Current Perspectives on the Unique Roles of Exosomes in Drug Resistance of Hepatocellular Carcinoma

Abstract

As a common malignant tumor worldwide, the prognosis of hepatocellular carcinoma (HCC) remains unsatisfactory, even though treatment methods have improved. Despite the developments in traditional chemotherapy and emerging targeted immunotherapy, the problem of recurrence and metastasis of HCC and adverse effects on survival and prognosis are still serious. Drug resistance is a daunting challenge that impedes HCC treatment. Exosomes, a class of extracellular vesicles ranging in size from 30 to 100 nm, have been the focus of recent studies. Exosomes can activate various signaling pathways and regulate the tumor microenvironment with their cargo, which includes functional lipids, proteins, and nucleic acids. Thus, they change the phenotype of recipient cells via exosome-mediated communication. Exosomes secreted by tumors or stromal cells can also transfer drug-resistant traits to other tumor cells. However, their effects on drug resistance in HCC are not completely understood. In this review, we summarize and discuss the underlying relationship between exosomes and drug resistance in HCC. In addition, we also show that exosomes may act as candidate biomarkers for predicting and monitoring drug responses and as potential targets or vectors to reverse the drug resistance of HCC.

Introduction

Hepatocellular carcinoma (HCC) is the sixth leading cause of death globally and the third leading cause of cancer-related death.¹ The five-year overall survival rate of patients with HCC is only approximately 10.1% due to the difficulty of early diagnosis, rapid progression, high rate of recurrence, and lack of effective treatment.² At present, the treatment methods for HCC are limited, with treatment still based on surgical resection. Consequently, the recurrence rate is as high as 70% in five years after Surgery, most of which occurs within two years.³ Since most HCC patients are diagnosed as late-middle-stage, survival time can only be prolonged via local radiofrequency ablation, arterial chemoembolization, radiotherapy, and chemotherapy.⁴ Some patients with advanced HCC can benefit from sorafenib, 5-fluorouracil (5-FU), adriamycin, doxorubicin, and platinum drugs.^5,6 However, the clinical effects of chemotherapy, targeted drugs, and immunotherapy that have emerged in recent years are not satisfactory. One reason is that HCC cells are prone to multiple drug resistance (MDR).⁶ Resistance to chemotherapeutic drugs such as gemcitabine, oxaliplatin, cisplatin, doxorubicin, and 5-FU is the main cause of chemotherapy failure in patients with HCC, especially in patients with advanced HCC or metastasis.⁷ HCC also develops resistance to multikinase inhibitors, such as sorafenib, and people must choose second-line targeted drugs.⁸ Thus, drug resistance of HCC leads to recurrence and poor therapeutic efficacy. Therefore, it is important to improve the efficacy of anti-tumor drugs by revealing the potential mechanisms of drug resistance in HCC.

Recently, the relationship between HCC and exosomes has become a subject of interest. Exosomes, a type of extracellular vesicle (EV) with a diameter of 30–100 nm, contain various biomolecules, such as proteins and nucleic acid.⁹ Exosomes secreted with lipid bilayers can be taken up by recipient cells via phagocytosis, endocytosis, or membrane fusion. The exosomal cargo is then released into the cells, where they perform various physiological functions.¹⁰ Exosome membrane proteins can also bind to target cell membrane proteins, thereby activating signaling pathways within the target cells and enabling intercellular signaling.¹¹ Tumor cells usually secrete more exosomes in response to changes in the microenvironment, such as pH, temperature, and cytotoxic drugs. For example, it was observed that Hep-G2 cells treated with cytotoxic drugs released exosomes containing high-level heat shock proteins (HSPs), which act as triggers for stress response and survival mechanisms.¹² In addition, exosomes serve a key role in tumor angiogenesis, epithelial-mesenchymal transition (EMT), recurrence, and metastasis.¹³ Evidence shows that exosome-mediated cellular communication is involved in drug resistance.¹⁴ Exosome studies have led to the proposal of new potential mechanisms of drug resistance. Generally, exosome-related tumor drug resistance is achieved in two ways: first, the exosomes deliver key drug resistance proteins (such as Rab27B) and RNAs (such as miR-31-5p) to other cells, inducing and enhancing their drug resistance; and second, exosomes can engulf drug molecules and excrete them extracellularly, reducing the intracellular drug concentration.^15,16 In addition, exosomes can fuse with target cells due to their low immunogenicity and high stability, making them an optimal choice as drug carriers. Yukawa et al¹⁷ proposed that the modification of exosomes led to potential clinical applications. Exosomes are reported to be involved in chemotherapeutic drug resistance, and the inhibition of exosome secretion is effective in sensitizing cancer cells to therapeutic drugs.¹³ In summary, exosomes may be a novel target for HCC therapy.

As a highly heterogeneous disease at the molecular and clinical levels, HCC includes various subtypes with different genetic, pathological and clinical behaviors.¹⁸ Exosomes mediate multiple drug resistance mechanisms to confer cytochemical resistance in HCC cells (Figure 1), suggesting that exosomes serve an extensive role in the development of HCC.^19,20 In this review, we summarize the exosomal cargo involved in the drug resistance of HCC (Table 1). In addition, we discussed the role of exosomes as tumor biomarkers and their potential applications in anti-tumor therapy.

Figure 1.

Exosomes mediate multiple drug resistance mechanisms to confer cytochemical resistance in HCC cells.

Table 1.

Exosomal Cargoes Involved in Drug Resistance of Hepatocellular Carcinoma

Classification	Cargoes	Effects	Reference
lncRNAs	lincVLDLR	Increase the expression of ABCG2 in recipient cells	[36]
	linc-ROR	Reduced chemotherapy-induced cell death in recipient cells	[41]
	lincRNA‐LVVDL	Increased expression of ABCG2	[36]
	lincRNA HOTAIR	Induced expression of ABCB1 and ABCG2	[112]
	lincRNA KCNQ1OT1	Up-regulated miR-7-5p-ABCC1	[113]
	lncRNA CTD-2116N20.1	Regulate chemoresistance related genes	[115]
circRNAs	circNFIX	Increases the expression of ABCG2 via the circNFIX-miR-132 axis	[37]
	circUHRF1	Up-regulated the expression of TIM-3, induce NK cell dysfunction.	[54]
	circFoxo3	Up-regulated miR-199a-5p-ABCC1	[114]
miRNAs	miR-32-5p	Activate the PI3K/Akt pathway and regulated angiogenesis and EMT	[39]
	miR-21	Down-regulate the expression of tumor suppressor genes PTEN and PTENp1	[40]
	miR-214	Reduce cell vitality, inhibits migration, and promotes apoptosis in vitro	[45]
	miR-199a-3p	Reverse the drug resistance of HCC to cisplatin	[46]
	miR-122	Render cancer cells sensitive to chemotherapeutic agents	[47]
	miR-146a	Promote M2 polarization and inhibit the anti-HCC function of T cells	[53]
	miR-23a-3p	Activation and upregulation of PD-L1 via PI3K-AKT pathway, induced immune escape mechanism via impairing the function of CD8+T cells	[56]
	miR-10b	Promoted the proliferation, migration and invasion of HCC cells	[65]
	miR-1247-3p	Convert normal fibroblasts to CAFs	[71]
	miR-210	Change cellular expression levels and paracrine or juxtacrine signaling	[76]
	miR-27a-3p	Enhance the activity of HCC stem cells and promote drug resistance	[77]
	miR-155	Promote EMT and mediate drug resistance	[83]
	miR-128-3p	Suppressing Bmi-1 expression	[86]
	miR-222	PTEN inhibition, p27/kip inhibition	[107]
	miR-491-3p	Induce ABCB1 expression	[108]
	miR-34a	Down-regulated ABCB1	[109]
	miR-133a	Down-regulated ABCC1	[110]
	miR-183	Up-regulated HIF-1α-ABCB1, ABCC2	[111]
Protein	HMGB1	Promote the expansion of TIM-1+Breg cell	[55]
	Heat shock protein	Enhance the cytotoxicity and granzyme B production of NK cells	[61]

Abbreviations: lncRNAs, long noncoding RNAs; HCC, hepatocellular carcinoma; EMT, epithelial-mesenchymal transition; PD-1, programmed death-1; PTEN, phosphatase and tensin homolog; ABC, adenosine triphosphate binding cassette.

Exosomes and Chemoresistance in HCC

Chemotherapy is one of the treatments for HCC, and the efficacy of drugs depends on the chemosensitivity of cancer cells. However, resistance to anti-tumor drugs remains a major challenge in HCC despite successful advances using targeted therapies.²¹ The emergence of MDR is the main cause of chemotherapy failure in HCC. The mechanisms of drug resistance in HCC are complex and diverse. Drug metabolism, changes in drug targets, DNA damage repair, imbalance between pro-survival and pro-apoptotic factors, activation of survival pathways, adaptation to the tumor microenvironment (TME), and phenotypic transition are all important causes of drug resistance.²² It is increasingly recognized that exosomes, secreted by tumor cells and possessing special transport capacity, are involved in multiple links of drug resistance, resulting in the transfer of drug-resistant phenotypes between tumor cells and non-tumor cells in HCC.²³ As crucial intercellular carriers, the secretion of exosomes is a rate-limiting step, rather than endocytosis of recipient cells.¹² This means that interfering with exosome secretion is an important mechanism for regulating the transfer of cargo between cells. The exosome-mediated chemoresistance of resistant and sensitive HCC cells is shown in Figure 2.

Figure 2.

The exosome-mediated chemoresistance between resistant and sensitive HCC cells. Exosomes transfer multi-drug resistance (MDR) transporters from drug-resistant cells to sensitive cells causing increased efflux of cytotoxic drugs via integrating MDR transporters on the cell membrane. Besides, exosomes induce increased anti-apoptotic signaling and DNA repair in the recipient cells.

Exosome-Mediated Drug Efflux and Inactivation

The accumulation of cytotoxic drugs in cancer cells is a prerequisite for drug efficacy. Therefore, the increase in drug efflux from cancer cells is a key factor leading to drug resistance in tumor cells. Exosome-mediated direct drug efflux serves a key role that cannot be ignored.²⁴ As early as 2003, Shedden et al²⁵ reported that gene expression associated with vesicle shedding correlated with chemosensitivity profiles, and their observations implicated vesicle shedding as a drug efflux mechanism potentially involved in drug resistance. Safaei et al²⁶ found that exosomes secreted from cisplatin-resistant tumor cells contained 2.6-fold more platinum than those secreted from cisplatin-sensitive cells. A recent study led by Jin¹² indicated that chemotherapeutic agents could be transferred into exosomes, stimulating exosome production or release, thus reducing drug bioactivity. They found that MCF7 cells (breast cancer cell line) with low P-glycoprotein (P-gp) levels reduced the intracellular concentration of paclitaxel by up to 80% via exosome-efflux. This phenomenon suggests a potential mechanism for chemoresistance.

As a membrane transporter, ABCB1 (also known as P-gp), belonging to the ATP-binding cassette (ABC) family, is the most prominent factor in the development of MDR.¹⁵ ABCB1 is expressed in more than 50% of cancers exhibiting MDR and is associated with the induction of chemotherapy.²⁷ Another study showed that ABCB1 could transport about 20 different cytotoxic drugs, including paclitaxel and doxorubicin.²⁸ Tadashi et al²⁹ investigated organic cation transporter (OCT)-1 and OCT3, as well as the ABC family efflux transporters MDR1/ ABCB1, multidrug resistance protein (MRP) 2, and breast cancer resistance protein (BCRP/ABCG2) and showed that the expression of transporters (particularly BCRP) is highly variable. This study shows the importance and variability of membrane transporters in intracellular and extracellular drug transport. Although a variety of MDR pump inhibitors (such as probenecid) have been developed, their clinical efficacy is unsatisfactory.³⁰ Is it possible that exosomes affect the distribution of membrane transport proteins between drug-resistant and sensitive cells, thereby inducing the production of drug-resistant proteins? There is already evidence showing that exosomes can transport drug transporters such as ABCB1 from drug-resistant cells to sensitive cells, which in turn can lead to drug resistance in sensitive cells.²⁷ Short exposure to chemotherapeutic drugs can significantly increase the release of ABCB1-containing EVs from Rab8B-mediated drug-resistant cells, and accelerate the fusion of these EVs with the plasma membrane of sensitive tumor cells by downregulating Rab5. This causes a significant enhancement of intercellular ABCB1 metastasis, thus conferring drug-resistant phenotype to sensitive cancer cells.³¹ Tang et al⁷ confirmed that exosomes from HepG2 cisplatin-resistant cells could transfer ABCB1 to various HCC-sensitive cells, including SMMC-7721 and Huh7 cells. Other efflux transporters, such as ABCB2, ABCA3, and MRP1, can also regulate drug resistance^32,33 via exosome transport. These findings provide a novel molecular mechanism for how chemotherapeutic drugs help sensitive cancer cells acquire drug resistance.

Exosomal non-coding RNAs (ncRNAs), including micro RNAs (miRNAs), long non-coding RNAs (lncRNAs), and circular RNAs (circRNAs), are dysregulated in drug-resistant cancer cells and regulate the expression of ABC transporters via various mechanisms.³⁴ Borel et al³⁵ concluded that the upregulation of ABC transporters in HCC is related to the downregulation of miRNA. A study revealed that the ABC transporter was regulated by exosomal lncRNA, and found an increase in lincVLDLR expression in exosomes released by HCC cells, which transmitted resistance via increasing the expression of ABCG2 in recipient cells.³⁶ The overexpression of exosomal circNFIX increases the expression of ABCG2 via the circNFIX-miR-132 axis, thereby promoting the resistance of glioma cells to temozolomide (TMZ). The serum exosomal circNFIX in patients with TMZ resistance increased and was associated with their prognosis.³⁷ In summary, studying ncRNAs in exosomes associated with ABC transport proteins and revealing their biological function in MDR may provide a novel theoretical basis for reversing this phenotype.

Exosome-Mediated Transfer of Pro-Survival Cargo

Cancer cells contain more exosomes than normal cells do. More importantly, the cargo of exosomes derived from cancer cells is distinct. For example, exosomes from cancer cells contain more miRNAs, which are closely associated with cancer invasion and drug resistance, than exosomes from normal cells.³⁸ A study showed that exosomes from different HCC cell lines contained various proteins and tumor-promoting RNAs.⁹ Exosome-mediated cargo transfer is regulated by various cytokines, such as vacuolar protein sortin 4 homolog A (VPS4A) and insulin-like growth factor (IGF)-1.³⁹ Fu et al²⁰ detected the expression of miR-32-5p and phosphatase and tensin homolog (PTEN; a tumor suppressor gene) in multidrug resistant cell lines (Bel/5-FU) and sensitive cell lines (Bel7402) via real-time polymerase chain reaction. The results demonstrated that Bel/5-FU transmitted miR-32-5p to Bel7402 through exosomes, which activated the PI3K/Akt pathway and regulated angiogenesis and EMT to further induce multidrug resistance. Cao et al⁴⁰ confirmed that exosomal miR-21 could downregulate the expression of tumor suppressor genes PTEN and PTENp1 (PTEN pseudogene 1), and affect the development of HCC. Recently, lncRNAs carried by exosomes have attracted increasing attention. Exosome-mediated lncRNA transport, especially linc-VLDLR and linc-ROR, promotes chemotherapy resistance in HCC.³⁹ Takahashi et al³⁶ found that linc-VLDLR was highly expressed in exosomes from malignant liver tumors, and regulated the drug resistance of recipient cancer cells to anti-tumor drugs such as sorafenib, camptothecin, and doxorubicin. Knockout of the linc-VLDLR gene reduces the viability of cancer cells and inhibits cell cycle processes. During chemotherapeutic stress, tumor growth factor (TGF)-β increases the expression of CD133+ cells partly due to the high expression of exosomal linc-ROR, which generally increases the drug resistance of HCC to chemotherapy. Considering the functional role of linc-ROR in TGF-β-dependent chemotherapy resistance, the use of siRNA to knockout linc-ROR to enhance chemotherapy-induced apoptosis and cytotoxicity may be a potential method for HCC treatment.⁴¹ Based on high-throughput sequencing, increasing evidence has shown that circRNAs are also involved in various cancer-related processes, including tumor initiation, progression, relapse, and drug resistance.⁴² Xu et al⁴³ found that exosomal circRNAs play a role in preventing the Pre-MRNA Processing Factor 19-mediated degradation of Y box-binding protein 1 (YB-1), thus affecting the expression of downstream gene targets of YB-1, including AKT, Raf1, ERK, c-Myc, and TGF-β. These exosomal RNAs also enabled the transmission of sorafenib resistance among HCC cells. These studies suggest that exosomal ncRNAs play a broad role, and blocking their functional pathways may be one of the research directions for improving the drug resistance of HCC in the future.

Exosomes also regulate drug resistance via transmitting cytokines. It⁴⁴ has been confirmed that exosomes from HCC induce sorafenib resistance via increasing the level of hepatocyte growth factor (HGF) in the TME and activating the c-Met/Akt pathway. This suggests that HGF/c-Met may be a vital target for improving sorafenib resistance in HCC. Exosomes from highly invasive tumors may lead to stronger drug resistance.⁴⁴

However, not all exosomal cargo promotes drug resistance. When exosomes rich in miR-214 fuse with cells, they reduce cell vitality, inhibit migration, and promote apoptosis in vitro. Exosomal miR-214 can also reverse cisplatin resistance of gastric cancer, which may be a potential alternative to cisplatin-refractory gastric cancer.⁴⁵ Zhang et al⁴⁶ verified that exosomal miR-199a-3p (exo-miR-199a-3p) could sensitize HCC cells to cisplatin via flow cytometry, cell counting Kit-8 (CCK-8) assay, immunofluorescence assay, and transwell assay. Another research showed that adipose tissue-derived mesenchymal stem cells (AMSCs) transfected with miR-122 could package miR-122 into secreted exosomes, which mediated the transmission of miR-122 between AMSCs and HCC cells, thereby rendering HCC cells sensitive to chemotherapeutic agents via alteration of miR-122-target gene expression.⁴⁷ These studies indicate that the functions of exosomal cargo are diverse. This poses a challenge to the use of exosomes as vehicles for antitumor drugs.

Exosomes and Immunotherapeutic Resistance in HCC

Compared with other cancers, HCC is less sensitive to traditional chemotherapy.⁴⁸ In recent years, immunotherapy has gained popularity, and a variety of drugs, such as atezolizumab, nivolumab, and pembrolizumab, have been approved for HCC patients.⁴⁹ Although immunotherapy has exhibited efficacy in the treatment of HCC, some immunotherapies, such as checkpoint inhibitors, have exhibited limited benefit for HCC patients.⁵⁰ It has been found that multiple immune checkpoints, including programmed death-ligand-1/programmed death-1 (PD-L1/PD-1), can significantly affect cancer development. PD-L1/PD-1 inhibitors have been widely used in clinics, but they do not exhibit the expected therapeutic advantages.⁵¹ This may be explained by variation in types of drug resistance. Immunosuppression and immune tolerance are key factors in the occurrence, development and metastasis of HCC. The unique immunobiology of the liver promotes tumorigenesis and tumor immune tolerance under conditions of fibrosis and chronic inflammation.⁵² Exosomes serve multiple roles in the interaction between HCC cells and immune cells, thereby mediating tumor progression and immune evasion.⁵³ It has been proven that the exosomes secreted by drug-resistant tumor cells can reshape immune cells (T cells, macrophages, and dendritic cells) in the TME, disrupting their function and preventing them from inducing host immune responses.¹⁶ The role of exosomes in immunotherapeutic resistance can not be ignored. Zhang et al⁵⁴ have found that circular ubiquitin-like with PHD and ring finger domain 1 RNA (circUHRF1) was highly expressed in HCC tissues and exosomes derived from HCC. In addition, this study demonstrated that exosomal circUHRF1 was delivered into natural killer (NK) cells and upregulated the expression of T cell immunoglobulin and mucin domain 3 (TIM-3), thereby inducing NK cell dysfunction. More importantly, HCC cells overexpressing circUHRF1 present the characteristics of anti-PD-1 therapy. Ye et al⁵⁵ showed that exosome-derived high mobility group box-1 protein (HMGB1) could promote the expansion of TIM-1+Breg cells, which mediate immune escape in HCC via the Toll-like receptor (TLR) 2/4 and mitogen-activated protein kinase (MAPK) signaling pathways, suggesting that the inhibition of exosomal HMGB1-TLR2/4-MAPK pathways could treat this immune tolerance feature of HCC. Han et al⁵³ revealed that exosomal miR-146a could promote M2 polarization and inhibit the anti-HCC function of T cells. It has been reported that endoplasmic reticulum (ER) stress causes HCC cells to release miR-23a-3p-rich exosomes. Once internalized by M2 cells, miR-23a-3p suppresses the expression of PTEN, resulting in the activation and upregulation of PD-L1 via the PI3K-AKT pathway, which induces an immune evasion mechanism via impairing the function of CD8+T cells.⁵⁶ These findings provide a novel alternative to overcome immunosuppression and immune evasion in the TME of HCC.

In addition, PD-L1 can be anchored on the surface of exosomes as a transmembrane protein and plays a vital role in immune evasion and drug resistance in immunotherapy. Exosomal PD-L1 imparts an immunosuppressive phenotype via three main mechanisms: direct endogenous exosomal PD-L1, indirect induced PD-L1, and PD-L1-mediated antagonism of immune checkpoint blockade therapy change.⁵⁷ Exosomal PD-L1 can inhibit T cell function and induce systemic immunosuppression.⁵⁸ Chen et al⁵⁹ revealed that interferon-γ (IFN-γ) could increase the level of PD-L1 on exosomes, thereby inhibiting the function of CD8+ T-cells and promoting tumor growth. Samantha et al⁵⁷ also found that the level of PD-L1 expression on exosomes is often positively correlated with the severity of cancer staging and negatively correlated with survival in a wide array of cancers, such as breast cancer and colon cancer. Conversely, tumor-derived exosomes can also express a large number of major histocompatibility complex class I molecules (MHC I) and tumor markers, such as HSP, participating in antigen presentation and T cell stimulation, to trigger a CD8+ T-cell-dependent anti-tumor response.⁶⁰ HCC cell-derived HSP-bearing exosomes can effectively enhance the cytotoxicity and granzyme B production of NK cells, upregulate the expression of inhibitory receptor CD94, and downregulate the expression of activating receptors CD69, NKG2D, and NKp44. Notably, anti-tumor drugs that cells are resistant to enhance exosome release and produce more exosome-carrying HSPs, thus enhancing the cytotoxic response.⁶¹ These studies, which arrive at contradictory conclusions, show that the functions of exosomal cargos and membrane modifiers are complex and diverse, and that targeting a single cargo cannot achieve satisfactory therapeutic effects. Further research is needed to verify whether HCC-derived exosomes affect other immune factors. The exact mechanisms underlying the immunomodulatory effects in HCC remain to be elucidated and are promising targets for future research.

Exosomes Regulate TME in the Drug Resistance of HCC

Tumor heterogeneity, recurrence, metastasis, and drug resistance are the main reasons why tumors are difficult to treat. The therapeutic efficacy of anti-tumor drugs is unsatisfactory due to insufficient targeting, severe side effects of drugs and radiotherapy, and many other challenges.⁶² This suggests that tumor treatment should not only target malignant tumor cells but also consider the effect of the TME. TME includes tumor epithelium and various tumor-supporting cells, such as immune cells, fibroblasts, immunosuppressive cells, adipocytes, endothelial cells, and various cytokines. The interaction between tumor cells and non-tumor cells in the TME is triggered via direct cell-to-cell contact and the transfer of soluble molecules (such as cytokines and chemokines), while exosomes play a key role in intercellular molecular transfer.⁶³ In addition, the interaction between TME and tumor cells is a key contributor to immune escape, recurrence, and metastasis.⁶⁴ An in-depth study of the complex exosome-mediated intercellular communication network is essential for elucidating the mechanisms that promote tumor cell growth and drug resistance. TME can also affect the release and function of exosomes. Tian et al⁶⁵ demonstrated that an acidic microenvironment triggered the activation of HIF-1/2 α and stimulated the expression of exosomal miR-21 and miR-10b, which significantly promoted the proliferation, migration and invasion of HCC cells in vivo and in vitro. Here, we summarize the latest studies to better illustrate the role of exosome and TME interactions in HCC resistance.

The impaired function of stromal cells contributes to the maintenance of cancer cells and creates a favorable TME for the growth of cancer cells.⁶⁶ Exosomes secreted by mesenchymal stem cells (MSCs) promote the progression of breast cancer via inducing the differentiation of monocytic myeloid-derived suppressor cells into highly immunosuppressive M2-polarized macrophages.⁶⁷ Zhang et al⁶⁸ reported that MSC-derived exosomes enhanced CD4+CD25+ T-cells or CD4+CD25+Foxp3+ Tregs cells in vitro and in vivo via allogeneic antigen-presenting cell (APC)-mediated pathways. Similarly, tumor-derived exosomes are involved in the differentiation of fibroblasts to cancer-associated fibroblasts (CAFs), which promotes the occurrence of tumor drug resistance.⁶⁹ For example, exosomes isolated from HCC cells exhibit a great capacity to convert normal HSCs to CAFs, because exosomal miR-21 directly targets PTEN, leading to the activation of PDK1/AKT signaling in HSCs. In addition, activated CAFs further promote tumor progression via secreting angiogenic cytokines, including VEGF, MMP2, MMP9, and TGF-β.⁷⁰ High-metastatic HCC cells, which can secrete exosomes with miR-1247-3p, exhibit a greater capacity to convert normal fibroblasts to CAFs than low-metastatic HCC cells, leading to sorafenib resistance.⁷¹ Exosomes secreted by CAFs can also develop drug resistance. Cisplatin and paclitaxel promote secretion of miR-522 from CAFs via activating the ubiquitin-specific protease 7/heterogeneous nuclear ribonucleoprotein A1 axis, resulting in the inhibition of chiradonate lipoxygenase 15 and decreased lipid peroxide accumulation in cancer cells, eventually leading to reduced chemotherapy sensitivity.⁷² These results emphasize the importance of studying the mechanisms of drug resistance induced by stromal cell exosomes.

Cancer stem cells (CSCs) are a subgroup of cancer cells with functions similar to those of normal stem cells, and they have the potential for self-renewal, unlimited proliferation, and differentiation. In addition, CSCs possess the ability to evade immune surveillance, which is closely related to tumor invasion, metastasis, drug resistance and recurrence after treatment.⁷³ CSCs can activate non-tumor cells through exosomes. Li et al⁷⁴ highlight that CSCs from esophageal squamous cell cancer secreted exosomes containing fragile X mental retardation 1-antisense RNA 1 and transfer the stem cell phenotype to recipient non-CSCs via activation of TLR7-NFκB signaling and upregulating c-Myc levels in recipient cells. CSCs exhibit chemoresistance or radioresistance due to EMT and DNA damage checkpoint activation.⁷⁵ Yang et al⁷⁶ suggested that the transfer of CSCs’ exosomal miRNAs (such as miR-210) could change cellular expression levels and paracrine or juxtacrine signaling, thus preventing the goals of chemotherapy, such as cell cycle arrest and cancer cell apoptosis. Similarly, M2 macrophage-derived exosomes with miR-27a-3p can enhance the activity of HCC stem cells and promote drug resistance.⁷⁷ Therefore, specific targeted therapy of tumor stem cells and their exosomes in the TME may improve the efficacy of anti-tumor therapy.

EMT is considered to be the process by which epithelial cells lose their epithelial phenotype (such as E-cadherin expression) and acquire more mesenchymal phenotypes (such as N-cadherin expression).⁷⁸ Tumor cells acquire mobility and invasiveness through EMT, which is the initial step in distant metastasis of cancer.⁷⁹ In addition, the emergence of CSCs is partly attributed to the EMT.⁸⁰ Evidence shows that EMT of tumor cells leads to tumor metastasis and drug resistance.⁸¹ Several important molecules, such as transcription factors (SNAIL, TWIST, and ZEB) and miRNA (miRNA-200 family, miR-15, and miR-186), which are involved in EMT and drug resistance, are considered vital. However, the connection between EMT and drug resistance has not been fully elucidated.⁸² Santos et al⁸³ analyzed the transfer ability of drug-resistant phenotypes to sensitive cells in breast cancer via MTT assay and scratch test. The results showed that exosomes could promote EMT and mediate drug resistance in sensitive cells via transmitting miR-155. Hisakane et al⁸⁴ revealed that miR-210-3p was upregulated in exosomes isolated from osimertinib-resistant HCC827, and their study found that exosomal miR-210-3p may promote EMT and induce resistance to osimertinib in HCC827 cells (a type of lung cancer cell line). Conversely, Kim et al⁸⁵ revealed that exosome-mediated miR-125b transfer disrupted TGF-β1-induced EMT and TGF-β1/SMAD signaling pathway in recipient cells via decreasing SMAD2 protein expression. In addition, exosomal miR-125b expression was downregulated after metastasis. Liu et al⁸⁶ developed a protocol for exosome-mediated miR-128-3p delivery to oxaliplatin-resistant cells in colorectal cancer. On one hand, exosomal miR-128-3p suppressed EMT via suppressing Bmi-1 expression. On the other hand, exosomal miR-128-3p reduced the efflux of oxaliplatin via inhibiting the expression of drug transporter MRP5, thus increasing intracellular oxaliplatin accumulation. Thus, exosomes can be used as a novel strategy to enhance the sensitivity to chemotherapy. In conclusion, the interaction between exosomes and TME is complex and needs to be explored constantly to provide a new orientation for overcoming drug resistance in HCC in the future. Here we summarize that, in HCC cells, exosomes, as carriers of information, mediate communication between the various cell types in TME leading to the acquisition of drug resistance (Figure 3).

Figure 3.

Transfer of drug resistance via exosomes between TME and HCC cells. (A) Exosomes loaded with a high level of miR-210-3p lead to epithelial-mesenchymal transition; (B) Cancer cells release miRNA (miR-210) containing exosomes to stimulate CSC-like features; (C). Exosomes secreted by cancer cells can promote cancer-associated differentiation in adjacent fibroblasts polarization towards a tumor-supportive phenotype; (D) Exosomes derived from cancer cells, immune cells, and other stromal cells serve essential roles in remodeling the tumor immune microenvironment.

Abbreviation: CSC, cancer stem cell.

Potential Clinical Applications of Exosomes in HCC Drug Resistance

Exosomes as Biomarkers on the Prediction of Therapeutic Response in HCC

Biomarkers can be used to predict tumor response to specific treatments and represent sensitivity or resistance to anti-tumor drugs.⁸⁷ Biomarkers for predicting treatment response in HCC have been widely studied. Yu et al⁸⁸ analyzed the transcriptional dataset of 225 HCC tissues and 220 non-HCC liver tissues from the Gene Expression Omnibus database. It was revealed that MTR4 (an RNA helicase) is overexpressed in a few HCC tissues and is an independent diagnostic marker for predicting poor prognosis in patients with HCC. Myojin et al⁸⁹ indicated that ST6GAL1, a tumor-derived secreted protein positively regulated by FGF19, is a tumor biomarker in lenvatinib-susceptible HCC. Blood-based liquid biopsy is a good method for evaluating treatment response due to its minimal invasiveness, reproducibility, and ability to dynamically evaluate specific molecular markers.

With the understanding of exosome biology and its correlation with tumor drug resistance, the unique characteristics of exosomes (surface markers, cargo, relatively stable structure and ubiquity in body fluids) and exosomal cargo constantly change with disease conditions,⁹⁰ making them attractive as potential biomarkers. On the one hand, exosomes protect molecules from degradation. Compared with circulating tumor RNAs or DNAs, the nucleic acids contained in exosomes may be more informative and reproducible. Exosomes, on the other hand, can be used to obtain information via quantification of the DNA, RNA, and proteins they carry.²⁴ Theoretically, these studies provide more accurate information for predicting the treatment response of HCC. Kim et al⁸⁵ believed that exosomal miR-125b may be a reliable biomarker for the diagnosis and evaluation of extrahepatic metastasis of HCC. Zhu et al⁹¹ established a prognosis and recurrence risk prediction model, which presented a significant predictive performance, based on two exosomal genes (MYL6B and THOC2). These findings provide a foundation for improving the early detection of HCC via identifying molecular markers. However, the application of exosomes as biomarkers remains a challenge because of the mixing of tumor-derived exosomes and normal cell-derived exosomes in the circulation.⁹²

Exosomes as Novel Therapeutic Interventions in HCC Drug Resistance

The efficacy of anti-tumor drugs is limited due to poor drug solubility, short half-life, and inefficient drug delivery, leading to drug resistance and significant systemic toxicity.¹⁶ In addition, the low efficiency of drug delivery is a vital reason for treatment failure. The drug encounters a variety of obstacles before it reaches and acts on the intended target after entering the circulation through intravenous injection.¹² To improve the chemotherapeutic efficacy of HCC, there is an urgent need to develop a drug delivery system exhibiting active targeting and achieve local, controllable, and continuous drug release. Exosomes exhibit excellent histocompatibility and engineered exosomes can specifically target tumor tissues, improve the distribution of drugs in the body, improve efficacy, protect normal cells, and minimize toxicity.⁹³ Due to the heterogeneity of exosomes from different cells, the current technology to treat tumors via exosomes is not that precise or effective, and various obstacles still need to be overcome.⁹⁴ The selection of appropriate exosomes carrying biomolecules or chemical drugs for HCC and how to effectively modify and transfer exosomes to recipient cells are of great significance. Various experiments have confirmed that the assembly of tumor cell-targeting ligands (such as peptides, antibodies, and lipids) on the surface of drug-loaded exosomes can achieve tumor-specific drug delivery and reduce non-specific toxicity.^95,96 Lin et al⁹⁷ applied iRGD-modified (iRGD: a 9-amino acid cyclic peptide) exosomes with siCPT1A, a key enzyme of fatty acid oxidation (FAO), to specifically transport siCPT1A into colon cancer cells to suppress FAO, which plays a vital role in drug resistance in cancer cells. Consequently, iRGD-modified exosomes significantly inhibited CPT1A in cancer tissues and reversed oxaliplatin resistance via inhibiting FAO with high safety. Lima et al⁹⁸ found that cytokines in TME, especially CCL2, modify cancer exosomes via binding to surface glycosaminoglycan side chains of proteoglycans, resulting in the accumulation of exosomes in specific cell subgroups and organs. The accumulation of exosomes leads to changes in the immune environment of these organs. Notably, CCL2-modified exosomes directly express CCL2 receptor CCR2, suggesting that exosome-binding cytokines are the key determinants of exosome-cell interaction. These studies also provide a reasonable strategy for the application of exosomes in the treatment of HCC. A variety of receptors and proteins, such as glypican-3 (GPC3), somatostatin receptor (SSTR), and a cluster of differentiation 44 (CD44), are relatively highly expressed on the surface of liver cancer cells and normal liver cells. Exosomes incorporated with specific antibodies targeting these proteins may help to develop an effective therapy for advanced HCC.⁹⁹ In addition to exosomes, studies have focused on the development of exosomal analogs for drug delivery.^100,101 Liu et al¹⁰² developed a drug nanocarrier for targeted chemotherapy of HCC. Structurally, the homotypic HepG2 cell membrane was used as the cloak, and a poly lactic-co-glycolic acid (PLGA) nanoparticle as the core, manufacturing the nanocarrier HepM-PLGA. Doxorubicin carried by HepM-PLGA nanoparticles exhibited high delivery efficiency and remarkable therapeutic effects in vitro and in vivo. It provides a promising nano-targeted drug delivery system for drug-resistant HCC. However, targeted delivery applications based on HCC cell surface proteins are rare, and there should be studies on antigen-directed exosome delivery.

In this promising new era of cancer immunotherapy, cancer vaccination is the ultimate goal.¹⁰³ The latest research shows that exosomes secreted by HCC antigen-modified dendritic cells (DCs) can be used as cell-free vaccines. The findings of Lu et al¹⁰⁴ proved that AFP-enriched dendritic cell-derived exosomes (Dexs) could trigger effective antigen-specific anti-tumor immune responses and reshape the TME of HCC, as demonstrated by significantly increased γ-IFN-expressing CD8+T lymphocytes, elevated levels of γ-IFN and IL-2, and fewer CD25+Foxp3+Tregs and decreased levels of IL-10 and transforming growth factor-β in tumors. Li et al¹⁰⁵ revealed that Dexs loaded with recombinant adeno-associated viral vector (rAAV)-carrying AFP gene (rAAV/AFP) can effectively stimulate the proliferation of T cells and induce the activation of T cells into antigen-specific cytotoxic T lymphocytes (CTL) exhibiting an immune response against liver cancer. In addition, it seemed that Dex-sensitized DC precursors could trigger MHC I-restricted CTL responses more effectively, maximizing specific immune responses against HCC. These studies show that Dexs, which present the advantages of dendritic cells and cell-free vectors, can partially replace mature DCs as tumor vaccines or natural anti-tumor adjuvants. It provides a novel alternative for HCC therapy.

Conclusions and Perspective

Cancer is not only a large number of malignant cells, but also a complex “rogue” organ, in which different types of cells, such as fibroblasts, adipocytes, immune cells, and tumor vascular system cells, are involved in tumor homeostasis.¹⁰⁶ Anti-tumor drug resistance caused by a series of physiological activities has been an obstacle to cancer treatment for a long time. Although significant progress has been made in modern anti-tumor drugs, the occurrence of drug resistance often leads to the failure of HCC treatment. In addition to existing chemotherapy and emerging immunotherapy, there is an urgent need to develop new methods to eliminate tumor progression and recurrence caused by drug resistance. To explore effective new treatments, we must study the role of tumors and their microenvironment, including lymphocytes, macrophages, myeloid suppressor cells, and their exosomes in drug resistance. Exosomes have the unique potential to capture the dynamic complexity of cancer and can be used to test a variety of biological components associated with HCC resistance in real-time. At present, our understanding of exosome physiology, release, transport, internalization, and transport mechanisms is limited, and the mechanism of interaction and modification between exosomes and recipient cells also requires more comprehensive research.⁵³ Even though there are various challenges, exosomes may be used as a candidate biomarker to predict and monitor the efficacy of treatment in patients with HCC, and as a potential target or vector to reverse drug resistance, which serves a vital role in tumor detection, prediction and treatment in the future.

Disclosure

The authors report no conflicts of interest in this work.