Exosomes: A Promising Avenue for the Diagnosis of Breast Cancer.

Currently, despite the advances in individualized treatment, breast cancer still remains the deadliest form of cancer in women. Diagnostic, prognostic, and therapy-predictive methods are mainly based on the evaluation of tumor tissue samples and are aimed to improve the overall therapeutic level. Therefore, the exploration of a series of circulating biomarkers, which serve as the information source of tumors and could be obtained by peripheral blood samples, represents a high field of interest. Apart from classical biomarkers, exosomes, which are nanovesicles, are emerging as an accessible and efficient source of cell information. The purpose of this review is to summarize the peculiarities of the presently available breast cancer exosomal biomarkers; the review also provides the prediction of a multitude of potential target genes of exosomal microRNAs using 4 databases.

Introduction

Breast cancer (BrCa) remains the most prevalent type of cancer occurring in women worldwide, with no less than 1 000 000 new cases diagnosed each year.[1] Although the prognosis of patients with BrCa has improved substantially, approximately one-third of women still die from this disease, mainly from metastasis, especially in the brain.[2-4] With the rapid development of modern clinical medicine, early diagnosis of BrCa is crucial to enhance therapeutic outcomes and survivor rate. Mammography is widely used for BrCa screening,[5] but it is limited due to the minimum detectable tumor size and the low radiation utilized on some patients.[6] Liquid detection, because of its nondestructiveness and low cost, is emerging as a novel method of BrCa diagnosis. Molecular biomarkers, such as the progesterone receptor, estrogen receptor (ER), and human epidermal growth factor receptor (Her2/ErBb2), are used for diagnosis or for predicting outcomes.[7,8] However, these biomarkers are not sufficient or reliable to timely screen tumor cells extracted from the peripheral blood of patients with BrCa. Hence, it is imperative to determine more precise biomarkers for diagnosing cancer at an early stage.

Exosomes, secreted by all viable cells, are nanovesicles of approximately 30 to 100 nm in diameter that are produced in the endosomal pathway and play a vital role in paracrine and autocrine cell communication.[9] They carry a broad repertoire of cargo, such as proteins, lipids, messenger RNAs (mRNAs), microRNAs (miRNAs), long-noncoding RNA (lncRNA), and DNA.[10,11] Furthermore, exosomes broadly exist in physiological or pathological fluids, including plasma, serum, saliva, urine, breast milk, cerebrospinal fluid, and ascites.[12] As reported, tumor cells may release more exosomes than normal cells, with a certain number of cancer-specific biomarkers. As they are easily accessible and maintain stability in vitro, exosomes have been regarded as the most promising and fundamental indicators[13] for the early diagnosis of patients or for predicting outcomes after different types of treatments with targeting molecules, such as heat shock proteins,[14] survivin,[15] and miR-221/222.[16] These proteins and miRs exist extensively in exosomes and are closely related to the development and metastasis of BrCa.[17-19] Indeed, approximately 270 articles on “exosome and BrCa” are found in the PubMed database, most of which were published within the last 5 years. Dissemination of the current knowledge to a broader range of scientific groups or clinical staff can aid in the understanding and utilization of these fascinating nanoparticles. Hence, in this review, we summarize the current knowledge of the diagnostic applications of exosomes in BrCa.

The Biological Activity of Exosomes

Initially, extracellular vehicles (EVs) were discovered by Siekevitz[20] as cellular debris after cell damage. In contrast to the prime hypothesis, EVs may contain numerous surface components and cytoplasmic molecules, which originate from their host cells. Although the molecular mechanisms promoting cell-to-cell communication are not fully understood, recent studies have shown that EVs may participate in transferring specific proteins and nucleic acids to recipient cells.[21] Exosomes are one kind of cell-derived EVs, with a size of 30 to 120 nm in diameter. The profiles of exosome sare presented in Figure 1. The biological functions of exosomes include antigen presentation, immune regulation, evading apoptosis, drug resistance, and escape from immune surveillance.[22,23] As a communication tool, exosomes derived from cancer cells have the potential to transfer a malignant phenotype to normal cells and establish a fertile local and distant microenvironment. As a result, exosomes could be used as a source for biomarkers for predicting metastatic spread, targeted drug delivery, cell free antitumor vaccination, and gene therapy.[24,25] In addition, the latest reports have proven that exosomes often correlate with an increase in blood vessel thrombosis by transporting the pro-coagulant receptor, tissue factor (TF).[26,27] Fausto[28] and colleagues reported that BrCa cell-derived exosomes may induce TF-independent platelet activation and aggregation, as well as TF-dependent plasma clotting and platelet aggregation, by means of thrombin generation.

Figure 1.

Schematic Representation of exosomes. The structure and contents of exosomes are demonstrated in this plot. The lipid bilayer membrane of exosomes, sharing similar topology to the original cells, carries typical transmembrane proteins and receptors. In addition, the contents of exosomes can be transferred from the original cell to their target cell, including RNA species (mRNAs, miRNAs, and other types of short RNAs) and a vast array of different proteins.

Implications for BrCa Diagnosis

Survival of patients with BrCa depends on the stage at diagnosis, with patients in whom the disease is detected earlier having more favorable outcomes.[29] Hence, numerous scientific groups are concentrating on the development of a more efficient and accurate biomarker for BrCa. Apart from classical markers, exosomes are becoming a very accessible source, with extensive information about tumor biological characteristics (proteins and nucleic acids) gathered from liquid biopsy.[30] The process of exosome utilization in BrCa diagnosis is shown in Figure 2, which illustrates the use of exosomes in diagnostic and therapeutic applications.

Figure 2.

Exosome application in BrCa diagnosis. This plot demonstrates the process of utilizing exosomes in BrCa diagnosis.

Exosomal Protein in BrCa Diagnosis

Proteins, which are part of the molecular content in exosomes, are heavily dependent on cellular origin. Exosomes possess a series of conservative proteins across species, suggesting valuable, even life-preserving functions.[31] For example, almost all exosomes contain cytoplasmic proteins, such as tubulin,[32] actin-binding proteins, annexins,[33] and Rab proteins,[34] such as signal transduction proteins-kinases and heterotrimeric G-proteins.[35] Many exosomes also contain heat-shock proteins (Hsp)70 and Hsp90[14] and major histocompatibility complex class I molecules.[36] Except for a series of normal proteins, the function of exosomes seems to be controlled by cell-specific proteins that reveal the distinctive function of their source cells, such as tumor antigens (gp100, CEA, and Her2)[37-39] or death receptors (FasL and TRAIL).[40,41] Here, we report the potential functions of exosomes present in BrCa cells that can serve as putative common markers at the early stage. lists a detailed brief overview of known BrCa cell-derived exosomal proteins reported by various scientists.

Table 1.

The Exosomal Proteins in Breast Cancer (1).

Exosomal Protein	Body Fluid	Isolation/Detection Method	Application	Ref.
Metalloprotease ADAM10, tetraspanin CD9, HSP 70 and Annexin-1	Breast cancer cell line culture supernatants, serum, pleural effusions	Western blot	Identification and highly expressed on breast cancer cell derived exosomes	Hernandez et al [42]
CD24, tetraspanins and epithelial cell adhesion molecule (EpCam)	Serum, ascites fluid	Ultracentrifugation and sucrose gradient/MACs using beads	Early diagnosis	Rupp et al [43]
Developmental endothelial locus-1 (Del-1)	Plasma	ELISA	Diagnosis/monitoring	Moon et al [44]
Fibronectin	Plasma	ELISA	Early diagnosis	Moon et al [45]
Survivin (Survivn 2B)	Serum	ExoQuick and ELISA	Diagnosis/prognosis	Khan et al.,[15]
HER-2	Serum, breast cancer cell line culture supernatants	Ultracentrifugation and Bradford assay	Trastuzumab Resistance and tumor aggressiveness	Ciravolo et al [46]
Annexin A2	Breast cancer cell line culture supernatants	Atomic force microscopy and Western blot	Brain and lung metastasis	Maji et al [47]
P-glycoprotein/TrpC5/ABCG2	MCF-7/S cell culture supernatants	Binding of exosomes to nonmalignant cells	Mlutidrug resistance	Jaiswal et al,[48] Matula et al,[49] and Ma et al [50]
Glutathione S-transferase P1(GSTP-1)	Cell, tissue, and serum	Cell apoptosis and immunofluorescence staining assays	Adriamycin-resistant	Yang et al [51]
Ubiquitin carboxyl terminal hydrolase-L1	MCF-7 cell culture supernatants	Western blot and immunohistochemistry	Adriamycin resistance	Ning et al [52]

ELISA, enzyme-linked immunosorbent assay.

Evidence from numerous experiments has shown that some of the tumor markers detected in the blood of patients with BrCa are carried by membrane vesicles[53]; this implies that biomarker research can also benefit from vesicle characterization. Recently, proteomic analysis has become the technique of choice for characterizing exosomes, as a wider knowledge of exosomal protein content can help in understanding the potential roles of exosomes in vivo and in identifying new tumoral markers with diagnostic value.[54]

Rupp and colleagues[43] suggested that both CD24 and EpCAM from ascites and pleural effusions can serve as alternative BrCa-derived exosome markers; these were isolated using magnetic beads and detected by Western blot. Further, in the serum of patients with BrCa, CD24 alone could be detected in the exosomes, but EpCAM was lost; this indicated that exosomal CD24 may serve as a circulating BrCa biomarker. However, CD24 has been implicated in numerous cancer types, including colorectal cancer (CC), so it may serve as a general cancer marker and not a specific BrCa marker.[55]

BrCa Exosomal Protein as an Early Diagnostic and/or Prognostic Marker

Several exosomal proteins are differentially expressed in certain stages or types of BrCa and may be applied as diagnostic or prognostic markers for general cancer diagnosis. For instance, metalloprotease ADAM10, in addition to tetraspanin CD9, HSP70, and Annexin-1, was specifically expressed in serum/pleural effusion-derived exosomes from patients with BrCa or BrCa cell lines.[42] Furthermore, the tetraspanin CD63, a binding partner of integrins and a tumor marker whose expression conversely correlates with cancer metastasis,[56-62] and tumor susceptibility gene 101, which is a subunit of the endosomal sorting complex required for transport-1 (ESCRT-1),[63] existed exclusively on exosomes.[64]

Moon and colleagues[44,45] have demonstrated that both developmental endothelial Locus-1 (Del-1) and fibronectin on circulating exosomes from the plasma of patients with BrCa could serve as promising biomarkers at the early stage. In addition, Del-1 is also a promising marker to distinguish BrCa from benign breast tumors and noncancerous disease. Khan et al [15] found that the differential expression of exosomal Survivin-2B (proapoptotic protein) in the sera may be used as a diagnostic and/or prognostic marker in patients with early BrCa.

Breast Cancer Metastasis

Currently, the terms “metastatic niche” and “premetastatic niche” are widely accepted to describe regulation at secondary organs at distant sites before cancer cells arrive.[65] Tumor cell-derived exosomes, as new critical components of metastasis and premetastatic niches, are able to promote survival and growth of the primary tumor.[66] Afterward, they participate in communication with neighboring nontumor cells[67] by regulating epithelial to mesenchymal transition,[68] inducing local tumor invasion,[69] impacting the immune system,[70] promoting tumor vascular leakiness and facilitating circulating tumor cell access to distant sites,[71,72] which accelerates the progression of the primary tumor. Furthermore, recent discoveries also proved that proteins in exosomes from BrCa cells can promote angiogenesis and organ-specific metastasis. When detected in exosomes, these proteins may imply the presence of tumor metastasis. Maji et al found that Annexin A2(Anx A2)[47] in BrCa cell-derived exosomes is an emerging mediator of brain and lung-specific metastasis. Upon delineating the mechanism, it was found that exo-Anx A2 causes macrophage-mediated activation of the p38MAPK, nuclear factor kappa B, and STAT3 pathways and improved secretion of interleukin (IL)′-6 and tumor necrosis factor-α. In addition, Piao[73] and colleagues have proven that proliferation of BrCa cell-derived exosomes could create a favorable condition for LN metastatic by stimulating macrophage polarization.

Multidrug Resistance in Exosomal Protein

According to reports, antigens presented in the BrCa exosomes may serve as targets for certain therapeutic antibodies and induce treatment failure by capturing the drugs. Ciravolo and colleagues[46] found that exosomes extracted from HER2+ BrCa cell supernatants or the serum of patients with BrCa could bind to trastuzumab. Functional detection revealed that only xenogeneic and autologous HER2+ nanovesicles, but not HER2− ones, inhibited trastuzumab activity in SKBR3 cell proliferation. These findings suggested that HER2-positive exosomes could be a biomarker to indicate trastuzumab resistance and tumor aggressiveness. There are various clinical trials studying circulating HER2 levels as a potential predictor of the trastuzumab response, both as an initial indicator of drug response and as patients progress while on the drug. There was even an Food and Drug Administration-approved HER2 ELISA test developed, which would measure both exo-HER2 and solubilized forms in the extracellular domain. After thorough testing, it was shown that circulating HER2 is not informative, and this product is not used for clinical care.[74]

The overexpression of P-glycoprotein (P-gp) is associated with the multidrug resistance bioprocess.[48] A recent study demonstrated that docetaxel-resistant BrCa cell-derived exosomes transferred P-gp to anticancer drug-sensitive tumor cells; this process is called tunneling nanotube-mediated transportation.[49] The sequential research by Ma’s group[50] revealed that transient receptor potential channel 5 (TrpC5) in exosomes may be responsible for the acquisition and formation of drug resistance in BrCa cells. At the same time, this transfer upregulates the expression of TrpC5 in recipient cells, thereby increasing the quantities of the drug efflux transporter P-gp by a Ca2+ and transcription factor nuclear factor of activated T-cell isoform c3 (NFATc3)-mediated mechanism.[75,76] Currently, a novel multidrug efflux transporter, ATP-binding cassette subfamily G member 2 (ABCG2), is also related to drug resistance, including resistance to mitoxantrone and camptothecin analogs.[77]

Glutathione S-transferase P1 (GSTP1), a member of the phase II metabolic enzyme family, has been shown to function in detoxifying several anticancer drugs by conjugating them with glutathione. Yang et al [51] have analyzed the exosomal GSTP1 expression in BrCa cells and tissues by apoptosis assays and immunofluorescence staining techniques. Higher GSTP1 expression was observed in the serum of adriamycin-resistant cells and a progressive disease/stable disease group. This study proved for the first time that GSTP1-rich exosomes have the capability to transfer drug resistance and therefore could be helpful in predicting chemoresistance in clinical use.

Adriamycin-resistant human BrCa cells (MCF7/ADM) secrete exosomes carrying UCH-L1 and P-gp proteins into the extracellular microenvironment and are then integrated into adriamycin-sensitive human BrCa cells (MCF7/WT) in a time-dependent manner, thereby transferring the chemoresistance phenotype. Kuan Ning et al [52] have demonstrated that UCH-L1-containing exosomes can transfer chemoresistance to recipient cells, and these exosomes may be useful as noninvasive diagnostic biomarkers for the detection of chemoresistance in BrCa patients, thus achieving more effective and individualized chemotherapy. In conclusion, noninvasive detection of specific exosomal proteins may contribute to the development of new strategies in clinical applications for physicians.

Exosomal miRNA in BrCa Diagnosis

The microRNAs present in BrCa exosomes can serve as a novel ideal biomarker, and their expression pattern is correlated with the degree of tumor malignancy[78-81] ( ). Lee’s group[82] used a nanosized oligonucleotide probe, molecular beacon (MB), to carry out in situ miRNA examination. The results further showed that exosomal miR-21 could be used as a biomarker when compared with MCF-7 exosomes and normal cell-derived exosomes. However, miR-21 as a potential biomarker was widely reported and may not only exist in the exosomes of BrCa.[83] Other reports have disclosed that exosomal miR-21 exists in the serum, cerebrospinal fluid, cervicovaginal lavage specimens and peritoneal lavage fluid of CC,[93] gastric cancer,[94] ovarian cancer,[95] pancreatic adenocarcinoma (PC),[96] cervical cancer,[97] and glioblastoma patients.[98]

Table 2.

The Exosomal miRNAs and lncRNA in Breast Cancer(1).

Exosomal RNA	Body Fluid	Isolation/Detection Method	Application	Ref.
miR-21	Plasma/MCF-7 cell culture supernatants	In situ nano-sized oligonucleotide probe	Diagnosis	Lee et al,[82] and Shi et al [83]
miR-101, miR-372	Serum	Quantitative TaqMan MicroRNA assays and correlated with clinicopathological risk factors	Diagnosis	Eichelser et al [84]
miR-373	Serum	Quantitative TaqMan microRNA assays and correlated with clinicopathological risk factors	Diagnosis of Triple-negative breast cancer	Eichelser et al [84]
miR-1246	Plasma andMDA-MB-231 cells	RT-qPCR	Diagnosis	Hannafon et al,[85] and Li et al [86]
miR-105	MCF-10A and MDA-MB-231 cell culture supernatants	RT-qPCR, western blot analysis, and immunofluorescence	Diagnosis	Zhou et al [87]
miR-10b	MDA-MB-231 cell culture supernatants	RT-qPCR	Cell invasion	Singh et al [88]
miR-338-3p, miR-340-5p, miR-124-3p, miR-29b-3p, miR-20b-5p, miR-17-5p, miR-130a-3p, miR-18a-5p, miR-195-5p, miR-486-5p and miR-93-5p	Human serum and tissues	miRNA PCR array	Prognostic	Aiko et al [89]
miR-222/miR-221	MCF-7 cell culture supernatants	Fluorescence in situ hybridization	Adriamycin-resistant	Yu et al [16]
miR-451	MCF-7 cell culture supernatants	Cell apoptosis and in situ nano-sized oligonucleotide probe	Increase the sensitivity of cell resistance to doxorubicin	Chen et al [90]
lncRNA GAS5	MCF-7 and MDA-MB-231 cell culture supernatants	RT-qPCR	Marker of apoptosis induction	Oguz et al [91]
lncRNA MALAT1	Human specimens and cell lines (MCF-7, MDA-MB-231, and MDA-MB-435 S)	qRT-PCR	Promoted cell proliferation	Zhang et al [92]

Abbreviation: RT-qPCR, real-time quantitative polymerase chain reaction.

Breast Cancer Exosomal miRNA as a Biomarker

Eichelser et al [84] reported that BrCa-specific miRNAs are expressed in the serum exosomes of patients. They found that the level of exosomal miR-101 and miR-372 was significantly higher in the serum of patients with BrCa than in healthy controls; furthermore, the level of exosomal miR-373 was more elevated in triple-negative patients than in patients with luminal cancers or healthy controls. All the data indicate that exosomal miR-101 and miR-372 could be used as BrCa biomarkers, while exosomal miR-373 is indicative of a triple-negative phenotype.

Hannafon et al [85] showed that certain miRNA species, such as miR-21 and miR-1246, are ubiquitous in human exosomes and are distinctively elevated in patients with BrCa. Furthermore, their results support the concept that circulating exosome microRNA profiles can be used as an important diagnostic tool for BrCa, and the potential mechanism was further discovered by Li et al.[86] The exosomal miR-1246 could suppress the expression level of Cyclin-G2 , indicating BrCa progression. In addition, exosome-encapsulated miRNAs could serve as a prognostic marker for metastatic progression in BrCa. Zhou et al [87] demonstrated that the level of serum exosomal miR-105 in BrCa-bearing animals increased swiftly in the premetastatic and metastatic stages; this implies that exosomal miR-105 has the potential to predict or diagnose BrCa when metastasis is developing or has already developed. Additionally, the level of exosomal miRNA-10b[88] was higher in TNBC MDA-MB-231 cells, and cell invasion with the noninvasive mammary epithelial cell line HMLE was increased when MDA-MB-231-derived exosomal miRNA-10b was applied to the HMLE cells. In addition, Zhang etal[99] have proven that miR19a is transferred via exosomes from astrocytes to mouse and human BrCa cells and mediates adaptive loss of tumor suppressor PTEN in brain metastatic tumor cells.

Recently, Aiko Sueta[89] and his group detected 384 miRNAs derived from the exosomes of patients with BrCa and demonstrated that miR-338-3p, miR-340-5p, and miR124-3p were obviously upregulated and miR-29b-3p, miR-20b-5p, miR17-5p, miR-130a-3p, miR-18a-5p, miR-195-5p, miR-486-5p, and miR-93-5p were downregulated rapidly in the recrudescent patients. They provided evidence that these 11 exosomal miRNAs are correlated with BrCa recurrence and may be used as prognostic factors for BrCa prognosis. Several limitations existed in their study, including that there was no reliable endogenous gene for normalization, the period of storage for patient samples was not clear, and they utilized ExoQuick (System Biosciences, Palo Alto, CA, USA) to extract exosomes, which may mix nonexosomal contents with similar size. All of these limitations may cause differences in the miRNA expression pattern between exosomes and tumor tissues.

Multidrug Resistance in Exosomal miRNA

Presently, drug resistance still hinders the treatment of BrCa, causing BrCa to become one of the major deadly cancers in women. It is increasingly reported that exosomal miRNA (including miR-100, miR-222, and miR-30a)[100] secreted by drug-resistant BrCa cells may participate in BrCa drug resistance by spreading resistance capacity and altering chemosusceptibility in recipient sensitive cells.

Tamoxifen resistance remains a daunting challenge to the successful treatment of ER+ BrCa. Yu and colleagues[16] proved that exosomal miR-221/222 secreted from tamoxifen-resistant BrCa cells could downregulate its target genes of P27 and ERα proteins, which significantly stimulated drug-resistant cell proliferation and colony-forming ability in the presence of tamoxifen. Chen and colleagues[90] showed that the disproportionately exported exosomal miRNA-451 from BrCa cells could integrate with mdr1 and downregulate the level of P-gp, leading to lower sensitivity to doxorubicin and poor treatment results.

The Potential Research Strategy of Exosomal miRNAs

MiRNAs (miRs) are a major class of small noncoding RNAs with lengths varying between 18 and 25 nucleotides. Unlike the evolutionarily conserved long-noncoding RNAs (lncRNAs), miRs are numerous and involved in various genetic networks.[101,102] Furthermore, miRs can mediate post-transcriptional gene silencing by binding to target mRNAsvia complementary sequences[103] and then modulate mRNA and protein expression among various kinds of cancers.[104] Recently, growing evidence has shown that miRscan be encapsulated in secreted exosomes and disseminate through the extracellular fluid to reach remote target cells.[105,106] In this review, we utilized the TargetScan, miRanda, miRDB, and PicTar databases to predict targets of the BrCa cell-derived exosomal miRNAs. After screening for potential mRNAs, Gene Ontology enrichment analysis was applied to investigate the major functional categories represented in the aforementioned genes (Figure 3), which would benefit the in-depth research of exosomal miRs in BrCa and help locate the most efficient biomarkers for clinicians.

Figure 3.

Summary of the target gene of miRs. The potential function of the miRs (miR-21, miR-101, miR-105, miR-372, miR-373, miR-451, miR-1246, and miR-222-3p) encapsulated in the BrCa cell-derived exosomes.

Exosomal lncRNA in BrCa Diagnosis

Long-noncoding RNAs, at least 20 bp to 100 kb in length, play an important part in many fundamental cellular processes such as chromatin organization, gene transcription, mRNA turnover, and protein translation, and their deregulation is considered to contribute to carcinogenesis.[107,108] In addition, exosomal lncRNAs may participate in the dissemination of cell signals to regulate local cellular microenvironments. Koldemir[91] and his group found that growth arrest specific 5 (GAS5), an inhibitor of cell proliferation and promoter of apoptosis, accumulated in exosomes in BrCa cell lines (MCF-7 and MDA-MB-231 cell). In their research, they tracked exosomal GAS5 and assessed the efficacy of therapeutic interventions. The results proved that the accumulation of exosomal GAS5 may represent cell apoptosis and also represent a way to evaluate treatment with radiotherapy and many chemotherapeutic agents. The latest research also found that BrCa cell-derived exosomes could regulate the progression of BrCa by delivering the long-noncoding RNA metastasis-associated lung adenocarcinoma transcript 1 (MALAT1),[92] which may indicate that exosomal MALAT1 would be a novel strategy for overcoming BrCa.

Non-BrCa Cell-Derived Exosomes in BrCa Diagnosis

Exosomes are secreted into the extracellular space and efflux into the bloodstream, where they mediate intercellular communication in a very distant way. Hence, non-BrCa cells in this microenvironment will transfer their molecular characteristics to BrCa cells, and this information can serve as a potential source for detecting biomarkers ( ). Mei Yang and colleagues[109] verified that exosomal miRNAs may be transported from macrophages to BrCa cells under a co-culture system of IL-4-activated macrophages and BrCa cells. Macrophage-derived exosomal miR-223 was significantly elevated in co-cultivation with BrCa cells (SKBR3 and MDA-MB-231 cells) and regulated the invasiveness of BrCa cells.

Table 3.

Non-BrCa Cell Content Regulation.

Exosomal Contents	Origin	Isolation/Detection Method	Application	Ref.
miR-233	Human macrophages	RT-qPCR	Promotes breast cancer cell invasion	Yang et al [109]
The quantity of exosomes	Human mammary epithelial cell line(HMEC B42)	Nanosight LM10 analysis, western blot and PKH labeled	Regulate BrCa cell derived exosomes released	Riches et al [110]
ADAM10	Fibroblast	Antibodies and qRT-PCR primers or primer/probe sets	Breast cancer cell mobilization and proliferation	Shimoda M et al,[111,112]
miR-21, -378e, and -143	Cancer-associated fibroblasts	qRT-PCR	Breast cancer epithelial-mesenchymal transition	Donnarumma et al [89]
miR-16	Mesenchymal stem cells	qRT-PCR	Inhibition of angiogenesis	Lee et al [113]

Abbreviation: RT-qPCR, real-time quantitative polymerase chain reaction.

Andrew Riches et al [110] demonstrated that labeled exosomes from either normal or BrCa cells are incorporated into both normal and cancer cells. Thus, there is a clear interaction of exosomes derived from the extracellular environment with tumor cells and normal cells. At the same time, exosomes from normal mammary epithelial cells markedly inhibit exosome release from BrCa cells. This represents a new regulatory pathway for the feedback control of exosome concentrations. It also seems likely that this is a generic mechanism and may be important for other tumor types.

Evidence suggesting that cancer-associated fibroblast (CAF)-derived exosomes may promote cancer cell motility and metastasis is supported in studies wherein ADAM10-rich exosomes were found to promote the activation of oncogenic signaling.[111,112] Numerous studies demonstrated that the CAF-like cell state may determine the role of the tissue inhibitor of metalloproteinases family in the maintenance of the extracellular matrix. It must be emphasized that ADAM10-rich exosomes secreted by human CAFs could enhance cell motility and stimulate cancer cell growth through RhoA and the Notch signaling pathway. Tissue inhibitor of metalloproteinases suppress cancer stroma, while activated fibroblast-secreted exosomes influence tumor progression.

The level of communication between cells is leading to a greater appreciation of the implications of intratumoral heterogeneity and the role of the tumor microenvironment and vasculaturein cancer progression and metastasis.[89] Exosomes are emerging as a crucial mediator of cell-to-cell communication in cancer, thus affecting BrCa progression. Three miRs increased evidently in exosomes from CAFs when compared with normal fibroblasts. Donnarumma et al [114] showed that CAF-secreted exosomal ongogenic miR (miR-21, -378e, and -143) could significantly increase the form of mammospheres, improve stem cell and epithelial-mesenchymal transition markers, and promote BrCa progression.

Mesenchymal stem cells (MSCs), which potentially differentiate into multiple cell types, have the capability of migrating to tumor sites and exerting complex effects on tumor progression. The potential mechanisms and roles within the tumor microenvironment have been elucidated by the scientists, such as immune modulation[113,115] and regulation of the secreted factors of MSCs. Nevertheless, the paracrine effects of MSC-derived exosomes on the tumor microenvironment are unknown and remain to be explored. Jong-Kuen Lee et al [116] showed that MSC-derived exosomal miR-16 may decrease the expression of vascular endothelial growth factor extensively in tumor cells and subsequently inhibit angiogenesis in vitro and in vivo. Additionally, Koumangoye et al [117] proved that the detachment of adherent cells from various substrata may trigger a rapid and substantial secretion of exosomes, which aggregate on the cell surface and mediate adhesion to various extracellular matrix proteins. In brief, these data indicate that cellular detachment is accompanied by a significant release of exosomes, and at the same time, cellular adhesion and spreading are enhanced by the rapid uptake and disposition of exosomes on the cell surface.

Conclusion

The early detection of metastases and micro metastases using multiple exosomal biomarkers would be advantageous for the patient. The field of exosome detection is characterized by the exploration of novel candidate biomarkers and represents a growing field of research. In addition, a large amount of possible circulating indicators provides a new perspective for surgery-free cancer characterization, while realistically, the application of BrCa tissue-based samples represents now or in the near future an indispensable method for setting up valid genomic-based clinical considerations. More importantly, the quantity of circulating biomarkers is growing almost exponentially, and some of the biomarkers, such as miRs and certain proteins, demonstrate an intriguing ability to distinguish among different cancer subtypes. In BrCa, this profile deserves particular attention because of the high heterogeneity of carcinomas. Although clinical trial studies of exosomes in BrCa are little reported,[118] there has been a clinical trial underway for 6 years that has been documented in the web site at https://clinicaltrials.gov (NCT01344109). Other clinical trials have studied the pathogenic and metastatic role of melanoma, colon cancer, lung cancer prostate cancer cell, and pancreatic cancer-derived exosomes (NCT02310451, NCT01294072, NCT03108677, NCT02702856, and NCT02393703), encouraging the use of exosome studies for BrCa. Despite promising results, different kinds of BrCa cell lines or non-neoplastic cell types are known to release different kinds of exosomes, and the high expense of isolation from body fluids has made the clinical application challenging. Additionally, a standard isolation protocol does not exist in the currently available articles. Nevertheless, we still hold that exosomes have opened new avenues in BrCa diagnosis and prognosis due to the minimal invasiveness of sampling and the stability of the bilipid membrane, which makes liquid biopsies repeatable. Additionally, in the development of immunotherapy for high immunogenicity of the most aggressive BrCa subvariants, a specific circulating biomarker might provide more comprehensive information on the immune characteristics of patients with BrCa, which would be extremely useful.