Non-coding RNAs shuttled via exosomes reshape the hypoxic tumor microenvironment

Accumulative evidence suggests that tumor cells behave differently depending on extrinsic factors of the surrounding microenvironment. Distinct types of cells including immune cells, fibroblasts, and endothelial cells interactively communicate to facilitate cancer progression [4]. Additionally, pH, reactive oxygen species (ROS), inflammation, components in the extracellular matrix (ECM), and hypoxia can influence the metabolism and aggressiveness of cancer [5‐8]. Therefore, the various interplay between cellular and non-cellular factors in the tumor microenvironment may serve as potential therapeutic targets in the clinical settings.

Irregular vessel formation and the rapid proliferation of cancer cells create hypoxic conditions in malignant tumors. In this regard, hypoxia is a common feature in the microenvironment of most solid tumors [9]. Clinical studies have revealed that overexpression of hypoxia-induced genes is associated with poor prognosis in many cancer types including pancreatic, lung, breast, prostate, and ovarian cancer [10‐14]. Besides, plentiful in vitro and in vivo experimental data have suggested that hypoxia orchestrates malignant phenotypes of cancer cells through activation of multiple oncogenic signaling pathways. Transcription factors and epigenetic regulators can concertedly exert reinforcement of oncogenic signaling pathways, controlling the expression of numerous genes under hypoxia. Nevertheless, interactions between cancerous cells and non-cancerous cells could be further invigorated in the hypoxic tumor microenvironment. Cancer cells stimulated by hypoxia manifest increased drug-resistance, tumorigenesis, angiogenesis, invasiveness, and immune suppression [15].

Several decades ago, oxygen sensing mechanisms at the molecular level had been discovered that some transcription factors play a central role in tissues in response to low oxygen tension (< 10 mmHg) [16]. The vital proteins involved in the process of cellular adaptation under hypoxia are hypoxia-inducible factor-1 (HIF-1), prolyl hydroxylase (PHD), and von Hippel-Lindau (VHL). HIF-1α is a transcription factor constitutively activated in response to hypoxia [17]. Under normal oxygen tension (45–65 mmHg) at peripheral tissues, PHD is activated, adding a hydroxyl group to HIF-1α at a proline residue. Hydroxylated HIF-1α is then subjected to degradation through ubiquitination, mediated by the VHL complex. Unlike HIF-1α, its binding partner, HIF-1β is stably expressed even at the high oxygen tension. Under hypoxic conditions, the accumulated dimer of HIF-1α and HIF-1β bind to hypoxic response elements (HREs) of various genes in the nucleus. Activated HREs are closely associated with oncogenic phenotypes such as proliferation, invasion, epithelial-mesenchymal transition (EMT), and metabolic reprogramming [16]. Furthermore, recent studies have illustrated that myriad epigenetic modifications are involved in hypoxic signals through histone modifications and DNA methylation [18, 19].

The hypoxic conditions also affect interactions between cancerous and non-cancerous cells in the tumor microenvironment. Hypoxia-induced overexpression of programmed death-ligand 1 (PD-L1) in cancer cells disabled cytotoxic functions of programmed cell death protein 1(PD-1) positive activated T lymphocytes [20, 21]. Moreover, HIF-1α promoted the overexpression of PD-L1 in myeloid-derived suppressor cells (MDSCs) and macrophages, neutralizing anti-cancer immunity in the tumor microenvironment [22]. Additionally, hypoxia upregulated V-domain Ig suppressor of T cell activation (VISTA) in MDSCs, thereby suppressing T cell activity [23]. CD47 enriched at the plasma membrane of hypoxic tumors inhibited the phagocytic activity of macrophages [23, 24]. Along with hypoxia-induced changes in the tumor immune microenvironment, hypoxia can assist tumor growth by reprogramming fibroblasts. In the study which utilized the cancer-associated fibroblast (CAF)-endothelial cell co-culture model, hypoxic CAFs promoted angiogenesis through NCBP2-AS2-mediated vascular endothelial growth factor A (VEGFA) secretion [25]. In line with the result from the CAF-endothelial co-culture study, another study demonstrated that CAF induced angiogenesis via recruitment of HIF-1α and G-protein estrogen receptor (GPER) to the promoter region of VEGF [26]. Moreover, pancreatic CAFs produced more insulin-like growth factor 1 (IGF1), and cancer cells increased the expression of IGF1 receptor (IGF1R) in response to hypoxia. This specific hypoxia-potentiated CAF-cancer cell communication promoted the metastatic ability of pancreatic cancer cells [27]. A multi-center study from Norwegian hospitals suggested that upregulation of miRNA-210, a hypoxia-induced miRNA, in CAFs but not in cancer cells was negatively correlated with the prognosis of prostate cancer patients [28]. Therefore, hypoxic responses of both cancerous and non-cancerous cells are vital determining factors of cancer progression.

Transcriptomic and epigenetic landscapes of a tumor are vastly changed by hypoxia. As recent studies have underscored the importance of exosomes as a critical mode of cell-to-cell communication, it would be worthwhile to unveil how exosomal non-coding RNA signaling regulates the hypoxic tumor microenvironment.

Extracellular vesicles (EVs) are secreted by almost all cell types into the extracellular space. EVs are classified into microvesicles, apoptotic bodies, exosomes, etc., according to their intracellular origin, size, and biogenesis [29]. Exosomes are endogenous vehicles with a size of 40–150 nm in diameter. Endocytic vesicles produced in the plasma membrane can form early-endosomes by continuous endocytosis and develop into late-endosomes. Late-endosomes bud inwards to form multi-vesicular bodies (MVBs), and the fused MVBs with the plasma membrane enable the release of intraluminal vesicles (ILVs) into extracellular space, called exosomes [30]. The endosomal-sorting complex required for transport (ESCRT) machinery is necessary for exosome formation at endosomes. It is complicated protein machinery comprised of four protein ESCRTs (0 through III) regulating MVB formation, vesicle budding, and cargo sorting [31]. However, some studies have revealed an ESCRT-independent exosomal cargo sorting manner, suggesting that the mechanisms are broader and more intricate.

Exosomes are mediators of cell-cell interactions in that they are capable of delivering functional mRNAs, microRNAs (miRNAs), DNAs, and proteins to recipient cells altering their physiological and pathological functions. These exosomal cargos are enclosed inside the double membrane and are stable to environmental factors such as nucleases, proteases, and oxidative stress so that they can be delivered to recipient cells in an efficient and intact manner [32, 33]. Cancer cell-derived exosomes affect cancer progression such as proliferation, drug resistance, and metastasis [34]. Meanwhile, these tumor-derived exosomes also have a significant impact on various stromal cells in the tumor microenvironment. They are involved in the function of endothelial cells, the polarization of macrophages, regulation of T cells, and suppression of natural killer cells (NK cells) activity and other biological activities [35‐38]. Stromal cell-secreted exosomes, in turn, can support the malignant phenotypes of cancer cells. For instance, tumor-associated macrophage (TAM)-derived exosomes containing functional factors promoted migration and invasion in breast cancer [39]. CAF-derived exosomes conferred chemoresistance to ovarian cancer cells [40]. Therefore, exosomes may play a pivotal role in the inter-tumor cell, inter-stromal cell, and tumor-stromal cell interactions.

Additionally, exosomes have been detected in almost all types of body fluids such as blood, urine, saliva, breast milk, and ascites. They can be used as biomarkers to diagnose diseases in non-invasive or minimally invasive ways [41]. Furthermore, exosomes can be used as natural nano-carriers for therapeutic applications that can efficiently deliver various signaling molecules. Exosomes show similar structures to a bilayer of lipids of cell membranes because they fuse to the plasma membrane during secretion. Recent researches have shown the possibility that exosome-mediated delivery of small interfering RNAs (siRNAs), antioxidants, anticancer drugs, and CRISPR/Cas9 system via low immunogenicity [42‐45].

RNAs are classified into protein-coding RNAs and non-coding RNAs according to their protein-coding abilities. Based on the Francis Crick’s “the central dogma of molecular biology,” many studies have focused on processes of protein production through messenger RNA (mRNA) and constituent RNAs such as ribosomal RNAs (rRNAs) or translators of codon sequence (tRNA) [46, 47]. However, results from human genome sequencing found that only ~ 200,000 RNAs could encode proteins, comprising only 2% of the genomes [48]. In 1965, scientists discovered a new type of regulatory non-coding RNAs that do not function through protein translation [49]. Non-coding RNAs are divided based on the number of nucleotides constituting the RNAs: small non-coding RNAs including miRNAs, siRNAs, piwi-interacting RNAs (piRNAs) composed of less than 200 nucleotides, and lncRNAs with more than 200 nucleotides in size [50]. In addition, another type of non-coding RNAs highly represented in the eukaryotic transcriptome is circRNAs, which form covalently closed continuous loop structures, unlike the abovementioned linear RNAs. CircRNAs are relatively stable compared to linear non-coding RNAs. Exosomes contain a variety of RNA species, among which miRNAs are the most abundant and surely most intensively studied while lncRNAs and circRNAs are also becoming research hotspots now. Some qualitative and quantitative assays have revealed the asymmetric distribution of RNAs between cells and cell-derived exosomes. This phenomenon has boosted many interesting hypotheses, suggesting that RNA molecules are not randomly packaged in exosomes but with a set of sorting systems involved.

A single mammalian cell carries approximately 100,000 endogenous miRNAs, while a single exosome contains about 500 miRNAs. Pigati et al. found that the abundance of about 66% of extracellular miRNAs well reflected the corresponding abundance of miRNAs in the cells [51]. van Balkom et al. also reported that the most abundant exosomal miRNAs closely corresponded with the most abundant cellular miRNAs [52]. These findings suggest that the majority of high expressed miRNAs are encapsulated and secreted via exosomes passively for an osmotic-like effect. However, there was still a category of miRNAs that might be selectively retained or released. For example, more than 90% of the mature miR-451, which is functioned as a tumor suppressive gene in breast cancer, was found to be exported into extracellular space [52]. In addition, Hannafon et al. observed that miR-451, miR-122, miR-1246, and miR-21 were more enriched in the breast cancer cell-derived exosomes than normal epithelial cell-derived exosomes. Intriguingly, oncogenic miR-1246 and miR-21 showed consistent high abundancy in the cells while tumor suppressive miR-451 and miR-122 were downregulated in cellular expression [53]. Based on these studies, it can be inferred that apart from the passive osmotic-like pattern, the function-dependent selective mechanism may be present when RNAs are secreted via exosomes. Cells might tend to secrete RNAs that are unnecessary, advantageous, or even harmful for sustaining cell properties. Ragusa et al. further strengthened and developed this point. They found that in addition to tumor suppressive miRNAs, immunosuppressive miRNAs were also highly abundant in exosomes compared to cells, which indicated that RNAs might be selectively released into the tumor microenvironment to influence the immune response [54].

Some lipids and proteins have been demonstrated to be involved in sorting specific non-coding RNAs into exosomes. The neural sphingomyelinase 2 (nSMase2) was reported to be associated with the secretion of exosomes, which was also the first molecule found to guide miRNAs into exosomes. The expression of nSMase2 was positively related to the level of exosomal miRNAs [55]. Besides, some important proteins might also impact the RNA selective sorting process. Argonaute 2 (Ago2), a component of the miRNA-induced silencing complex (miRISC), was implicated in the assortment of several miRNAs into exosomes. Additionally, Alix, an accessory protein of ESCRT, was reported to be involved in the release of exosomal miRNAs from liver stem-like cells through interacting with Ago 2 [56]. It has been reported that hypoxia could inhibit the Ago2 degradation by mediating hydroxylation of Ago2 by C-P4H(I) and increase the various functions of it, indicating the possible regulative role of hypoxia in sorting miRNAs into exosomes [57]. Villarroya-Beltri et al. identified that some short motifs were overexpressed in exosomal miRNAs and mRNAs. The protein heterogeneous nuclear ribonucleoprotein A2B1 (hnRNPA2B1) could bind to those motifs and modulate RNAs loading into exosomes. Moreover, this process was controlled by the sumoylation of hnRNPA2B1 [58]. Besides, hnRNPA2B1 was also reported to be involved in the encapsulation of lncARSR into exosomes [59]. Kossinova et al. detected several structural motifs enriched in exosomal lncRNAs and mRNAs using bioinformatics approaches. Cytosolic Cold shock protein YB-1 and RNA methyltransferase NSUN2 could recognize these motifs and mediate sorting specific lncRNAs and mRNAs into exosomes [60]. YB-1 was reported to be physically interacted with HIF-1α and regulate the transcription of hypoxia-dependent genes [61]. In addition, YB-1 could enhance the expression of HIF-1α and promote the invasion and metastasis in sarcoma [62]. Li et al. showed more abundant circRNAs were present in exosomes compared to the source cells by RNA-sequencing analyses for the first time. The level of exosomal circRNAs and cellular circRNAs were only moderately correlated, suggesting that certain circRNAs might be actively incorporated into exosomes while some might be selectively retained in cells. CircRNAs have been reported to be capable of binding to miRNAs working as miRNA sponges. The authors also demonstrated that the selective sorting of circRNAs was associated with the relevant miRNAs [63]. Overall, non-coding RNAs with certain sequences may favor themselves loading into exosomes, whereas a bunch of protein complexes or lipids might be involved as well. However, there is still a lack of ample evidence that fully illustrates the underlying mechanism of the RNA sorting process, and further investigations are deserved.

Hypoxia can activate various pathways to promote the secretion of exosomes and alter the components loaded in exosomes (Fig. 1). Rab GTPases such as Rab27a and Rab27b are essential for exosomal secretion pathways in cancer cells [64]. In hypoxic conditions, altered protein expression of small GTPase in cells promotes endocytosis, consequently changing the degree of exosomal secretion [65]. In ovarian cancer, hypoxia significantly promoted exosome secretion through the upregulation of Rab27a. These hypoxia-induced exosomes elicited a more aggressive and chemoresistant phenotype of cancer cells [66]. King et al. also confirmed that hypoxic breast cancer cells produced a higher level of exosomes in a HIF-1α-dependent manner [67]. Rab5 could regulate vesicle-mediated transportation from the cell membrane to early endosomes and early endosome fusion [68]. Under hypoxia, Rab5 was clustered in the perinuclear region while CD63 showed higher co-localization with the actin cytoskeleton of prostate cancer cells, suggesting that hypoxia could enhance exosome secretion through promoting early endosome formation and fusion of multivesicular endosomes with the plasma membrane [69].

The hypoxic conditions not only boost the release of exosomes but also influence the molecules contained within exosomes. Hypoxia-induced exosomes exhibit different patterns of various molecules depending on origin cells and environmental factors. In highly malignant brain tumor glioblastoma multiforme (GBM), hypoxic cancer cell-derived exosomes showed enrichment in hypoxia-associated mRNAs and proteins (e.g., matrix metalloproteinases, IL-8, platelet-derived growth factor (PDGF), caveolin 1, and lysyl oxidase) and activated vascular cells in a hypoxia-dependent mode during cancer progression [70]. Recent studies have shed light on the exosomal non-coding RNA expression and function shift in the hypoxic tumor microenvironment. Especially with the development of sequencing technology, more and more significant non-coding RNAs are being uncovered. It has been reported that miR-21, miR-23a, and lncRNA-UCA1 were upregulated in the exosomes derived from hypoxic cancer cells and promoted cancer progression in various signaling pathways [71‐73]. Hypoxia was also reported to regulate the expression of circRNAs. Boeckel et al. first identified that cZNF292, cAFF1, and cDENND4C were upregulated while cTHSD1 was under the hypoxic condition in endothelial cells. Moreover, cZNF292 exhibited proangiogenic activities in vitro [74]. While in cancer, hypoxia could induce the expression of circDENND2A, which could promote the migration and invasion of glioma cells through sponging miR-625-5p [75]. The expression of circHIPK3 was reported to be upregulated in hypoxic exosomes compared with normoxic exosomes derived from cardiomyocytes. It could regulate the oxidative damage in cardiac microvascular endothelial cells by inducing miR-29a/IGF-1 signaling pathway [76]. This is the only report by now focusing on circRNAs in hypoxic exosomes. There is no direct evidence showing the role of hypoxic exosomal circRNAs in cancer yet. Collectively, non-coding RNAs have been reported to exert various functions in translation, RNA splicing, DNA replication, etc. [77‐80]. Further investigations are warranted to comprehensively understand the role of non-coding RNAs in the tumor microenvironment.

Hypoxia alters tumor metabolism and transcription such as a shift to glycolysis and self-sufficient release of growth signals [98]. Even though much has been known about hypoxia-secreted metabolites promote tumor growth, the importance of hypoxic exosome-mediated tumor growth has been recently grown. Accumulating evidence indicates that pro-tumorigenic molecules secreted through exosomes in the hypoxic tumor microenvironment can promote tumor cell survival and proliferation.

MiR-210 is a well-recognized hypoxia-induced miRNA involved in various biological processes of cancer progression. It was reported to be upregulated in many types of solid tumors and related to unfavorable clinical outcomes of patients [99]. In breast cancer, miR-210 was significantly elevated in the exosomes derived from hypoxic cancer cells than those from normoxic ones [67]. Tang et al. utilized a breast cancer cell spheroid culture model to enrich highly malignant breast cancer stem cells (BCSCs). They corroborated that miR-210 was remarkably upregulated in hypoxic spheroid cells and spheroid-derived BCSCs compared to parental cells. The upregulation of miR-210 promoted the proliferation, self-renewal, and migration of BCSCs [85]. Furthermore, Yu et al. reported that miR-1273f upregulated in hypoxic tumor-derived exosomes promoted cancer proliferation of hepatocellular carcinoma (HCC) by inhibiting LHX6/Wnt/β-catenin pathway [89]. In another research of HCC, Patel and his colleagues showed that hypoxic tumor-derived exosomes reduced cancer cell viability with the increased expression of lncRNA-RoR. Knockdown of lncRNA-ROR induced expression of its target, miR-145, thus decreasing p70S6K1 (RPS6KB1) phosphorylation, PDK1, and HIF-1α expression [90]. Wozniak et al. identified a set of differentially expressed exosomal miRNAs in hypoxic conditions. Hypoxia upregulated miR-494-5p, miR-4497, miR-513a-5p, and miR-6087 while downregulating miR-125b-5p, miR-21-5p, and miR-3934-5p in the exosomes from patient-derived melanoma cell lines cultured under hypoxia. Pathway analysis with bioinformatical tools has shown that these miRNAs were closely associated with tumor survival, but no further experimental validation was carried out [100].

Therefore, exosome-mediated communication plays an essential role in the hypoxic environment. Hypoxic exosome-shuttled bioactive non-coding RNAs have been shown as critical regulators of cancer proliferation.

Hypoxia has been demonstrated to regulate the invasion and migration ability of cancer cells mainly by promoting EMT. EMT is involved in carcinogenesis and endows transformative properties to cancer cells by improving mobility, invasion, and migration [101]. During EMT, downregulation of epithelial markers (E-cadherin and β-catenin) and upregulation of mesenchymal markers (N-cadherin and vimentin) can occur, which then induce the mesenchymal phenotypes and enhance the metastatic ability of the cancer cells. Much attention has been drawn to exosomal non-coding RNAs in the hypoxic tumor microenvironment, given that they could govern metastatic and invasive capability of cancer cells by directly or indirectly targeting EMT markers. Li et al. reported that miR-21 increased in hypoxia-derived exosome promoted invasion and migration in oral squamous cell carcinoma (OSCC) by inducing EMT [72]. In addition, lncRNA-UCA1 was present at a high level in the hypoxic exosomes from cancer cells than normoxic exosomes. The lncRNA-UCA1 secreted by hypoxic cancer cells promoted tumor progression through upregulating EMT in vivo and in vitro in bladder cancer [73]. Exosomal miR-25-3p released from hypoxic breast cancer cells stimulated migration and proliferation of tumor cells by inducing IL-6 secretion and activating NF-κB signaling in macrophages. In vivo experiments revealed that injection of breast cancer cells with the miR-25-3p inhibitor substantially reduced the tumor size by inhibiting IL-6-mediated STAT3 activation [88].

Stromal cells are also indispensable components in the tumor microenvironment. Stromal-cancer or stromal-stromal interactions mediated by exosomes have profound impacts on metastasis initiation and cancer progression. Zhang et al. demonstrated that cancer cells could uptake exosomes derived from hypoxic bone marrow-derived mesenchymal stem cells (BMSCs) and acquire higher invasiveness. During this process, miR-193a-3p, miR-210-3p, and miR-5100 transferred into cancer cells and activated STAT3 signaling, thus inducing EMT in lung cancer cells. Furthermore, these three miRNAs were upregulated in the plasma-derived exosomes of patients than non-metastatic patients [86].

Metastatic colonization is profoundly affected by the hypoxic tumor microenvironment. Tumor-derived exosomes can reflect the hypoxic characteristics of the originating cell and also are capable of facilitating pre-metastatic niche formation by transmitting non-coding RNAs. Notably, organ-specific metastasis has gained much attention in recent years. Despite the hard work of many scientists, still little has been known about the mechanisms. Exploring exosomal non-coding RNAs could give rise to promising therapeutic targets as well as prognostic biomarkers of cancer metastasis.

Resistance to anti-cancer therapies is one of the biggest obstacles in cancer treatment. Intrinsic resistance arises because of genetic alterations, whereas extrinsic resistance due to interactions between tumor cells and microenvironment against chemotherapy. Hypoxia affects the overall course of the tumor including responses to therapies. Hypoxia-induced malignancies could form resistance to various anti-cancer drugs including cisplatin, doxorubicin, sorafenib, etoposide, paclitaxel, and gemcitabine [102]. Also, researches have shown that anti-cancer drug resistance can be restored through inhibition of hypoxia-induced signaling pathway. Hypoxia could regulate chemoresistance of cancer cells by controlling cell cycle, autophagy, senescence of cells, and chemotherapeutic efficacy through acidity as well as drug efflux pump expression [103]. Hypoxia-induced intracellular substances such as proteins and non-coding RNAs via exosomes secretion affect tumor microenvironment and cancer cell chemoresistance.

Dong et al. demonstrated that hypoxic non-small-cell lung cancer (NSCLC) cell-derived exosomes enhanced cisplatin resistance of normoxic cancer cells through transmitting miR-21. Mechanically, miR-21 in hypoxic exosomes downregulated phosphatase and tensin homolog (PTEN) and PI3K/ATK pathway sequentially, triggering cisplatin resistance in normoxic cancer cells. Further analysis with the TCGA database showed that miR-21 expression was positively correlated with HIF-1α and high miR-21 expression indicated worse survival in patients undergoing chemotherapy [83]. Patel and his colleagues found linc-RoR, a stress-responsive lncRNA, regulated chemosensitivity of HCC cells to sorafenib, and doxorubicin. They described that linc-ROR expression was enhanced in the hypoxic cancer cell-derived exosomes. TGF-β enriched linc-RoR within exosomes, resulting in suppression of chemotherapy-induced cell death and tumor-initiating cell proliferation [91].

It is noteworthy that chemoresistance does not arise intrinsically in cancer cells. Many stromal cells like CAFs also support cancer cells to gain resistance to chemotherapy. MiR-223 was demonstrated to promote proliferation and invasiveness of ovarian cancer cells by targeting SOX11 expression [104], and it was the most significantly upregulated miRNA in the recurrent serous ovarian cancer tissues as compared to the primary tissues [105]. On this basis, Zhu et al. observed the upsurge of miR-223 in TAMs and TAM-derived exosomes under hypoxia. MiR-223 conveyed by hypoxic exosomes could reduce apoptosis, increase cell viability, and also increase drug resistance of ovarian cancer cells via downregulating PTEN expression and activating PI3K/AKT signaling pathway. Moreover, higher miR-223 expression was shown in the cisplatin-resistant patients and recurrent patients in the epithelial ovarian cancer (EOC) patient-derived specimens. High expression of miR-223 together with low expression of PTEN indicated a bad prognosis of ovarian cancer patients [96].

These studies indicated chemoresistance could be passed through transmitting non-coding RNAs in exosomes in the hypoxic microenvironment. Blocking chemoresistance-associated exosomal non-coding RNAs could be a promising way to overcome chemoresistance.

In principle, tumor development can be monitored by cytotoxic innate and adaptive immune cells. However, as the tumor develops from dysplasia to clinically detectable tumors, cancer cells evolve different mechanisms such as losing expression of tumor antigens or modifying immune checkpoint molecules in order to avoid the destruction by the immune system [106]. Tumor-derived exosomes have been shown to induce tumor-specific or nonspecific immune responses. Antigen-presenting cells could uptake tumor-associated antigens shuttled in exosomes and stimulate the tumor suppressive reactions [107]. Hypoxic tumor exosomes have been demonstrated to suppress T cell proliferation and NK cell activation, induce macrophage M2 polarization and regulatory T cells (Tregs) activation, and increase MDSC population resulting in immune dysfunction.

The interactions between tumor cells and T cells are critical in tumor immune microenvironment. Tumoral exosomes carrying biologically active non-coding RNAs transmit signals between cells, promoting tumor progression and immune escape. Ye et al. first reported that nasopharyngeal carcinoma (NPC) cell-derived exosomes impeded T cell dysfunction through differential miRNA expression [108]. Building on this study, they further identified that tumoral exosomes could hamper T cell function by miR-24-3p delivery. Mechanistically, hypoxia-induced exosomal miR-24-3p inhibited T cell proliferation and Th1, Th17 differentiation and inducing Treg differentiation by targeting FGF11 followed by the upregulation of p-ERK, p-STAT1, p-STAT3, and downregulation of p-STAT5 [95].

T cell exhaustion is characterized as the upregulation of PD-1 on T cells. Blocking the PD-1/PD-L1 axis is the best way to reinvigorate T cell function [109]. γδ T cell is a unique lymphocyte population that has been reported to have either anti- or pro-tumoral functions. Li et al. revealed that normoxic OSCC-derived exosomes stimulated the γδ T cell expansion and cytotoxic function in a dendritic cell (DC)-independent manner, which could be attenuated by miR-21-enriched hypoxic exosomes. MDSCs are a heterogeneous immunosuppressive cell population from myeloid lineage migrating to the tumor site through circulation [110]. A chronic inflammatory environment rich in cytokines like TNF, TGF-β, and IL-10 triggers myeloid cells converting to MDSCs. Therefore, they are normally present in cancer or chronic inflammation-associated diseases while not present in a steady state of healthy people [111]. MDSCs suppress the adaptive and innate immunity through inhibiting T cell activation, promoting M2 polarization of macrophages, inducing CAF differentiation and inhibiting NK cell cytotoxicity, thus contributing to tumor angiogenesis, metastasis, and drug resistance [112]. The accumulation of MDSCs was shown to be correlated with poor clinical outcomes and reduce the efficacy of immunotherapy in cancer patients. Hence, eliminating and suppressing MDSCs is becoming a new therapeutic strategy [113]. It was reported that exosome-shuttled miR-21 secreted from γδ T cells could abate the function of MDSCs in a PD-L1-dependent manner through targeting PTEN [82]. This study sheds new light on the effects of tumor-derived exosomes on the γδ T cells. Meanwhile, it also suggested that integrative inhibition of hypoxia-induced exosomal miRNAs and PD-1/PD-L1 axis would be a new insight in immunotherapy. In glioma, hypoxia-induced exosomal miR-21 and miR-10a presented the remarkable effects on the expansion and function of MDSCs in vitro and in vivo via miR-21/PTEN/PI3K/AKT and miR-10a/RORA/IκBα/NF-κB axis respectively [81].

Hypoxia in the tumor microenvironment could stimulate immunosuppressive effects attenuating cytotoxic T lymphocyte (CTL) and NK cell-mediated tumor cell lysis. Berchem et al. elucidated that lung cancer cells generated exosomes with higher miR-23a expression, which could impair NK cell cytotoxicity and NK cell function by directly targeting CD107a. Furthermore, higher TGF-β in the exosomes might partly contribute to the enrichment of miR-23a. This is the first study demonstrating how cancer cells in the hypoxic microenvironment educate NK cells through exosome transmitted non-coding RNAs [35].

Macrophages can be roughly classified into M1 (classically activated) macrophages with pro-inflammatory effects and M2 (alternatively activated) macrophages with anti-inflammatory effects. M1 macrophages characterized by the expression of the inducible type of nitric oxide synthase (iNOS) are proinflammatory, whereas M2 macrophages express high level of anti-inflammatory cytokines (e.g., IL10) and a potent arginase-1 (Arg1) activity to favor tumor cell growth [114]. TAMs constitute a predominant population of immune-related stromal cells in the tumor microenvironment. TAMs were previously described as exhibiting M2-like function. However, studies argue that TAMs can express hallmarks of both M1 and M2 polarization [115]. Cancer cells under hypoxia pressure secreted more functional exosomes acted as a bridge between cancer cells and macrophages, especially inducing M2 polarization. Although M2 polarization is still the mainstream, altering TAMs to a predominantly M1 phenotype has been put on the agenda for developing new immunotherapeutic strategies. These results suggest that hypoxic exosomes are influential elements in the tumor microenvironment mediating the interactions between cancer cells and macrophages.

Hypoxic EOC cell-derived exosomes containing high levels of miR-940 stimulated the M2 polarization of macrophages. Then, miR-940-induced M2 macrophages, in turn, promoted EOC cell proliferation and migration. Interestingly, a high level of miR-940 was also observed in the malignant ascites-derived exosomes compared with benign peritoneal fluids [36]. The same research team further explored the different miRNA expression profiling patterns between cancer cell-derived exosomes under hypoxia and normoxia. MiR-21–3p, miR-125 b-5p and miR-181 d-5p were selected as HIF-1α and HIF-2α induced miRNA candidates and then validated to affect macrophage M2 polarization through regulating SOCS4/5/STAT3 pathway [84]. Moreover, exosomal miR-301a-3p derived from hypoxic pancreatic cancer cells promoted macrophage M2 polarization through downregulation of PTEN expression and activating PI3Kγ signaling pathway, triggering the secretion of TGF-β, IL-10, and arginase from pancreatic cancer cells, which in turn facilitated EMT and lung metastasis [97]. Quantitative proteomics revealed that hypoxic mouse melanoma cell-derived exosomes were rich in immunomodulatory proteins and chemokines including CSF-1, CCL2, FTH, FTL, and TGFβ. Meanwhile, they detected that miRNA let7a was decreased in the hypoxic cells but dramatically increased in the released exosomes. Let7a-loaded exosomes enhanced mitochondrial oxidative phosphorylation system (OXPHOS) in macrophages through suppressing the insulin-AKT-mTOR signaling pathway [93].

Hypoxia pressure promoted the production and secretion of immune-modulating exosomes rich in non-coding RNAs. Exosome-mediated cancer-immune cell communication substantially impacts the immune reaction. Immune checkpoints are accessory molecules with T cell activation or inhibition effects. Blockage of cytotoxic T lymphocyte antigen 4 (CTLA-4) and PD-1 have heralded the dawn of an immune therapy era. Exosomal non-coding RNAs might be the indispensable targets for immune therapy based on their immune regulating functions.

Angiogenesis refers to a new blood vessel-forming process and is an essential mediator for tumor progression. Hypoxia is one of the key factors in tumor angiogenesis. Vascular immaturity and weakened cell association of tumor blood vessel network can lead to excessive permeability, poor perfusion, and increased hypoxia [116]. Angiogenesis is a complicated process comprising of many genes, regulators, and pathways. VEGF is the crucial pro-angiogenetic growth factor stimulated by the alarm of hypoxia. Carmeliet et al. found that the hypoxic induction of VEGF decreased significantly in mouse embryonic stem cells by inhibiting HIF-1α [117]. In addition to VEGF, HIF-1α is capable of regulating some other angiogenesis-associated factors like platelet-derived growth factor (PDGF-B), vascular endothelial growth factor receptor-1 (VEGFR-1), endothelin-1, iNOS, and epidermal growth factor (EGF).

Recent studies have demonstrated that exosomal non-coding RNAs under hypoxic conditions could contribute to the angiogenesis process. For instance, miR-210 upregulated both in hypoxic leukemia cells and exosomes enhanced tube formation in endothelial cells [37]. In NSCLC, HIF-1α-induced microvascular miR-494 promoted angiogenesis both in vitro and in vivo through downregulating PTEN and activating Akt/eNOS pathway [92]. Another study in lung cancer showed that hypoxic exosomes promoted angiogenesis through transmitting miR-23a. Knockdown of HIF-1α prevented the increase of exosomal miR-23a while miR-23a inhibited HIF-1α regulators, PHD1, and PHD2 expression and enhanced HIF-1α signaling. Meanwhile, hypoxia-induced exosomal miR-23a could inhibit tight junction protein ZO-1 and increase vascular permeability [71]. Interestingly, exosomal miR-23a upregulation was also observed in chemical-induced hypoxic liver cancer cell colonies established from culturing hepatic cancer cells on the soft agar. Results suggested that exosome-shuttled miR23a was capable of inducing angiogenesis by regulating pro-angiogenic marker genes and targeting SIRT-1 in chick chorioallantoic membrane (CAM), in ovo xenograft, and in HUVEC model system [87]. Umezu et al. established hypoxia-resistant multiple myeloma cell lines under 6 to 7 months hypoxic incubation to better mimic in vivo conditions of hypoxia bone marrow. Exosomal miR-135b derived from those cell lines enhanced endothelial tube formation under hypoxia via the HIF-FIH signaling pathway. Current studies mainly focused on acute hypoxia, which may differ from in vivo conditions. This is the first study that reported exosome-mediated cell-cell communication under chronic hypoxia [94].

Hypoxic exosomal non-coding RNAs can regulate angiogenesis by inducing phenotypic and functional changes in endothelial cells to promote tumor growth and metastasis. VEGFR inhibitors serve as the most vastly applied anti-angiogenesis agents now. They are bringing beneficial efficacies as well as nonnegligible problems like a double-edge sword. Exploiting the anti-angiogenesis potential of RNA therapy via exosomes might be a new therapeutic strategy in the future.