⁵¹ TMVs contain many surface determinants, including CD44H, major histocompatibility complex I (MHC I), EMMPRIN, chemokine receptors (CCR6, CX3CR1), and epithelial cell adhesion molecules. TMVs also contain growth factors including vascular endothelial growth factor (VEGF) and hepatocyte growth factor.⁵² These substances can promote tumor cell proliferation and adhesion and decomposition of the ECM to facilitate tumor metastasis. Several in vivo and in vitro experiments have confirmed that the amount of MV secretion is linked to tumor aggressiveness. Kim et al⁵³ demonstrated that sphingomyelin is the active component in MVs that induces endothelial cell migration, tube formation, and angiogenesis.

TMVs and the TME

The occurrence and development of cancer strongly depend on the surrounding microenvironment, which contains both cellular and non-cellular components.⁵⁴ TMVs have important roles in the TME because they can efficiently transfer bioactive contents.^11,15 TMVs can also regulate the immune response in the TME and are important mediators of tumor progression.^55,56 Muralidharan Chari et al⁴⁴ showed that TMVs released from invasive prostate cancer PC3 cells promoted the phosphorylation of ERK and upregulated MMP9, thereby increasing the apoptosis resistance of fibroblasts. In turn, the activated fibroblast-derived MVs promoted the invasion and metastasis of PC3 cells. This feedback phenomenon indicated that prostate-cancer-derived MVs activated stromal cells in the TME.

It is widely accepted that epidermal growth factor receptor variant III (EGFRvIII) is a truncated and oncogenic form of the epidermal growth factor receptor. Al-Nedaw et al⁵⁷ found that TMVs from aggressive glioma containing EGFRvIII merged with the plasma membrane of indolent glioma cells, resulting in induced activation of MAPK and Akt, increased expression of EGFRvIII-regulated genes (VEGF, Bcl-x(L), p27), morphological transformation, and an increase in anchorage-independent growth. Overall, the TMVs caused a transfer of oncogenic activity.⁵⁷ Tumor growth requires a continuous blood supply to satisfy the demand for nutrition and metabolism through angiogenesis.⁵⁸ TMVs also contain regulators of angiogenesis such as VEGF, bFGF, and EGFR.^59–61 Al-Nedaw et al⁶⁰ reported that TMVs stimulated stromal fibroblasts to secrete angiogenic precursors and delivered the activated EGFR from A431, A549, and DLD-1 cells to surrounding fibroblasts. Notably, VEGF expression in endothelial cells and autocrine activation of VEGF receptor-2 were attributed to intercellular transfer of EGFR.

VEGF, which is released from tumor cells, is a potent factor that promotes tumor angiogenesis.⁶² MV-containing tissue factor (TF) has been reported to induce the secretion of VEGF and stimulate angiogenesis.⁶³ Szubert et al⁶¹ showed that TMVs could carry EMMPRIN (CD147) and promote the secretion of VEGF, thereby inducing angiogenesis of ovarian cancer.⁶¹ By contrast, Zhang et al⁵⁹ found that TMV-delivered miR-29a/c suppressed vascular cell growth via inhibition of VEGF expression in gastric cancer cells. Therefore, they speculated that miRNA-containing MVs could be developed to inhibit tumor growth by blocking angiogenesis, a novel anti-tumor strategy. TMVs have also been shown to support thrombosis. It is well known that cancer cells can express TF and deliver TF-positive TMVs to the circulation. Geddings et al⁶⁴ observed that TF-positive TMVs induced platelet activation, contributing to thrombosis in cancer patients. TF-positive TMVs could also destroy the function and structure of normal tissues and organs.

TMVs and Immunosuppression

Tumor cells can induce immunosuppression via TMVs so that abnormally proliferating tumor cells are not recognized and attacked by the immune system. TMVs participate in immunosuppression in two ways. TMVs regulate the proliferation and differentiation of various types of immune cells by delivering specific ligands for binding to immune cells. Tumor-associated macrophages, which are among the important immune cells in the TME, can be divided into the M1 population (pro-inflammation) and M2 population (anti-inflammation). Thus, M2-polarized macrophages can inhibit the anti-tumor immune response mediated by T cells and promote metastasis.^65,66 Ma et al⁶⁷ demonstrated that the development of M2-type macrophages via TMVs was mediated by the cGAS/STING/TBK1/STAT6 pathway, with subsequent anti-inflammation and immunosuppressive effects. IL-1β is an important proinflammatory cytokine.^68,69 In the TME, IL-1β is involved in the malignant behavior of tumor cells.⁷⁰ Chen et al⁷¹ found that lung cancer microparticles (L-MPs) could induce macrophages to release IL-1β, which in turn promoted the development of the immunosuppressive TME. The underlying mechanism was related to the activation of Toll-like receptor 3 and the Nod-like receptor protein 3 inflammasome via L-MPs.

TMVs have been reported to have a positive effect on the immunogenicity of dendritic cells (DCs) via reprogramming their antigen-processing mechanism and intracellular signaling transduction pathway, thereby promoting the anti-tumor response.⁷² Valenti et al⁷³ reported that TMVs promoted the generation of myeloid-derived suppressive cells (MDSCs) via impairing the differentiation of monocytes to DCs. MDSCs further exert inhibitory effects on T cell proliferation and function through the secretion of transforming growth factor-beta (TGF-β).^8,56 TMVs have immunoregulation ability and have effects on multiple aspects of regulatory T cells (Tregs), including induction, promotion of expansion, upregulation of the suppressor function, and reinforcement of resistance to apoptosis. It is also possible for TMVs to present TGF-β to CD4⁺ Tregs to promote immunosuppression.⁷⁴ TMVs inhibited IL-2 to weaken the anti-tumor response of natural killer cells (NK cells) and CD8⁺ T cells. Conversely, TMVs enhanced the immunosuppressive ability of CD4⁺/CD25⁺/Foxp3⁺ Tregs via TGF-β.⁷⁴ In addition, Taylor et al⁷⁵ showed that TMVs could promote T cell apoptosis through Fas ligand (FasL; CD95L).

FasL is a transmembrane protein that is a member of the tumor necrosis factor (TNF) superfamily and regulates apoptosis in the immune system.⁷⁶ It has been reported that activated T cells with co-expression of Fas and FasL leads to activation-induced cell death.⁷⁷ TMVs promote apoptosis through binding of FasL to the corresponding receptors on CD4⁺ T cells. Kim et al⁷⁸ proved that the level of FasL-related MVs was related to tumor burden and lymph node involvement. TMVs could help cancer cells’ evasion of the immune response. Reports have shown that TMVs could induce apoptosis in activated CD8⁺ T cells by exposing FasL and TNF-related apoptosis-inducing ligands.^79–81 Cancer-cell-derived MVs contain miRNAs that regulate various immune components, including cytotoxic T lymphocytes, NK cells, MDSCs and Tregs to shape immune microenvironment.⁸² For example, Cui et al⁸³ reported that leukemia-derived MVs induced T cell exhaustion through delivery of multiple exogenous miRNAs into T cells by interfering in the NF-κB pathway.

TMVs and Invasion

Tumor invasion depends on the degradation of the ECM, which is mainly caused by proteases including MMP-2, MMP-9, and urokinase-type plasminogen activator (uPA). These proteases can degrade basement membrane collagen and various components of the ECM including fibrin.^23,47 TMVs have been shown to contain these proteases. Angelucci et al⁸⁴ reported MVs derived from aggressive prostatic carcinoma cells released uPA, which adheres to and degrades collagen IV, and reconstructed the basement membrane. Graves et al⁸⁵ found that MVs from ovarian cancer and malignant ascites contained activated MMP-2, MMP-9, and uPA, which resulted in ECM degradation and tumor invasion. In contrast, inhibition of MMP-2 and MMP-9 reduced tumor invasion.⁸⁶

TMVs and Tumor Metastasis-Related Phenotypes

Tumor metastasis is one of the leading causes of death and the predominant challenge in the treatment of cancer patients.⁸⁷ Metastasis is a process of multiple cascades, starting with the loss of adhesion of cancer cells at the primary tumor site. These cells then invade the surrounding tissue and enter the blood circulation. After evading the cytotoxicity of the host immune system, the cells extravasate and colonize a distant site for secondary growth. TMVs have been shown to be involved in this process.⁸⁸ Al-Nedaw et al⁵⁷ demonstrated that TMVs could promote the horizontal transmission of oncogenes and transformation phenotypes among subpopulations of tumor cells. In addition, an EGFRvIII kinase inhibitor significantly reduced the signal responses of receptor cells mediated by TMVs, indicating a correlation between EGFRvIII carried by TMVs and the cascade reaction of receptor cells.

Lung cancer and breast cancer cells can absorb platelet-derived MVs and obtain platelet-related adhesion molecules, which are beneficial to tumor cell adhesion and metastasis.⁸⁹ Skog et al⁴¹ found that brain microvascular epithelial cells could absorb MVs containing mRNAs and miRNAs secreted by malignant glioma cells. It was speculated that tumor cells could change the phenotype of stromal cells via miRNAs; this change was conducive to the survival and expansion of tumors. Tumor cells interfere with the gene stability of surrounding or distant cells via TMVs and destroy the structure and function of normal tissues and organs.

Given their high expression of the c-Myc oncogenic gene, TMVs may be involved in reverse transcription. Abnormal initiation of retrotransposon and insertion of complementary DNA may mediate gene mutation, rearrangement, and deletion.⁹⁰ Grange et al⁹⁰ reported that lung metastasis of renal carcinoma was promoted by MVs from CD105⁺ cancer stem cells. The molecular characterization of CD105⁺ MVs was used to identify a group of angiogenic mRNAs and miRNAs, including miR-19b, miR-29c, and miR-151, which were related to tumor progression and metastasis. Finally, cancer stem cell-derived MVs were identified; these could trigger angiogenesis switching and coordinate metastasis during tumor progression.

Zhang et al⁹¹ demonstrated that circulating TMVs could easily enter the lung parenchyma, where they were absorbed by local macrophages and induced the production of CC chemokine ligand 2 (CCL2). CD11b⁺ Ly6C⁻ macrophages were attacked by CCL2, matured into an F4/80⁺ phenotype producing IL-6, and triggered fibrin deposition. Therefore, circulating TMVs favor cancer metastasis to the lung, because IL-6 and fibrin deposition can provide chemical and mechanical signals that promote the survival and growth of lung cancer regenerative cells. The lipid receptor CD36 is the major mediator of the engulfing of pancreatic tumor-derived MVs by myeloid immune cells. Pancreatic tumor-derived MVs also promoted metastasis, which was related to CD36-regulated immune cell invasion and extravasation of MVs.⁹² Moreover, stimulation with TNF-ɑ markedly increased the ability of TMVs to induce immigration of tumor cells.⁹³

It is well accepted that epithelial-mesenchymal transition (EMT) has a crucial role in tumor metastasis. Recent studies have shown that TMVs also regulate EMT. Antonyak et al⁹⁴ found that MVs released by breast cancer or glioma cells could mediate the transfer of crosslinking fibronectin and tissue transglutaminase to recipient cells, activating mitotic signal activity and endowing normal fibroblasts and epithelial cells with characteristics of cancer cells, such as anchorage-independent growth and enhancing survival capability. In addition, Castellana et al⁹⁵ found that TMVs could induce fibroblast activation via phosphorylation of ERK1/2 and upregulation of MMP-9. The activated fibroblasts also promoted the release of MVs and reprogrammed them into CAFs. CAF-derived MVs may participate in the process by which CAFs induce EMT or stemness in cancer cells by releasing certain soluble factors.⁷

TMVs and Drug Resistance

Drug resistance refers to the ability of cancer cells to survive the effects of anti-tumor drugs. Anti-tumor treatment often fails owing to multidrug resistance (MDR), which is mainly mediated by a plasma membrane multidrug efflux transporter, P-glycoprotein (P-gp).²⁴ MDR enables tumor cells to evade the cytotoxic effects of chemotherapeutic drugs through the active efflux of intracellular drugs.⁹⁶ Experimental and clinical patient studies have indicated that TMVs are associated with drug resistance in various types of cancer, including breast cancer, ovarian cancer, colorectal cancer, and acute lymphoblastic leukemia (ALL).⁹⁷ In addition, TMVs can be used to monitor disease burden, progression, and MDR development in myeloma.⁹⁸ It has been reported that P-gp-mediated MDR can be acquired via TMVs, in a novel “non-genetic” acquisition process involving intercellular transfer. This finding indicates that TMVs represent an important medium for the transmission of MDR and suggests a new type of strategy to prevent MDR.⁹⁹

In breast cancer, a protein carried by TMVs has been reported to promote drug resistance. For example, the transient receptor potential channel 5 (TRPC5) has been shown to regulate P-gp expression.¹⁰⁰ TMVs transferred TRPC5 to human mammary epithelial cells (HMECs) and induced P-gp expression by activating nuclear factor of activated T cells subtype C3. Consistent with these results, a TRPC5-blocking antibody, T5E3, downregulated MDR1 expression and reduce P-gp production in HMECs.¹⁰¹ Circulating TMVs containing TRPC5 may transfer drug resistance to non-drug-resistant cells. Namee et al⁹⁷ found that over-expression of ubiquitin C-terminal hydrolase L1, a deubiquitinating enzyme, induced MDR in breast cancer via upregulation of P-gp through the MAPK/ERK pathway. Bebawy et al¹⁰² co-cultured MVs of drug-resistant tumor cells with drug-sensitive tumor cells; the results suggested that the TMVs could bind to the drug-sensitive tumor cells and express P-gp, driving resistance to anthracycline. TMVs released by vinblastine-resistant leukemic cells, which overexpressed the MDR1/P-gp gene, conferred resistance on the sensitive ALL cell line CCFR-CEM by the transfer of P-gp protein.

Drug resistance has been shown to be related to a reduction in the accumulation of P-gp substrate rhodamine 123 or doxorubicin.¹⁰² Some evidence also suggests that TMVs carrying P-gp are involved in the spread of drug resistance in ovarian cancer.¹⁰³ miRNAs mediate therapeutic resistance through inducing EMT and stemness.¹⁰⁴ A study by Klumper¹⁰⁵ suggested that miR-142-5p expression in both peripheral blood and bone marrow samples could predict the response of treatment-naïve chronic myeloid leukemia to imatinib. Akao et al¹⁰⁶ established 5-fluorouracil (5-FU)-resistant human colon cancer DLD-1 cells (DLD-1/5-FU cells) from 5-FU-sensitive DLD-1 cells. Their results showed that intracellular and extracellular miR-145 and miR-34a were closely related to 5-FU resistance, and that the resistance was partly due to increased secretion of miR-145 and miR-34a by TMVs, resulting in lower intracellular levels of the two miRNAs.

MVs and Intercellular Communication

MVs are important mediators of intercellular communication. They perform this function in the following ways: 1) they deliver proteins, bioactive molecules, and mRNAs to target cells; 2) they fuse with target cells to transfer surface receptors from them, and perform biofunctions via binding between receptors and ligands; and 3) they stimulate target cells via surface ligands, functioning as a signaling complex.¹⁰⁷ For example, Melzani et al¹⁰⁸ found that MVs shed from melanoma can express FasL on their surface, enabling them to induce apoptosis by binding to CD95 on T-lymphocytes. This may be a mechanism by which cancer cells escape from tumor-infiltrating lymphocytes. There is also evidence that TMVs increase the survival of tumor-infiltrating lymphocytes. TMVs undergo changes in their immunophenotype and biological activity through communication with these cells.

Baj-Krzyworzeka et al⁵² found that MVs derived from human cancer cell lines transferred many tumor determinants (such as CCR6/CD44v7/8) to monocytes; these could protect monocytes from apoptosis by activating AKT kinase–phosphatidylinositide 3′-OH kinase. This suggested that TMVs might function as mediators of communication between monocytes and tumor cells. Samii et al¹⁰⁹ proposed that miRNA-containing MVs could directly affect the phenotypic and functional characteristics of target cells. For example, miR-21 was reported to be overexpressed on cells of hematological malignancies such as leukemia, lymphoma, and multiple myeloma.^110–112 Transfer of miR-21 by leukemia MVs to hematopoietic stem and progenitor cells (HSPCs) led to their overexpression, which induced HSPCs proliferation. It was shown that miR-29a regulated early hematopoiesis by inducing self-renewal capacity of myeloid progenitors and promoting their conversion into leukemia stem cells. Upregulation of an oncogenic miRNA (miR-29a) in MVs resulted in the transformation of normal HSPCs into leukemia-like cells.^109,113

An increasing number of miRNAs have been shown to mediate proliferation, EMT, and cancer stemness through diverse targets.¹⁰⁴ For example, Le et al¹¹⁴ demonstrated that MVs derived from murine and human breast cancer cells could be used to deliver miR-200 to nonmetastatic cancer cells, promoting mesenchymal-to-epithelial transition. Tumors expressing miR-200 and MVs from murine cancer and human xenograft models facilitated metastasis of poorly metastatic cells at both nearby and distant sites, and endowed these cells with the ability to colonize distant tissues in a miR-200-dependent manner. Finally, the results clarified that metastatic ability could be transferred via the uptake of MVs.

MVs and Other EVs

Differences Between MVs and Other EVs

As mentioned above, EVs include MVs, exosomes, oncosomes, and apoptotic bodies. EVs are commonly identified by their cellular origin, size, density, markers, molecular cargos, and so on¹¹⁵ (Table 2).

Table 2.

Distinctions Among Microvesicles, Exosomes, Oncosomes, and Apoptotic Bodies (Classification of Extracellular Vesicles)

Vesicle Type	Microvesicles	Exosomes	Oncosomes	Apoptotic Bodies
Origin	Plasma membrane	Multivesicular bodies (MVBs)	Plasma membrane	Plasma membrane
Biogenesis	Shedding from the plasma membrane	Fusion of endosomes with the plasma membrane (exocytosis of MVBs)	Shedding from aggressive cancer cells	Outward blebbing of apoptotic cell membrane
Size (nm)	100–1000	40–160	100–4000 (large oncosomes, 1000–10,000)	50–5000
Markers	CD40, ARF6, EMMPRIN, integrin, selectin	Tetraspanins, ALIX, CD9, CD63, CD81, HSP, ESCRT, TSG101, flotillin	Cav-1, CK18, HSP70, HSP90	Large amounts of phosphatidylserine, annexin V, DNA, histones
Contents	mRNA, non-coding RNAs, cytoplasmic and membrane proteins, including receptors	mRNA, non-coding RNAs, cytoplasmic and membrane proteins, including receptors and major histocompatibility complex molecules	Oncogenic proteins, mRNAs, and non-coding RNAs	Nuclear fractions, cell organelles
Major pathway	Ca2+-dependent	ESCRT– dependent	AKT1 and EGFR pathways	Apoptosis-related pathway
Detection methods	EM, FACS	EM, FACS with CD68 capture and Western blotting	EM, confocal, or optical microscopy	EM, FACS
Isolation methods	Centrifugation (10,000–20,000 g) magnetophoretic sorting or immunoaffinity chromatography	Ultracentrifugation (≥100,000 g), immunoprecipitation (ExoQuick), SEC	No standard method	No standard method
References	[1,4,7,8,21,23,24,41,47–50]	[1,3,7,118,120,123]	[7,123,124,190]	[7,122,123]

Abbreviations: CD9, cluster of differentiation 9; CD63, cluster of differentiation 63; CD81, cluster of differentiation 81; EM, electron microscopy; EMMPRIN, extracellular matrix metalloproteinase inducer; ESCRT, endosomal sorting complex required for transport; FACS, fluorescence-activated cell sorting; HSP, heat shock protein; SEC, size exclusion chromatography; PS, phosphatidylserine.

Exosomes, which range from 40 to 160 nm in diameter,³ originate from invagination of the endosomal limiting membrane and form as intraluminal vesicles (ILVs), resulting in the generation of multivesicular bodies (MVBs). When an MVB has been generated, it can fuse with the plasma membrane to release ILVs, which are referred to as exosomes.¹¹⁶ The classical mechanism of the biogenesis of exosomes relies on the endosomal sorting complex required for transport (ESCRT). The ESCRT is a protein complex that is essential for the scission of ILVs into the MVB lumen.^1,117 It is well accepted that exosomes can be distinguished via their markers, for example, ALIX, CD9, CD63, CD81, and heat shock protein.³ The cargos of exosomes include mRNAs and non-coding RNAs, and cytoplasmic and membrane proteins such as receptors and major histocompatibility complex molecules.^7,118,119 The methods used to isolate exosomes include ultracentrifugation, density gradient centrifugation, immunoprecipitation, and size-exclusion chromatography.¹²⁰ Electron microscopy, fluorescent-activated cell sorting with CD68 capture, and Western blotting are used for the detection of exosomes.⁷ Exosomes are important carriers in signal transduction among different types of cells in the TME. Multiple studies have confirmed the role of exosomes in the development and progression of hepatocellular carcinoma (HCC).¹²¹

Oncosomes, like MVs, are derived from the plasma membrane, which is shed from aggressive cancer cells. There are two types of oncosomes, including oncosomes (100–4000 nm in diameter) and large oncosomes (LOs, 1–10 μm in diameter).¹²² Minciacchi et al⁷ found that the formation of LOs relied on the activation of the AKT1 and EGFR pathways. The markers of oncosomes include caveolin-1,¹²³ and their cargos of oncosomes include oncogenic proteins, mRNAs, and non-coding RNAs.¹²⁴ There are currently no standardized methods for the isolation of oncosomes; however, they are commonly identified by electron microscopy and confocal or optical microscopy.¹²⁴

Apoptotic bodies are outward blebbings of the apoptotic cell membrane, with diameters of 50–2000 nm.¹²² Apoptotic bodies contain nuclear fractions and cell organs. They can be identified by hallmarks including annexin V, DNA, and histones.¹²³ Similar to the case of oncosomes, there are no standardized methods for isolation of apoptotic bodies.⁷ They are usually observed by electron microscopy.

Cross-Talk Between MVs and Other EVs

JAK-STAT signaling mediates many immune regulatory processes, including recognition of tumor cells and immune escape.¹²⁵ Interferon-γ (IFN-γ)-induced STAT1 activation is related to the anti-tumor immune response; STAT1 is generally regarded as a inhibitor of tumor activity. Conversely, STAT3 is mainly associated with cancer cell survival, immunosuppression, and inflammation in the TME.¹²⁶ Bourdonnay et al¹²⁷ reported that alveolar macrophage-derived MVs could secrete SOCS3, whereas exosomes secreted SOCS1; these proteins were absorbed via alveolar epithelial cells (AECs) and inhibited STAT activation. Moreover, SOCS3-containing MVs absorbed via AECs could suppress IL-6, leading to STAT3 activation. However, SOCS1-containing exosomes taken up by AECs could inhibit IFN-γ-induced STAT1 activation.

EGFR signaling mediated by EVs influenced tumor progress and metastasis. TMVs transferred oncogenic EGFR to other cancer or epithelial cells, increasing the growth and survival of glioma cells,⁵⁷ and led to angiogenesis in human squamous cell carcinoma.⁶⁰ Moreover, gastric cancer-derived exosomes also contained the oncoprotein EGFR, which eventually localized to the plasma membranes of liver stromal cells. Exosome-mediated EGFR activated liver hepatocyte growth factor, bound to c-Met on tumor cells, and promoted the seeding and proliferation of cancer cells in metastasis.¹²⁸ Amphiregulin is an EGFR ligand that facilitates the invasive ability of cancer cells. Higginbotham et al¹²⁹ illustrated this phenomenon in breast and colon cancer-derived exosomes. Subsequently, they found that the exosomes expressed EGFR and amphiregulin in colon cancer.¹³⁰ Tumor-derived EVs have procoagulant properties that might cause tumor-associated thrombosis, which is related to metastasis. Gomes et al¹³¹ found that EVs (including MVs and exosomes) released by MA-MB-231 cells were enriched in TF, which induced the generation of thrombin and subsequent plasma clotting and platelet aggregation (Figure 2).

Figure 2.

The cross-talk between MVs and exosomes. MVs and exosomes are released from many cells, including tumor cells, CAFs, and TAMs. They can secret MVs-containing EGFR and exosomes-containing EGFR, which influence tumor progression, for example, transforming normal cells into tumor cells, promoting angiogenesis and metastasis. Moreover, normal cells, which take up MVs and exosomes can increase the growth and survival of tumor cells by activating the MAPK/AKT pathway.

Abbreviations: CAFs, cancer-associated fibroblasts; TAMs, tumor-associated macrophages; EGFR, epidermal growth factor receptor.

Clinical Applications of TMVs

Cancer Vaccines

The basic principle of tumor vaccines is to enhance the anti-tumor immunity of T cells using the characteristics of tumor antigens presented by MVs. TMVs are potential carriers for antigen delivery because they can carry many immunogenic molecules, for instance, proteins, nucleic acids, and polysaccharides. Moreover, TMVs can directly target cancer cells.¹⁶ EV vaccines were first used to prevent infectious diseases, including diphtheria, Mycobacterium tuberculosis, and Bordetella pertussis.^132–134 Subsequently, investigators found that EV vaccines could be adapted for tumor therapy.¹³⁵ MVs released by macrophages infected with Listeria monocytogenes were shown to transfer Listeria monocytogenes antigens to DCs, thereby inducing protective T cell immunity.¹³⁶ Dong et al¹³⁷ suggested that an oral anti-tumor TMV-based vaccine could be absorbed by ileal epithelial cells (IECs). On the one hand, the TMVs could activate nucleotide-binding oligomerization domain 2 and downstream MAPK and NF-κB, causing IECs to release chemokines to recruit CD103⁺ CD11c⁺ DCs. On the other hand, they could be transported by IECs to the basolateral part, where DCs could capture the contents of TMVs cross-presenting antigen. Thus, TMVs could transfer antigens or innate signals (such as DNA) to intestinal mucosal DCs.

Tumor cells containing DNA and TMVs were exposed to ultraviolet light to induce release of antigen fragments. After being absorbed by DCs, the TMVs’ DNA induced the expression of IFN-I by activating the cGAS/STING pathway. In turn, IFN-I enhanced the maturation of DCs by upregulating CD80, CD86, and MHCII. Then, the “armed” DCs activated tumor-specific T cells, resulting in the lysis of tumor cells. Zhang et al^138–140 proposed TMVs as ideal candidates for use in developing novel and effective tumor vaccines. Pineda et al¹⁴¹ used non-irradiated and irradiated TMVs derived from C6 glioma cells to immunize rats with glioma. Compared with the control group (immunized with non-irradiated TMVs), the group treated with irradiated TMVs (IR-TMVs) showed increased release of TMVs with the specific antigen. The IR-TMVs were also conducive to the expansion of effector T cells, enabling them to migrate into tumors and promote the death of tumor cells via immunogenicity. Therefore, the authors speculated that IR-TMVs could be used as therapeutic anti-tumor vaccines.

Parenky et al¹⁴² prepared an oral tumor vaccine using TMVs extracted from mouse prostate cancer cells and evaluated its anti-tumor effects in vivo combined with cyclophosphamide and granulocyte-macrophage colony-stimulating factor. The tumor vaccine based on the TMVs in combination with two drugs significantly reduced Tregs in vivo, indicating that the vaccine would have a strong anti-tumor effect. Pack et al¹⁴³ combined TMVs derived from 4T1 tumor cells with immunostimulatory molecule B7-1 (CD80), anchored by glycosylphosphatidylinositol (GPI) and IL-12 molecules, to make a vaccine; then, tumor-bearing mice were treated with the TMV vaccine alone or in combination with an anti-cytotoxic T-lymphocyte-associated protein 4 monoclonal antibody. The combined therapy improved the survival rate of mice and reduced lung metastasis. In addition, it was verified that the vaccines exerted their effects through tumor-specific CD8⁺ T cell immunity.

TMV-mediated immunotherapy has been shown to be a potential enhancer of immunosuppressants for the treatment of metastatic triple-negative breast cancer. Bommireddy et al¹⁴⁴ found the same effects of TMV vaccines in a mouse model of head and neck squamous cell carcinoma (HNSCC). They also found that the TMV vaccines could effectively inhibit tumor growth in MOC1 and MOC2 murine oral cancer models and cooperate with anti-PD1 to prolong the survival time of tumor-bearing mice. Moreover, TMV vaccines could be used to develop immunotherapies for HNSCC and to enhance the efficacy of immune checkpoint inhibitors.

Biomarker

Owing to their stability, TMVs extracted from body fluids of cancer patients can provide diagnostic information.^41,145 Hou et al¹⁴⁶ found that pyruvate kinase M2 (PKM2) could be isolated from the plasma of patients with HCC, suggesting that PKM2 in TMVs could be used as a potential diagnostic marker of HCC. Muralidharan-Char et al²⁵ found that the activation of ARF was directly related to tumor progression and thus may represent a disease biomarker. A pilot study by Smalley et al¹⁴⁷ identified eight tumor-related proteins in TMVs, comprising five proteins related to the EGFR pathway, the ɑ-subunit of GsGTP-binding protein, resistin, and retinoic acid-induced protein 3. Thus, the protein composition of such TMVs could be used in the early detection of bladder cancer.

HER-2/neu is upregulated not only in breast cancer but also in other related carcinomas, for example, gastric cancer and ovarian cancer.^148,149 Baran et al¹⁵⁰ found higher expression levels of HER-2-/neu, MAGE-1, c-MET, and EMMPRIN in plasma samples of gastric cancer patients compared with control samples, suggesting that these proteins could be used as diagnostic markers. Zhong et al³⁸ proposed EMMPRIN as a novel potential tumor marker that could be used to evaluate the prognosis of patients with malignant tumors at an early stage and to adjust the treatment plan, thereby improving the quality of life of cancer patients. Balaj et al¹⁵¹ observed amplification of the oncogene c-Myc in TMVs, suggesting that TMVs contain genetic information that could be a source of potential cancer biomarkers. Sun et al¹⁵² isolated and characterized TMVs from saliva of patients with lung cancer and found that they contained informative proteins, including BPI fold-containing family A member 1 (which is involved in the innate immune response), MUC5B (which is involved in the pathogenesis of pulmonary fibrosis), and Ras GTPase-activating-like protein (which is involved in tumor cell proliferation and transformation); these markers could be used to detect lung cancer in a non-invasive manner. Elevated levels of saliva MVs (SMVs) are associated with unfavorable clinicopathological features and decreased survival rate in patients with oral squamous cell carcinoma (OSCC). A study by Zhong et al¹⁵³ suggested that SMVs from OSCC were potential biomarkers of malignant progression.

Other Clinical Applications

Stem-cell-like tumor repopulating cells (TRCs) play a vital part in reprogramming the tumor immunosuppressive microenvironment.¹⁵⁴ Ma et al¹⁵⁵ showed that TMVs loaded with anti-tumor drugs could reverse the drug resistance of TRCs or stem-cell-like cancer cells. In addition, TRCs had greater flexibility than differentiated cancer cells, and they preferentially absorbed TMVs with anticancer drugs, leading to the death of TRCs. Tang et al¹⁵⁶ packaged chemotherapeutic drugs into TMVs, which could be collected and used to effectively kill tumor cells in mouse models without typical side effects. Studies have shown that TMVs are well-tolerated in clinical practice, and they achieved objective clinical efficacy in patients with lung cancer. A variety of therapeutic drugs, including oncolytic adenovirus, chemotherapeutic drugs, nucleic acids, antibodies, and antigens, have been carried to the targeted area for corresponding tumor treatment.¹⁵⁷ Autologous tumor-cell-derived MVs packaged with chemotherapeutic agents have been approved as a new biologic therapy for the treatment of malignant tumors after proving to be safe and well-tolerated.¹⁵⁷

Ran et al¹⁷ found that TMVs were a good carrier system that could deliver oncolytic adenovirus to tumors and induced highly efficient cytolysis. This delivery of oncolytic adenovirus by TMVs had various advantages. First, it avoided the host to develop antiviral effects. Second, it was highly efficient, because the entry of the virus into tumor cells was not limited by the need for a virus-specific receptor. Finally, TMVs could deliver oncolytic adenovirus to the nucleus of tumor cells and stem-like TRCs. Saari et al¹⁵⁸ clarified that MVs derived from prostate cancer cells could be used as carriers of paclitaxel, delivering drugs to the recipient cells via endocytosis, with an increased cytotoxic effect. Krishnan et al¹⁵⁹ reported that the levels and phenotypes of CD138⁺/CD41a⁻ MVs originating from multiple myeloma could be used as indicators of disease state and therapeutic outcomes in multiple myeloma patients. Their study demonstrated that TMV could be used as a novel prognostic biomarker to monitor malignant cells. Chen et al¹⁶⁰ proposed a donor-cell-assisted membrane biotinylation strategy to achieve biocompatible quantum dot labeling of TMVs. By further encapsulation with small interfering RNAs, the TMVs were converted into intercellular mediators as functionalized carriers for combined bioimaging and tumor-targeted therapy. Their investigation may have changed the field with the analysis and application of TMVs and provided a novel idea for the preparation of nanocarriers (Figure 3).

Figure 3.

Applications of tumor-derived microvesicles (TMVs). TMVs are released by tumor cells in the tumor microenvironment (TME). TMVs can be used as a delivery system, for instance, carrying chemotherapeutic drugs (paclitaxel), oncolytic adenovirus, P-gp, or miR-145a to the target area for cancer treatment. TMVs carrying P-gp reverse the drug resistance of tumor cells. Owing to their stability, TMVs can provide diagnostic information when extracted from body fluids of cancer patients, including patients with lung cancer, hepatocarcinoma, gastric cancer, and ovarian cancer. Examples of markers include PKM2, resistin, EMMPRIN, and MAGE-1. TMVs can carry a variety of immunogenic molecules, including proteins, nucleic acids, and polysaccharides. TMVs can transfer antigens or innate signals (DNA or others) to dendritic cells (DC); then, the armed DCs activate tumor-specific T cells, resulting in the lysis of tumor cells.

Abbreviations: PKM2, pyruvate kinase M2; EMMPRIN, extracellular matrix metalloproteinase inducer.

Conclusion and Perspective

MVs are special extracellular vesicles that are widely present in various body fluids. Many factors increase the number of MVs shed from cells, including hypoxia, irradiation, chemotherapy, and cell activation.^34,154,161 MVs carry large amounts of biological information that can be acquired by non-invasive technology; thus, they have broad applications as clinical tumor biomarkers. Both normal cells and malignant tumor cells can produce MVs; however, the numbers and nature of the MVs are different, and the biomarkers are also distinct. The protein molecules contained in MVs may reflect the molecular properties of the tumor cells from which they originate; therefore, they can be used as prognostic factors for TNM stage and response to therapy.

Owing to their phospholipid bilayer structure, MVs can fuse with the target cell membrane and thus transport anti-tumor drugs into cells. Therefore, MVs with targeted properties may be good carriers for anti-tumor therapies. Local invasion and distant metastasis are important factors associated with poor prognosis in patients with malignancy. MVs can be used as carriers to carry biological signals or molecules that promote invasion and metastasis of tumor cells and can serve as biomarkers to predict the prognosis of cancer patients. Although MVs have broad application as biomarkers, there are still some challenges to be resolved. For example, the release of MVs may be affected by age, infection, and inflammation. In addition, the sensitivity of detection is a major obstacle in the development of tumor-specific markers.¹⁶² The diameters of exosomes range from 40 to 160 nm,¹²⁰ whereas MV have diameters ranging from 100 to 1000 nm; thus, exosomes overlap with MVs in terms of size. Therefore, studies should carefully distinguish between exosomes and MVs. So far, methods for isolation of MVs have been based on primary centrifugation, which collects the supernatant to abolish cell fragments. This is followed by separation of cell-free extracts using size-exclusion chromatography, filtration, precipitation, magnetophoretic sorting, and immunoaffinity chromatography. However, there is still a need for high-efficiency methods to be developed. In particular, the current methods for isolation of MVs pose obstacles to achieving clinical-grade quality.

MVs serve as mediators of intercellular communication by delivering components to target cells, thereby modifying phenotypes and reprogramming cell function. Therefore, it is worth exploring the effects of MV-mediated intercellular communication on tumor progression. Tumor vaccines related to exosomes, including ascitic cell-derived exosome vaccines and DC-derived exosome vaccines, have entered Phase I clinical trials and are expected to show excellent results.^163–165 However, there are no TMV vaccines currently moving to clinical trials.

Funding Statement

This work was supported by the National Natural Science Foundation of China (No. 81874120, No. 82073370).

Abbreviations

MVs, microvesicles; MMPs, matrix metalloproteinases; ARF6, ADP-ribosylation factor 6; TMVs, tumor-derived microvesicles; TME, the tumor microenvironment; CAFs, cancer-associated fibroblasts; ECM, extracellular matrix components; miRNAs, microRNAs; MLCK, myosin light-chain kinase; MLC, myosin II light chain; ERK, extracellular signal-regulated kinases; ELISA, Enzyme-linked immunosorbent assay; EGFRvIII, epidermal growth factor receptor variant III; EMT, epithelial-mesenchymal transition; EMMPRIN, extracellular matrix metalloproteinase inducer; APCs, antigen-presenting cells; FasL, Fas ligand; HSPCs, hematopoietic stem and progenitor cells; L-MPs, lung cancer microparticles; MAPK, mitogen-activated protein kinase; MHC I, major histocompatibility complex I; CCR6, CC chemokine receptor 6; VEGF, vascular endothelial growth factor; IL-8, interleukin-8; TNF, tumor necrosis factor; TF, tissue factor; ILVs, intraluminal vesicles; MVB, multivesicular body; ESCRT, endosomal-sorting complex required for transport; CD9, cluster of differentiation 9; CD63, cluster of differentiation 63; CD81, cluster of differentiation 81; LOs, large oncosomes; IFN-γ, interferon-γ; AECs, alveolar epithelial cells; DCs, dendritic cells; TGF-β, transforming growth factor-beta; GBM, glioblastoma; MDSCs, myeloid-derived suppressor cells; NK cells, natural killer cells; CCL2, CC chemokine ligand 2; MDR, multidrug resistance; P-gp, P-glycoprotein; TRPC5, transient receptor potential channel 5; HMECs, human mammary epithelial cells; ALL, acute lymphoblastic leukemia; 5-FU, 5-Fluorouracil; IECs, ileal epithelial cells; IFN-I, interferon I; IR-MVs, irradiated C6 cell-derived MVs; GPI, glycosylphosphatidylinositol; mAb, monoclonal antibody; HNSCC, head and neck squamous cell carcinoma; PKM2, pyruvate kinase M2; HCC, hepatocellular carcinoma; SMVs, saliva MVs; OSCC, oral squamous cell carcinoma; TRCs, tumor repopulating cells.

Disclosure

The authors report no conflicts of interest in this work.