Exosome-Mediated Signaling in Epithelial to Mesenchymal Transition and Tumor Progression.

Growing evidence points to exosomes as key mediators of cell⁻cell communication, by transferring their specific cargo (e.g., proteins, lipids, DNA and RNA molecules) from producing to receiving cells. In cancer, the regulation of the exosome-mediated intercellular communication may be reshaped, inducing relevant changes in gene expression of recipient cells in addition to microenvironment alterations. Notably, exosomes may deliver signals able to induce the transdifferentiation process known as Epithelial-to-Mesenchymal Transition (EMT). In this review, we summarize recent findings on the role of exosomes in tumor progression and EMT, highlighting current knowledge on exosome-mediated intercellular communication in tumor-niche establishment, migration, invasion, and metastasis processes. This body of evidence suggests the relevance of taking into account exosome-mediated signaling and its multifaceted aspects to develop innovative anti-tumoral therapeutic approaches.


Introduction
The lipid-bilayer extracellular vesicles (EVs) include at least three main classes of vesicles that differ in dimension, biogenesis and biophysical properties: exosomes, microvesicles, and apoptotic bodies. Here, we focused on exosomes, small vesicles with an average diameter from 30 to 200 nm that originate inside the Multi Vesicular Bodies (MVBs) and are released by the parental cell after MVB fusion with plasma membrane.
Although exosomes were first identified as garbage disposal [1,2], current knowledge highlights the direct role of these vesicles in governing physiological and pathological conditions by transferring information from producing to receiving cells. Exosomes, indeed, may signal in autocrine but, most importantly, in paracrine and endocrine manner, being taken up by neighboring cells or carried to distant sites. Thus, they assure the horizontal transfer of specific bioactive molecules (including proteins, lipids, RNAs, and DNA [3]) from donor to recipient cells.
Exosomes are ordinarily released by different cell types [4]. They have been identified in various body fluids (including semen, blood, urine, cerebrospinal fluid, and milk) and their role is strongly associated with the cytotype of the producing cells. For example, exosomes participating in supporting immune response [5] and, as vesicles secreted by cells of the nervous system, have been found to coordinate myelin membrane biogenesis, neuronal development, transmission and regeneration [6][7][8]. Interestingly, several studies recently reviewed by Guay and Reguazzi [9], pointed to the involvement of exosomes in a "new endocrinology", being mediators of the crosstalk between metabolic organs. when transferred to the receiving cells, impacting their fate [24]. Nucleic acid analysis revealed, inside exosomes, an abundance of RNA families that, protected from RNases by lipoprotein envelop, maintain their functions. Notably, specific subsets of miRNAs appear to preferentially localize to exosomes [25][26][27] and, as demonstrated by Pegtel at al. [28], exosome-mediated miRNAs delivery directly modulates specific targets once in the cytoplasm of receiving cells. Even if numerically less abundant than small RNAs, long non-coding RNAs (lncRNAs) have been found in exosomes released by different cell types, specifically by tumor cells, thus representing new specific tumor markers [29][30][31]. However, further studies are required to fully understand the effects induced by non-coding RNAs in target cells, specifically concerning lncRNAs, whose pleiotropic roles make them protagonists in the control of gene expression from epigenetics to miRNAs inhibition. Concerning this, two interesting manuscripts from the Lorico group [32,33] demonstrated that internalized exosomes, or part of these, can directly reach the nucleus of receiving cells. These data initiate interest on all of the compounds that, transported by the exosomes, have a nuclear biological activity (e.g., transcription factors, histone modification enzymes, and lncRNAs).
Deeper investigations are required also to characterize the loading of specific macromolecules. The study of miRNA-motifs mediated loading are so far limited to a few reports that identified specific RNA-binding-proteins and some miRNA consensus sequences mediating the process [34][35][36]. While the mechanisms of selective loading of RNAs, as well as proteins, in exosomes are still poorly understood, it is conceivable that pH [37] and hypoxia [38] may affect both the entity of the release and the sorting of a specific content. The lack of standardized well-characterized methods to isolate, purify, and quantify the exosomes further limits the study of their content as cell signature.
The high variability of exosome-induced effects is also determined by the type of interactions occurring between exosomes and target cells that, as recently reviewed in [39], are governed by numerous factors. Depending on their origin, exosomes have been found to interact preferentially with specific cell types, and this interaction seems to be strongly conditioned by the integrins exposed on the exosome surface [40]. It is conceivable that an extensive proteomic analysis of adhesion proteins, such as extracellular matrix proteins (e.g., fibronectin and laminin) and tetraspanins might help to predict exosome-cell interactions but we lack efficient protocols for the isolation of outer membrane proteins only.
Once in touch with target cells, the strategy used to transform these are multiple. First, exosomes may activate receiving cells from the outside, through a ligand/receptor interaction and subsequent activation of downstream pathways.
Paradigmatic is the immune tolerance induced by several cancer cells through exosomes, which express death signals as the PD-L1 (programmed death-ligand 1) or Fas Ligand, and systemically induce apoptosis in receiving T cells and Natural Killer (NK) cells [41,42]. Ligand /receptor interaction have a role also in exosome migration around the body as recently demonstrated for CCR7 (CC-chemokine receptor 7) that, exposed on the Dendritic Cell exosomes, contributes to both their migration on spleen and the induction of inflammation [43]. Exosomes expressing the amphiregulin (AREG), isolated from several tumor cells, have been found able to activate the Epidermal Growth Factor Receptor (EGFR) in receiving cells thus affecting the bone marrow microenvironment [44] or promoting bone metastases [45]. Finally, several groups demonstrated a regulation of the Transforming Growth Factor (TGF)β pathway mediated by membrane-bound molecules [46,47] or (GPI)-anchored cell surface glycoprotein [48].
In most cases, the interaction with cellular receptors drives exosome internalization. Receptors or proteins located on the EV surface participate in fusion, endocytosis or phagocytosis with subsequent release of the exosome content in the receiving cells.

EMT Associated with Tumor Progression: The Role of Exosomes
EMT is a physiological or pathological transdifferentiation process in which epithelial cells lose their cell-cell contacts and apicobasal polarity and acquire mesenchymal properties, coupled to the ability to migrate and to invade the surrounding tissues. EMT is crucial in organogenesis, development, wound healing and regeneration but it is aberrantly activated in tumor progression and metastasis (for review, [49]). EMT, indeed, allows in situ differentiated cells to acquire the ability to migrate out of the primary tumor, invading basement membrane and entering the vasculature. Transitional tumor cells exit from circulation and migrate into the tissue parenchyma in potentially secondary tumor sites. In this process of colonization of target tissues by metastatic cells (as well as during morphogenesis), the shift toward a mesenchymal state is often reversed by an inverse Mesenchymal-to-Epithelial Transition (MET). The MET occurs in different microenvironments and it is necessary to support the reacquisition of epithelial features to seed metastasis [50,51].
Rather than a simple shift between two alternative states (i.e., the mesenchymal and the epithelial phenotype), the current view is that the EMT/MET implies multiple and dynamic transdifferentiation states. This greater flexibility may result in a "partial EMT" or in the co-presence of epithelial and mesenchymal traits, as in the hybrid "metastable" features identified in several tumors [59][60][61] and attributed to a stem phenotype [62][63][64][65]. The complexity of the EMT/MET phenotypes reflects the complexity of the regulatory circuitries that, beyond the transcriptional control, also involve several ncRNAs, including miRNAs (e.g., miR-200 family or miR-34) [66][67][68] or lncRNAs (e.g., HOTAIR) [57]. Notably, transitional tumor cells need to be continuously reprogrammed to adapt to different microenvironments and to ensure tumor growth and metastasis [69][70][71].
Exosome composition profoundly differs between untransformed and transformed cells [72][73][74] and increasing evidence suggests that tumor-derived exosomes (TDEs), as well as exosomes from tumor associated cells in the microenvironment (TME), exert a key role in the regulation of tumor growth and survival as well as tumor invasion, angiogenesis, and metastasis.
It is conceivable that a fine tuning of the EMT plasticity may result in the capacity by the cell to export specific bioactive molecules and, vice versa, the exosome-mediated signaling may impact on the EMT/MET dynamics. Coherently, exosomes from transitional cells exert a role in the regulation of tumor niche, migration, invasion, and metastasis.

Exosomes in Tumor Niche
In primary tumor, exosomes contribute to the definition of tumor niche by promoting tumor growth (despite nutrient deprivation and stress condition), immune suppression and drug resistance, and enhancing vasculogenesis.
Cell growth can be stimulated by cytokines that, loaded in TDEs, are then transported to closer tumor cells; Raimondo et al. demonstrated that exosomes released by chronic myeloid leukemia cells promoted tumor cell growth and inhibited apoptosis by activating TGFβ receptor [46]. Moreover, TDEs can induce proliferation of adjacent cells by non-coding RNA-mediated signaling e.g., the miR-27 in gastric cancer exosomes [81] and the lncRNA c-Myc-Upregulated (MYU) in prostate cancer exosomes [82]. Meanwhile, paracrine stimulation of tumor cell proliferation is induced by cancer associate fibroblasts (CAFs). These cells are pivotal players in the tumor microenvironment by stimulating Cancer Stem Cells maintenance and EMT [83]. Interestingly, exosomes released by tumor cells may activate resident fibroblasts inducing CAFs [81,84]. In bladder cancer, Ringuette et al. showed that CAF activation is mainly due to the induction of TGFβ/Small Mothers Against Decapentaplegic (SMAD) pathway resulting from the transport of TGFβ by TDEs [84]. Furthermore, in gastric cancer an important contribute to fibroblasts activation is due to the exosome mediated transport of miR-27a [81].
The contribution of CAF released exosomes to tumor growth is supported by studies investigating CAF proteome and transcriptome that identified a huge number of molecules with pro tumorigenic activity [85,86]. Interestingly, Zhang and colleagues underlined the possibility that exosomes may carry both pro-and anti-tumor factors. These authors, in fact, by comparing miRNA sequencing of exosomes derived from CAFs and exosomes secreted by fibroblasts from HCC (Hepatocellular Carcinoma) patients, demonstrated that CAF-derived exosomes stimulate cell proliferation lacking protective elements such as the miR-320a that, on the contrary, is transported by NF-exo and is able to inhibit HCC growth through MAPK targeting [87].
TDEs may also contribute to acidification of the tumor microenvironment by modulating stromal cell metabolism. Recently, it was demonstrated that human melanoma-derived exosomes,

Exosomes in Tumor Niche
In primary tumor, exosomes contribute to the definition of tumor niche by promoting tumor growth (despite nutrient deprivation and stress condition), immune suppression and drug resistance, and enhancing vasculogenesis.
Cell growth can be stimulated by cytokines that, loaded in TDEs, are then transported to closer tumor cells; Raimondo et al. demonstrated that exosomes released by chronic myeloid leukemia cells promoted tumor cell growth and inhibited apoptosis by activating TGFβ receptor [46]. Moreover, TDEs can induce proliferation of adjacent cells by non-coding RNA-mediated signaling e.g., the miR-27 in gastric cancer exosomes [81] and the lncRNA c-Myc-Upregulated (MYU) in prostate cancer exosomes [82]. Meanwhile, paracrine stimulation of tumor cell proliferation is induced by cancer associate fibroblasts (CAFs). These cells are pivotal players in the tumor microenvironment by stimulating Cancer Stem Cells maintenance and EMT [83]. Interestingly, exosomes released by tumor cells may activate resident fibroblasts inducing CAFs [81,84]. In bladder cancer, Ringuette et al. showed that CAF activation is mainly due to the induction of TGFβ/Small Mothers Against Decapentaplegic (SMAD) pathway resulting from the transport of TGFβ by TDEs [84]. Furthermore, in gastric cancer an important contribute to fibroblasts activation is due to the exosome mediated transport of miR-27a [81].
The contribution of CAF released exosomes to tumor growth is supported by studies investigating CAF proteome and transcriptome that identified a huge number of molecules with pro tumorigenic activity [85,86]. Interestingly, Zhang and colleagues underlined the possibility that exosomes may carry both pro-and anti-tumor factors. These authors, in fact, by comparing miRNA sequencing of exosomes derived from CAFs and exosomes secreted by fibroblasts from HCC (Hepatocellular Carcinoma) patients, demonstrated that CAF-derived exosomes stimulate cell proliferation lacking protective elements such as the miR-320a that, on the contrary, is transported by NF-exo and is able to inhibit HCC growth through MAPK targeting [87].
TDEs may also contribute to acidification of the tumor microenvironment by modulating stromal cell metabolism. Recently, it was demonstrated that human melanoma-derived exosomes, once internalized by dermal fibroblasts, promote aerobic glycolysis and downregulate oxidative phosphorylation [88]. Meanwhile, the Nagrath group elegantly demonstrated that exosomes from CAFs downregulate mitochondrial activity and increase glycolysis. Furthermore, intra-exosome metabolomic analyses showed that exosomes contain metabolites, amino acids, and lipids, "which can fuel the metabolic activity of the recipient cells" [89].
Finally, as mentioned above, exosomes indirectly support tumor growth by favoring immune escape in different ways; they inactivate T cells or induce their apoptosis by cell surface interaction or after internalization [90][91][92]. With respect to immunomodulatory properties, TDEs exposing CD39 and CD37 on their surface can mediate T-cell suppression by extracellular adenosine production [93]. Meanwhile it was shown that the internalization by Kupffer cells of pancreatic ductal adenocarcinoma TDEs induced fibronectin production, thus promoting the gathering of bone marrow-derived macrophages and neutrophils and leading to liver pre-metastatic niche formation [94].
A key component of tumor microenvironment is the vascular network that supports tumor growth; several extracellular mechanisms take part in endothelial cell stimulation, among these TDEs contribute to modulating both angiogenesis and vascular permeability [95].
It is of note that the ability to promote angiogenesis has been mainly attributed to exosomes isolated from tumor initiating cells (TICs). In renal cell carcinoma and hepatocellular carcinoma for example, only CD105+ and CD90+ cells respectively, release exosomes able to stimulate production and release of the Vascular Endothelial Growth Factor (VEGF); TIC derived exosomes, once engulfed in endothelial cells, activate the VEGF autocrine loop through the delivery of different ncRNAs [31,96]. Recently, Sun et al. demonstrated pro-angiogenetic activity also in exosomes from Glioma stem cells, that stimulate endothelial cell motility by activating a miR-21/VEGF/Vascular Endothelial Growth Factor Receptor (VEGFR) 2 signal pathway [97]. In addition, exosomes can directly stimulate endothelial cell VEGF receptor through the delivery of 90-kDa VEGF (VEGF90k), which was found to interact with Hsp90 in extracellular vesicles [98].
Several observations correlate hypoxia, exosomes, and neo angiogenesis stimulation. Low oxygen partial pressure, a common characteristic of all types of cancer, induces activation and nuclear translocation of the transcription factor HIF1 that, inside the nucleus, interacts with several co-factors to induce the up regulation of a huge number of genes whose coordinated expression drives tumor cells to a most aggressive phenotype [99]. Among the HIF target is the VEGF. Evidence collected in past years demonstrated that hypoxia stimulates production and release of exosomes [100] that, in turn participate in promotion of tumor neo-angiogenesis as described by ref. [101] and enclosed references.
Although VEGF signaling is the best-validated pathway in angiogenesis, the refractoriness to anti-VEGF therapies in several cancers highlighted the involvement of VEGF-independent strategies in promoting tumor angiogenesis [102]. An interesting study performed by Tang et al. [103] demonstrated that exosomes, released by ovarian cancer cells, participate in cleavage and delivery of soluble E-cadherin that once delivered on endothelial cell surface, interacts with VE-cadherin and induces activation of β-catenin and Nuclear Factor kappa-light-chain-enhancer of activated B cells (NF-κB) signaling, resulting in endothelial cell migration, and tube formation in vitro and in vivo.

Exosomes in Migration, Invasion, and Metastasis
A body of evidence points to the role of exosome-triggered EMT in the inception of high metastatic potential that correlates with high motility and increased invasiveness. Exosomes from cancer cells were found to be able to activate intracellular pathways by transporting specific proteins such as phosphorylated tyrosine kinases receptor (RTKs) [104]. Exosomes from muscle-invasive bladder cancer induced a decrease in E-cadherin expression and enhanced migration and invasion of uroepithelial cells [79]. Similarly, exosomes from highly metastatic lung cancer cells induced an EMT associated with migration, invasion, and proliferation in recipient human bronchial epithelial cells [105]. Furthermore, exosomes secreted by highly metastatic MHCC97H hepatocarcinoma (HCC) cells conferred the ability to migrate and give invasiveness properties to low metastatic HCC cells by inducing EMT via MAPK/Extracellular signal-Regulated Kinase (ERK) signaling pathway activation [106]. Finally, human breast and colorectal cancer cells released full-length, signaling-competent EGFR ligands, i.e., amphiregulin, able to increase the invasiveness of recipient cancer cells [107].
Harris et al. investigated the role of exosomes released from different breast cancer cells, modeling different stages of metastasis. They showed that tumor cells of increasing metastatic potential are able to secrete exosomes with protein signatures different in identity and abundance; these exosomes increased cell migration proportionally, with exosomes from high-metastatic potential cells able to induce the greatest degree of cell movement [108]. Interestingly, xenograft tumor cell motility studies in the chorioallantoic membrane (CAM) of chick embryos revealed a key role of exosome secretion for the directional migration of fibrosarcoma cells. These vesicles, indeed, carry extracellular matrix (ECM) molecules promoting adhesion assembly [109].
Furthermore, Schillaci et al. [110] recently demonstrated that exosomes released by metastatic colon cancer cell lines affected tumor behavior promoting a more aggressive phenotype. They found that metastatic amoeboid cells (SW620) release exosomes that are enriched in Thrombin, activating RhoA/Rho-associated protein kinase (ROCK) pathway in receiving cells. This activation induces migration and invasion in primary tumor cells while, in endothelial cells, causes VE-cadherin delocalization and junction disruption.
Concerning exosomal lncRNAs, a role for BCAR4 (breast cancer anti-estrogen resistance 4) has been suggested in colorectal cancer development [111] while HOTAIR (Hox antisense intergenic RNA) was found overexpressed in bladder cancer patients and correlated with the invasiveness of the tumor [30]. Notably, HOTAIR has a key functional role in promoting EMT in different cell types [57,112,113].
With respect to TMEs, Luga et al. demonstrated that CD81-positive CAF-released exosomes induced in breast cancer cells the release of Wnt11 that, in an autocrine manner, promoted the activation of Planar Cell Polarity (PCP) [114]. Meanwhile, Condorelli's group attributed the induction of EMT in breast cancer to three different miRNAs (miRs-21, -378e, and -143), delivered by CAF-derived exosomes [115]. These observations enforced the idea that cellular transformation, induced by exosome uptake, must be mediated by multiple biological compounds that converge on the same molecular pathways. Li and collaborators demonstrated that ovarian CAF-derived exosomes were enriched in TGFβ1 that may induce an EMT and an aggressive phenotype in ovarian cancer cells lines [116]. More recently, Zhao and colleagues demonstrated that human umbilical cord mesenchymal stem cells-derived conditioned medium was able to induce migration and invasion capability in A549 lung cancer cells by activating TGFβ-related pathways [117].
The ability to migrate and invade surrounding tissues can be enhanced by hypoxia-induced exosomes by shuttling different molecules. Firstly, exosomes released in hypoxia may contain hypoxia-inducible factors (HIFs), able to trigger EMT in recipient cells [78]. Coherently, Ramteke and colleagues showed that hypoxia-induced exosomes increased the invasiveness of prostate cancer cells by promoting the loss of E-cadherin [118]. Furthermore, exosome-mediated mechanisms to promote migration and invasiveness by tumor cells in hypoxia may involve lncRNAs, such as UCA1 in bladder cancer cells [119] or the lncRNA-regulator of reprogramming (RoR) in HCC [120], as well as specific miRNAs, e.g., miR-21 in oral squamous cell carcinoma [94] or miR-23a in lung cancer [121].
Interestingly, Zhou and colleagues reported that exosomes secreted by cervical squamous cell carcinoma (CSCC) cells may shuttle miR-221-3p, targeting vasohibin1 (VASH1), to human lymphatic endothelial cells (HLECs). This promotes migration in vitro as well as lymphangiogenesis and lymph node metastasis in vivo [122].
The role of TDEs is not limited to the primary tumor site and their ability to cross long distances within the body makes exosomes a suitable vehicle to trace the way of tumor metastases. TDEs promote the organotropism of metastatic tumors and contribute to pre-metastatic niche formation by showing "avidity" for specific recipient cells [11,40,94]. Notably, Hoshino and colleagues showed that the exosomal integrins guide the exosomes to specific secondary sites. Furthermore, exosomes from lung-, liver-and brain-tropic tumor cells preferentially fuse with lung fibroblasts and epithelial cells, liver Kupffer cells, and brain endothelial cells [40].

Conclusions and Perspectives
EMT exerts a key role in tumor progression and exosomes, released by transitional cells, transport specific signaling molecules to promote invasion, migration, metastasis, and microenvironment changes, able to sustain tumor growth and dissemination. In fact, the horizontally transferred TDE specific content promotes the acquisition by tumor cells of mesenchymal markers and increases cell motility, associated with a more aggressive phenotype. Furthermore, exosome cargo impacts on tumor niche establishment and regulates the tropism of metastasis (Tables 1 and 2). Therefore, the identification of molecules (mRNA, ncRNAs, proteins) specifically enriched in exosomes from different tumor stages may represent an efficient real-time staging of tumor evolution or response to therapy, also in patients differing in gender or age. Notably, EVs may be isolated from body fluids, and several RNA and protein molecules have already been identified as potential diagnostic and prognostic biomarkers of different tumor types or different stages of the same tumor. Interestingly, the study of the secretome of HCC cells overexpressing the master transcriptional factor Slug, and exhibiting a partial EMT phenotype, showed the enrichment in exosomes of Fibronectin 1 (FN1), collagen type II alpha 1 (COL2A1), and fibrinogen gamma chain (FGG); therefore, these proteins may represent useful and non-invasive biomarkers associated with partial transitional cells [123]. Notably, a partial EMT may characterize circulating tumor cells (CTCs) that pose a metastatic risk for patients [124]. Table 1. Summary of recent evidence on exosome signaling molecules and their effects on tumor progression.

Bladder cancer cells Colon cancer cell lines
RhoA/ROCK (Rho-associated protein kinase) signaling pathway activation and acquisition of migratory capacity [79,110] Epstein-Barr-Virus EBV infected Nasopharyngeal carcinoma (NPC) HIF1 upregulation [78] metastatic melanoma cells MET induced pro-vasculogenic and metastatic effects [11] Hypoxic cancer cells Activation of Epithelial-to-Mesenchymal Transition (EMT) genes in receiving cells [101] and enclosed references Lung cancer cells vimentin [105] Hepatocellular carcinoma cells MAPK/ERK (Extracellular signal-Regulated Kinase) signalling activation (unknown mechanism) [106] High aggressive breast cancer proteins involved in metastasis and invasion [108] Prostate cancer cells metalloproteinases induction and targeting of adherens junction proteins [118] Hypoxic bladder cancer lncRNA-UCA1 (Urothelial Cancer Associated 1) (mechanism of action unspecified) [119] Metastatic breast cancer miR-10b targeting HOXD10 (HomeoboxD10) [126]  CAF from Hepatocellular carcinoma MAPK activation [87] CAF from breast cancer EMT activation by miRs -21, miR-378 and miR-143 [115] CAF from ovarian cancer TGF (Transforming Growth Factor) β1-induced EMT [116] Mesenchymal stem cells  CAF from breast cancer miR-21, miR-378e and mir-143-mediated Cancer Stem Cells maintenance [113] Renal cell carcinoma lncRNA ARSR-mediated chemoresistance via competitively binding of miR-34/miR-449. [128] Metabolism modulation Melanoma cells miR-155 and miR-210-mediated promotion of glycolysis and inhibition of oxidative phosphorylation. [88] CAF from prostate cancer and from pancreatic cancer Metabolites inhibiting mitochondrial oxidative phosphorylation and increasing glycolysis. [89] All further efforts in the study of biomarkers would have a great impact particularly on early diagnosis, considering that the development of non-invasive diagnostic tools currently represents a major challenge. Moreover, an optimization of exosome isolation protocols is required to better disclose the functional role of specific exosome cargo molecules. The isolation of exosomes with high purity and quality is still difficult and the demonstrated heterogeneity of exosomes further impairs the isolation efficiency; all these aspects represent a limitation, particularly for the study of low copy number molecule species, such as lncRNAs.
A deep understanding of mechanisms controlling the loading of specific molecules in exosomes is also needed. This field of study is to be considered still at infancy even if some mechanisms of sequence-specific miRNA sorting (by EXO-and hEXO-motifs) and specific heterogeneous nuclear ribonucleoproteins (hnRNPA2B1 and hnRNPQ) involved in the recognition of these signals, have been recently identified [34,35]. Interestingly, the sorting of lncRNA ARSR in exosomes by renal cancer cells also involves hnRNPA2B1 [128]; furthermore, a "zipcode" in the mRNAs may control their selective loading [129]. All of this evidence suggests common regulative mechanisms, at least for RNA loading, and opens the way towards possible innovative therapeutic strategies oriented to the selective modulation of RNA exosomal cargo by engineering signaling sequences. Other approaches could aim to interfere with, or promote, the in vivo sorting of these vesicles. The use of specific inhibitors, targeting key regulators of both exosome biogenesis and release, could be a suitable approach. For example, the release of EVs by primary hepatocytes and Huh7 cells may be reduced by inactivating mediators of the DR5 signaling pathway or ROCK1 inhibition. Interestingly, the ROCK1 inhibitor fasudil reduced serum levels of EVs in nonalcoholic steatohepatitis (NASH) mice and this reduction was associated with decreased liver injury, inflammation, and fibrosis [130]. The drug GW4869 was efficiently used to inhibit exosome biogenesis by interfering with sphingomyelinase function [125,126]. The release of exosomes was shown to be influenced by calcium and the monensin drug was found able to affect exosome biogenesis [131]. Further studies are still necessary to investigate the effective translational application of these protocols.
Remarkably, exosomes show low immunogenicity, high biocompatibility, and high efficacy of delivery. Considering all these features, they might be engineered to convey molecules of interest and achieve targeted therapeutic intervention. For a recent example, paclitaxel-loaded exosomes, modified to improve circulation time, were shown to selectively deliver the drug to target cancer cells and increase the survival rate of lung cancer patients [132].
Finally, an in-depth understanding of exosome cargo composition and functional role in EMT associated with tumor progression would pave the way for innovative therapeutic opportunities. In particular, further studies must be focused on the characterization and potential engineering in vivo and/or ex vivo of exosomes from EMT cells. The plasticity of transitional cells might, indeed, imply a fine-tuning regulation of the loading machinery that, in turn, might be mirrored by the great complexity of exosome cargoes.
Author Contributions: Both authors made substantial contributions to the conception and design of the work and approved the submitted version (Conceptualization, A.C. and C.C.; Writing-Original Draft Preparation, Review and Editing, A.C. and C.C.; Funding Acquisition, A.C. and C.C.).