Prostate cancer (PCa) is the most common cancer—excluding skin tumors—in men older than 50 years of age. Over time, the ability to diagnose PCa has improved considerably, mainly due to the introduction of prostate-specific antigen (PSA) in the clinical routine. However, it is important to take into account that although PSA is a highly organ-specific marker, it is not cancer-specific. This shortcoming suggests the need to find new and more specific molecular markers. Several emerging PCa biomarkers have been evaluated or are being assessed for their potential use. There is increasing interest in the prospective use of extracellular vesicles as specific markers; it is well known that the content of vesicles is dependent on their cellular origin and is strongly related to the stimulus that triggers the release of the vesicles. Consequently, the identification of a disease-specific molecule (protein, lipid or RNA) associated with vesicles could facilitate their use as novel biological markers. The present review describes several in vitro studies that demonstrate the role of vesicles in PCa progression and several in vivo studies that highlight the potential use of vesicles as PCa biomarkers.

1. Prostate Cancer

The prostate is an exocrine gland in the male reproductive system that is responsible for the production of seminal/prostatic fluid, a liquid that usually constitutes 50–70% of the semen volume (along with seminal vesicle fluid and, of course, spermatozoa) [1]. The mature prostate gland is composed of columnar and polarized cells lining the prostatic lumen and more elongated basal epithelial cells that separate the lumen from the stroma [2, 3]; both basal and luminal epithelial cells can mutate, thus causing prostate cancer (PCa) [2].

As with all types of cancer, PCa is the result of genetic and epigenetic alterations that induce transformations of normal glandular epithelia [4]. The dysregulation of many molecules and genes has been implicated in PCa; some of these molecules (e.g., NKX3.1, FOXA1, and Myc) seem to be relevant for cancer initiation because their expression is altered during the early stages; other pathways (TMPRSS2-ERG and RB) seem to be involved in the transition from PCa to CRPC. The PI3 K, Akt, PTEN, and mTOR are always dysregulated in PCa [2].

With regard to epigenetic alterations, both hypo- and hypermethylation are well documented. Hypermethylation is common in PCa and is believed to play a role in PCa initiation and progression; hypermethylation of the GSTP1 gene promoter (which can involve the 5V region or CpG islands) is a highly specific marker for PCa, but it lacks sensitivity [5]. The dysregulation of gene expression in PCa appears to be due to changes in chromatin remodeling as well as posttranslational modifications of histones, with several histone-modifying enzymes (namely, HDACs, HMTs, and HDMs) being altered. Changes in miRNA levels are also important in PCa progression, as demonstrated by the role of miRNAs in blocking apoptosis, cell-cycle promotion, migration, invasion, and the maintenance of androgen-independent growth [6, 7].

Among nonskin cancers, PCa is the most common cancer in men older than 50 years of age [8, 9]. The etiology of PCa has not been fully elucidated; however, its risk factors are well-established and include age (incidence and mortality rates increase exponentially after 50 years of age), ethnicity (African Americans have the highest rates), and a family history of PCa (men with fathers or brothers affected by PCa have double the risk of developing this form of cancer) [8, 10, 11]. Other risk factors are likely involved, such as genetic susceptibility, and there is strong evidence from migrant studies that hormones, smoking, diet, sexual factors, and other lifestyle factors also play roles in the development of PCa [8, 10, 12, 13]; among all of these risk factors, diet seems to play a major role in the initiation, promotion, and progression of prostate cancer [13].

PCa incidence rates are generally higher in North America when compared to Western Europe, Oceania, and Asia, but the rates have increased considerably worldwide during the past half century, largely due to the advent of prostatic specific antigen (PSA) testing and its increased use, which has greatly improved diagnosis of this pathology and has highlighted an increased number of cases [14, 15]. At the same time, the extensive use of PSA screening accounts for a great reduction in the proportion of men who present with metastatic disease at the time of diagnosis and the lower mortality rate in some populations [16].

PSA is a serine protease that was first identified in 1966 in seminal fluid; in 1979, its role as tumor marker was first described. Some years later, it was approved by the U.S. Food and Drug Administration for monitoring the disease status of recurrence after definitive treatment in men with PCa, and it is now used to identify men with PCa. It seems, moreover, that PSA can even identify men who are at risk of developing PCa [17, 18]. PSA exists in the bloodstream in several specific forms, including free and complexed (e.g., α-1-antichymotrypsin) forms; free PSA is composed of three isoforms: i-PSA (inactive PSA), pro-PSA (proenzyme PSA), and BPH-PSA (benign prostatic hyperplasia-PSA). The measurement of total PSA and its specific forms can help to differentiate between malign (PCa) and benign conditions [17, 18].

In the blood of patients with either benign prostatic hyperplasia (BPH) or PCa, the prevailing form is the complexed form, whereas the ratio of free/total PSA is lower in PCa than in BPH. BPH-PSA and i-PSA are relatively more abundant than pro-PSA in BPH, whereas in PCa, the reverse is observed [17, 18]. It seems that higher levels of pro-PSA are associated with a higher risk for PCa in men with total PSA levels of 4–10 ng/mL [19] and with more aggressive forms of PCa, as characterized by Gleason scores ≥7 or extracapsular tumor extension [20]. The Gleason score is used to grade PCa, and it is based on the microscopic appearance of cancer tissue, which takes into account the differentiation grade of the tissue. Cancers with higher Gleason scores are more aggressive and have worse prognoses than cancers with lower scores [21].

PSA analysis in serum accompanied by digital rectal examination has been the standard method for PCa screening. Although PSA is highly organ-specific, it is not a cancer-specific marker because it cannot distinguish among indolent PCa, aggressive PCa, and benign conditions (e.g., prostate inflammation is characterized by increased levels of PSA) [18, 22]. PSA levels can even be altered by ejaculation, drugs, or prostate manipulation (particularly by catheterization or prostatic massage), thus contributing to false positives that lead to unnecessary biopsies or other clinical interventions [17, 23].

Nevertheless, in the last few years, mortality specifically attributable to PCa decreased in some countries (such as the US, Canada, Germany, Italy, Switzerland, France, and Spain). As already stated, this decrease is likely due to the introduction of PSA screening, which allows the detection of PCa at an early stage, allowing early curative treatments and improving clinical outcomes. At the same time, new surgical approaches, improved irradiation protocols, and antiandrogenic therapies likely have contributed to mortality decrease as well [24]. Antiandrogenic therapy is important because PCa depends on androgen receptor activity at all stages; standard treatment strategies for disseminated cancer are based on targeting this pathway using androgen deprivation therapy (ADT) or androgen receptor antagonists. Despite such interventions, a successful treatment effect is often followed by reactivation of the androgen receptors, leading to a recurrence of PCa (so-called “castrate-resistant PCa” or CRPC) [2].

2. Extracellular Vesicles

It is now widely known that cells are able to release several types of extracellular vesicles [2528] that are not merely a form of waste elimination, as it was thought when they were discovered; instead, they act as signaling packages and are able to affect neighboring cells and the surrounding microenvironment with the messages they convey [29]. The involvement of extracellular vesicles in various physiological and pathological events, such as the immune response, cellular differentiation, and vascular and cancer pathologies, is also clear [30]. How extracellular vesicles interact with target cells remains to be fully elucidated, even if several hypotheses have been proposed—for example, direct cellular contact mediated by the interaction of membranes with target cell receptors, fusion with the plasma membrane, or encapsulation by endocytosis [26, 31].

Usually, extracellular vesicles can be isolated in vivo from all bodily fluids (e.g., blood, urine, semen, amniotic fluid, saliva, synovial and bronchoalveolar fluids, breast milk, spinal fluid, ascites, and malignant pleural effusion) [22, 32], particularly if they are exposed to primary tumors [33, 34].

The most important extracellular vesicles released from cells are apoptotic bodies, exosomes, and shed microvesicles (MVs) (Figure 1) [2527]. Extracellular vesicles differ mainly in their cellular origins and sizes. Apoptotic bodies are released from the cell membrane as the final consequence of cell fragmentation during apoptosis, and they have irregular shapes with a range of 1–5 μm in size [26, 27]. Exosomes are released by the fusion of multivesicular bodies (MVB) with the plasma membrane and are 30–100 nm in size [26, 27]. Shed MVs are released through regulated outward budding or blebbing of the plasma membrane; they are heterogeneous in shape and are 100–1,000 nm in size [26, 27].

In addition to the well-defined differences in cell origin and size, extracellular vesicles can also exhibit differences or show overlapping features in their molecular compositions and functions. We will further discuss exosomes and MVs, which are released from viable cells and are primarily involved in cell-to-cell communication.

The membranes of exosomes are composed of several lipids, including cholesterol, ceramide, and sphingomyelin, and they are specifically characterized by low levels of phosphatidylserine exposure [26]. The contents of exosomes include mRNA, microRNA (miRNA), and several proteins (ranging from cytoskeletal proteins and adhesion molecules to proteins involved in signal transduction, transcription regulation, and antigen presentation) [35, 36].

Exosomes, secreted both in vitro and in vivo, are involved in intercellular communication in both physiological as well as pathological processes (i.e., cancer) [27, 37] with the following effects.(i)Immune system modulation. Exosomes are variously involved in immune system functions and show either stimulatory or inhibitory effects, acting in antigen presentation or mediating immune tolerance [38, 39]. Exosomes constitutively released from syncytiotrophoblasts, for example, play a role in promoting fetal survival, contributing to other mechanisms that provide maternal immune tolerance of a fetus [40].(ii)Regulation of neuronal cell functions. Some authors have suggested that exosomes from microglia may provide an effective means of intercellular neural communication, which would be very useful considering the limited motility of such cells [41]. It has also been shown that exosomes released from oligodendroglial cells seem to be involved in the trophic support of axons and to contribute to a balanced production of proteins and lipids for myelin [42].(iii)Cancer progression. Tumor cells release exosomes, which can contribute to metastasis and cancer progression. Exosomes are involved in adhesion to the substratum, an important feature for metastatic cells [43], and in angiogenesis induction [44]; moreover, they contain and deliver prooncogenic miRNA to target cells [45]. Adipose tissue-derived mesenchymal stem cells treated with tumor-derived exosomes adopt a myofibroblast phenotype, and myofibroblasts are important tumor-supporting cells [46]; Fas-L-expressing exosomes induce apoptosis in T cells, playing a role in tumor immune evasion [39]. Exosomes are also involved in drug resistance: in drug-resistant human ovarian carcinoma cells, higher cisplatin export via exosomes has been observed [47].

MVs’ membranes are characterized by high levels of phosphatidylserine, which is translocated from the inner to the outer surface leaflet [25], and their cargo includes proteins (e.g., enzymes, growth factors, growth factor receptors, cytokines, and chemokines), lipids, and nucleic acids (mRNA, miRNA, ncRNA, and genomic DNA) [48, 49]. Several studies of the molecular characterization of MVs have suggested that MVs are not simply miniature versions of the parental cells; instead, they show both similarities and differences with respect to the molecular composition of their cells of origin [25, 50]. For example, MVs from human gliomas contain a multitude of molecules that are not detectable or are expressed in different amounts in the parental cells from which they originate [49]. MVs have been widely studied both in normal cell types (including platelets, red blood cells, and endothelial cells) and, more frequently, in cancer cells [27, 5153] for their well-established role in cancer progression. Indeed, MVs contribute to cancer progression in different ways [28], as described below.(i)Contribution to the proinvasive characteristics of cancer cells. Tumor progression and invasion depend on the ability to modify the extracellular matrix. MVs appear to promote the proteolytic cascade required for the localized degradation of the extracellular matrix through the involvement of lytic enzymes, such as uPA, MMPs, and cathepsins, which are contained in MVs [5357].(ii)Apoptosis evasion. Since MVs contain caspase 3, one of the main apoptotic enzymes, it has been suggested that tumor cells may escape apoptosis by releasing MVs enriched with caspase 3, thus preventing its intracellular accumulation [58].(iii)Induction of transformation. MVs derived from human cancer cells (e.g., breast carcinoma and glioma cells) are able to transform normal fibroblasts and epithelial cells to adopt typical cancer cell characteristics (e.g., anchorage-independent growth and enhanced survival capability) through the transfer of the tissue-transglutaminase enzyme [59].(iv)Drug resistance. Some antitumoral drugs accumulate in MVs and are expelled through them [60].(v)Contribution to immunoescape. MVs mediate interactions between cancer and immune cells to modulate the immune response. MVs can carry Fas ligand, resulting in T-cell apoptosis and consequently preventing their cytotoxic effects on tumor cells [61]. The fusion of MVs from human melanomas and colorectal carcinomas with monocytes inhibits differentiation and promotes immunosuppressive cytokine release [62]. MV-associated CD46, a membrane complement inhibitor, helps cancer cells to escape from complement-induced lysis [63].(vi)Induction of angiogenesis. It is well known that tumor growth and survival depend on the formation of new blood vessels (i.e., angiogenesis) that infiltrate the tumor mass [64]. MV-associated EGFR can activate the VEGF/VEGFR pathway in endothelial cells [65]; MVs are a rich source of proangiogenic growth factors, such as VEGF, FGF-2, and proteases (e.g., uPA, MMPs, and cathepsin B) [52, 53, 6669], and of the MMP stimulant EMMPRIN [70]. Lytic enzymes can favor angiogenesis and new vessel formation by carrying out degradation of the basal membrane and the extracellular matrix.

Therefore, despite clear differences in cell origins and size ranges, the specific functions and features of the different extracellular vesicle subpopulations are often overlapping and ambiguous; moreover, difficulties related to the available isolation techniques make it difficult to precisely separate the subpopulations of MVs, thereby preventing the investigation of their specific characteristics.

To further amplify the confusion about the identity of the vesicle subpopulations, in seminal/prostatic fluid, another population of vesicles called prostasomes is present [22]. Prostasomes are derived from the prostate gland and are present in high concentrations in seminal/prostatic fluid; they range in size from 50 to 500 nm (with a mean diameter of 150 nm) [22]. Prostasomes share origins with exosomes because they are stored in the MVBs of epithelial cells lining the acinar ducts of the prostate gland and are released after MVB fusion with the cell membrane [71]. Despite their overlapping origins, exosomes and prostasomes differ not only in size (as already mentioned) but also in composition: the membrane surrounding prostasomes has a specific composition with a higher concentration of cholesterol and sphingomyelin and a substantially high cholesterol/phospholipid ratio when compared to exosomes [22, 72, 73]. Furthermore, exosomes are usually characterized by a bilayer of membranes, whereas prostasomes can have a multilayer membrane [74]. Moreover, in prostasomes, chromosomal DNA, which appears to be absent in exosomes, has been reported [71, 75]. In addition to lipids and DNA, the cargo of prostasomes could also consist of proteins, such as enzymes, transport proteins, structural proteins, signal transduction proteins, and GTP-binding proteins [76].

It is not clear, however, whether prostasomes isolated in vivo from seminal/prostatic fluid correspond to vesicles that are isolated in vitro. Some authors state that in prostate secretion, only exosomes and prostasomes are present [77], whereas others have hypothesized that prostasomes are exosomes derived from prostate cells in biological conditions [22], and others consider them as belonging to the “exosome family” [71]. Like exosomes and MVs, prostasomes are involved in the exchange of information, specifically from prostate cells to other cells (in physiological conditions, recipient cells are mainly spermatozoa) [78]. Transfers of messages can involve several mechanisms, such as fusion or direct contact between the prostasome and the sperm cell membrane, initiating the internalization of prostasomes by the sperm cell [78]. Regarding their biological function, prostasomes seem to be involved mainly in human reproduction; they have a stimulatory effect on spermatozoa motility (showing a promotional effect), capacitation, and the acrosome reaction (i.e., having a regulatory role involving cholesterol transfer) as well as modulation of immunologic attacks (i.e., protecting spermatozoa from phagocytosis performed by the female’s immune cells); they also show antioxidant capacities (reducing reactive oxygen species production, to which human spermatozoa are very sensitive) and antibacterial properties (inducing bacterial membrane deformation) [7881]. In addition to their physiological role in reproduction, prostasomes also appear to be involved in PCa progression [78].

In fact, prostasomes are released not only from normal prostate cells but also from benign prostate tissue, prostate cancer cells, and poorly differentiated cells of prostate cancer metastases [81, 82]. It was suggested that prostasomes contributed to the development of PCa because they were observed in secretions from the prostate (a cancer with a very high incidence) but not in seminal vesicle secretion (which is, indeed, a cancer extremely rare) [78].

Several authors have suggested that some features of prostasomes that may have developed to sustain their physiological role in reproduction could also promote cancer cell survival and proliferation [83]. The following are several roles that have been proposed for prostasomes in cancer progression.(i)Inhibition of the immune system. Prostasomes inhibit mitogen-induced proliferation in a dose-dependent manner in cytotoxic T lymphocytes; therefore, they could most likely interfere with their role (i.e., the recognition of antigens expressed on tumor cells) [84].(ii)Inhibition of the complement system. The complement system is involved in immune surveillance against tumor development. If cancer cells are unable to protect themselves against complement attack, they will be eliminated very early during the development of cancer. The phosphorylation of C3, a component of the complement system, results in the inhibition of both the classical and alternative pathways of complement activation [85]. PCa prostasomes are characterized by higher activities of protein kinases A and C and casein kinase II when compared to prostasomes isolated from seminal plasma. Consequently, they are able to phosphorylate the C3 component, thus inhibiting the complement [86]. Cancer prostasomes also may inhibit complement through an alternative mechanism: by expressing CD59, a glycosylphosphatidylinositol-anchored protein that prevents the full assembly of the membrane-attack complex of complements, they inhibit complement-mediated lysis [87]. Again, prostasomes from cancer cells express higher CD59 levels than those from normal cells [87].(iii)Induction of migration. Protein kinases A and C and casein kinase contained in prostasomes from PCa are able to perform fibrinogen phosphorylation. Fibrinogen phosphorylation inhibits fibrinolysis, making fibrinogen more resistant to cleavage and thereby more available as a substrate for cancer cells, easing their migration [78]. Additionally, prostasomes from PCa express high levels of tissue factor (TF) [88], which is known for its ability to promote cell migration [89] and is also involved in cancer progression due to its ability to induce tumor angiogenesis, cell adhesion, and invasion. Consequently, prostasome-associated TF may further contribute to tumor growth [78].(iv)Induction of invasion. Dipeptidyl peptidase IV is associated with prostasomes and is involved in the proteolytic cascade required for cancer progression through the ECM because the activation of plasminogen and expression of MMP-9 seem to depend on the activity of dipeptidyl peptidase IV [83].(v)Induction of angiogenesis. As has already been mentioned, tissue factor is able to promote angiogenesis through FVIIa-induced VEGF expression. VEGF is a key regulator of angiogenesis due to its ability to stimulate proliferation and migration in endothelial cells [90]. Another important molecule in inducing angiogenesis is angiotensin II, which is produced from the precursor angiotensin I by the action of the angiotensin-1 converting enzyme (ACE) [91]; ACE activity is very high in seminal fluid, and it is mainly associated with the prostasomal membrane [83].

So, prostasomes, which normally have a fundamental role in physiological processes related to fertilization, might turn against the host, favoring the transition of normal cells to cancer cells. The transition from positive to negative action seems to take place at approximately 50 years of age. This is likely why a higher prevalence of PCa is observed in men over 50 years [83].

3. Extracellular Vesicles in Prostate Cancers

Similarly to other cell types, PCa cells are able to release extracellular vesicles (Figures 2 and 3). Nevertheless, only a few in vitro studies in the literature refer to the role played by vesicles released from the PCa cells, highlighting their roles in cell-to-cell communication in cancer progression.

A deep proteomic analysis performed on vesicles from the PC3 cell line revealed that vesicles contain numerous proteins involved in the regulation of several biological processes, ranging from transport to metabolic process, response to stimuli, and cell differentiation and communication. Many were nuclear and cytosol proteins, but numerous cytoskeleton proteins were also present. Among these proteins, CDCP1 and CD151, whose involvement in PCa has already been described, stand out as possible biomarkers considering that they were more concentrated in vesicles released by prostate cancer cells than in those released by normal epithelial prostate cells [92].

PCa-derived vesicles stimulate fibroblast activation, a fundamental requirement for the induction of a favorable niche for cancer development, by increasing their motility and protecting them from apoptosis—events that are partially due to an increase in ERK1/2 phosphorylation. Vesicles from fibroblasts thus activated are, in turn, able to induce migration and invasion in the PC3 cell line, supporting cancer pathogenicity. It seems that the chemokine receptor CX3CR1 also plays a role in this process [93].

PCa tissue releases MVs capable of degrading collagen IV and the reconstituted basal membrane Matrigel. MVs released from PC3 cells (a highly metastatic PCa cell line) have been found to enhance the adhesive and invasive capabilities of LnCaP (a poorly invasive PCa cell line) [67].

It was also suggested that vesicles from hormone-refractory PCa cells are able to induce mouse osteoblast differentiation via Ets1 contained in them, suggesting a role for vesicles in cell-to-cell communication during the osteoblastic metastasis process [94]. It is well known that in osteoblastic metastasis, a vicious circle develops between PCa cells and osteoblasts/osteoclasts, with PCa cells providing growth factors to osteoblasts and osteolytic factors (e.g., BMPs, TGF-β, IGF, FGF, PDGF, ET1, VEGF, and MMPs) that activate these cells and allow them to produce bone-derived growth factors (e.g., PDGF, BMPs, TGFβ, IGFs, and FGFs) that further induce cancer-cell stimulation [94, 95]. Moreover, the release of vesicles from PCa cells is induced from osteoblast-conditioned media, further suggesting that vesicles contribute to communication between cells in the course of this vicious circle [96].

A recent study highlights the role of vesicles in tumor microenvironment cell-to-cell communication, showing that vesicles released from the human prostate carcinoma cell line DU145 are able to induce transformation in the nonmalignant human prostate epithelial cell line, as evidenced by anchorage-independent growth in soft agar which is a typical feature of malignant cells. Additionally, vesicles isolated from PCa patients with a Gleason grade of 2 have similarly been used to treat nonmalignant prostate cells and have induced soft agar colony formation. The same study, however, suggested that vesicles could potentially be used to reverse the cancer phenotype because vesicles isolated from nonmalignant cells inhibited the growth of carcinoma cells in soft agar.

PCa vesicles are also involved in drug resistance: DU145 cells, which are normally sensitive to camptothecin treatment, became resistant to camptothecin-induced apoptosis after being cocultured with vesicles isolated from the camptothecin-resistant cell line RC1. Conversely, RC1 cells, cocultured with vesicles isolated from DU145, underwent apoptosis when treated with camptothecin, suggesting the role of vesicles in mediating drug resistance. Several molecules seem to be involved in these processes, including SOCS3 and STAT3 [97].

In addition to the in vitro studies that have tried to understand the roles played by vesicles in cancer progression, several in vivo studies have been performed to understand whether vesicle number or some vesicle-associated molecules could be used for diagnosis and prognosis. Although PSA is currently considered the gold standard for the detection of PCa, it is important to take into account not only PSA’s high organ specificity but also its lack of cancer specificity. PSA also gives no indication about the proliferation and metastatic potential of prostate cancer cells [78], hence the need to find new and more specific molecular markers to assist or replace PSA.

To this end, PCa was studied indirectly by analyzing biological fluids in a search for useful protein, DNA, and RNA markers [5]. Several emerging biomarkers have been evaluated or are being assessed for their potential use. Biomarker research looks at all useful specimens, as identified below.(i)Prostate tissue. Tissues from PCa have been studied not only to understand PCa pathophysiology but also to find new biomarkers. The reliability of this strategy, however, is based on the correct tissue sampling: if the biopsy misses the tumor, even an optimal biomarker will fail to detect cancer [98]. Several molecules from prostate tissue are possible candidates, such as Ki-67, p53, Bcl-2, AMACR, PSMA, BMP-6, PTEN, NF-κB, CYCS, ICK, IKBKB, GAD1, CD10, and syndecan-1 [5].(ii)Blood. Several useful techniques, ranging from ELISA to capillary electrophoresis coupled to mass spectrometry, are being studied to facilitate the accurate evaluation of plausible markers. Such studies have shown, however, that blood may present some technical problems in tissue sampling that may make it an unreliable source of biomarkers—this point follows from the fact that the amount of proteins being studied may depend on several factors (such as clotting time). Consequently, the use of serum or plasma may be more advisable [98]. Some blood markers are EPCA and PSCA; serum markers include Crisp-3, hK2, OPG, CGA, TGF-β, hK2, IL-6, Cav-1, E-cadherin, EGFR, VEGF, von Willebrand factor, alpha-1 chymotrypsin, vilin, hepsin, neuron-specific enolase, β-catenin, and hK11 [5].(iii)Urine. The use of urine for sampling has several obvious advantages. Samples are abundant, they are obtainable in a noninvasive way, and they have greater stability than tissue or blood samples; moreover, there are no difficulties related to sampling. Because urine can contain both exfoliated PCa cells and PCa-secreted products, it could be considered a potential source of markers for early detection [98]. Useful markers are TMPRSS2-ERG oncogenic gene fusion rearrangement, PCA3/DD3, Survivin, telomerase, Tb15, Bradeion, MCM-5, hepsin, δ-catenin, Lgals3, CFB, Apo-D, RECK, PECAM1, and others [5, 23, 99].(iv)Seminal plasma. As with urine, seminal plasma has the advantage of being easily accessible and highly stable. Several biomarker candidates (N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase, prostatic acid phosphatase, stabilin-2, GTPase IMAP family member 6, and semenogelins-1 and -2) have been identified based on differential expression between PCa patients and controls [100].

The possibility of using extracellular vesicles as PCa biomarkers has generated considerable interest. Because the contents of these vesicles include a tumor-enriched repertoire of biomolecules dependent on their cellular origin, strongly related to the stimulus that triggers their release, the discovery of a disease-specific protein, lipid, or RNA associated with the vesicles could make it possible to use them as novel biological markers for prognostic and diagnostic purpose and for monitoring of the disease, not only in PCa but virtually in all types of cancers [22, 50]; indeed, several studies in this direction have been already conducted in several cancer diseases (Table 1). The findings that urine from cancer patient is characterized by elevated exosome secretion [101] and that prostasomes can be detected at higher levels in plasma from PCa patients if compared to patients with nonmalignant prostate pathologies or indolent PCa [71] further support this hypothesis. For the moment, the focus is primarily on vesicle-associated miRNA, which shows great potential in urologic cancers under diagnostic and prognostic profile [102].

miRNAs are short (19–26 nucleotides long), single-stranded, noncoding RNAs that are responsible for the regulation of gene expression at the posttranscriptional level because they inhibit mRNA translation at the initiation or elongation step, thereby blocking the translation of mRNAs into corresponding proteins [109]. Changes in miRNA expression mainly affect cell proliferation, apoptosis, differentiation, and cell-cycle regulation, thus explaining the role that miRNA plays in tumor cell survival and growth, which are undoubtedly involved in cancer development and progression [110, 111]. The consequences of changes in miRNA levels include the altered expression of target oncogenes and tumor suppressor genes. Indeed, it has been widely shown that a substantial number of miRNAs that normally act as tumor suppressors are downregulated in cancer cells, whereas miRNAs normally acting as oncogenes are expressed at higher levels in cancer cells [32, 112]. It was also demonstrated in vitro that associated exosomal miRNAs can downregulate their target genes in recipient cells [113].

Over the years, several miRNAs have been studied for their biological role in PCa. For example, miR-20a and miR-125b are oncogenic miRNAs that have antiapoptotic and pro-survival effects, respectively, in PCa cells. miR-221 and miR-222 contribute to cancer growth; miR-126 acts as tumor suppressor, and its loss could contribute to PCa progression. Additionally, miR-146a is a tumor suppressor [111].

Because miRNAs are attractive as potential diagnostic/prognostic PCa biomarkers and may potentially be used to monitor treatment response, their levels and profiles have been studied in PCa tissue and compared with healthy tissue [32, 102, 114]. Fifteen miRNAs have been observed to be differentially expressed in PCa and benign tissue and demonstrate up to 84% accuracy for discrimination between these categories; 10 of these 15 miRNAs (namely, miR-16, miR-31, miR-125b, miR-145, miR-149, miR-181b, miR-184, miR-205, miR-221, and miR-222) exhibit downregulation, whereas the remaining 5 (namely, miR-96, miR-182, miR-182*, miR-183, and miR-375) exhibit upregulation. miR-96 expression, moreover, has been associated with cancer recurrence after radical prostatectomy [115].

It is important to keep in mind that miRNAs are not only present within cells but they can also be released in vitro into cell culture media. Moreover, miRNAs have been identified in vivo in several biological fluids, such as blood, urine, breast milk, and seminal plasma [32, 116]. Although controversy has existed over whether miRNAs circulate freely or are encapsulated in vesicles, some studies have demonstrated that in biological fluids (specifically saliva and urine), the concentration of miRNAs was consistently higher in vesicles (especially exosomes) compared to the vesicle-depleted supernatant [117]. miRNAs can also be contained in apoptotic bodies and high-density lipoproteins or associated with Ago1 and Ago2 proteins; all of these forms of association are likely responsible for protecting the molecules from degradation secondary to RNase treatment [32, 102].

A large number of studies have evaluated the presence of miRNAs in serum or plasma, assessing the differences between PCa patients and healthy controls [32]. miR-375 and miR-141 have been demonstrated to be the most consistently associated with the pathological stage and Gleason score [102, 116]; their levels are higher in the serum of patients with castration-resistant prostate cancer than in the serum of low-risk, localized patients [118]. Additionally, miR-141 levels have been able to distinguish patients with prostate cancer from healthy controls [119].

Some of these studies specifically considered miRNA associated with serum-derived vesicles. Twelve miRNAs were differentially expressed in prostate cancer patients compared with controls, and the levels of 11 miRNAs were significantly increased in PCa patients with metastases compared to patients without metastases (vesicle-associated miRNA-141 and miRNA-375 were confirmed to be associated with metastatic PCa), suggesting that circulating miRNAs could be used to diagnose and stage prostate cancer [120].

Using exosomes as biomarkers contained in urine would be even more preferable. Because urine passes through the prostate before being discharged, miRNA features in urine would reflect the status of tumor cells [102]. When compared to blood, urine offers several advantages. Particularly, the samples can be obtained in a noninvasive way and in large quantities; moreover, the composition of urine is undoubtedly less complex than that of blood, leading to easier sample analyses [32].

Apart from studies on exosome-associated miRNAs, the exosomal content from PCa patient samples has been variably evaluated.

The amount of urinary exosomes decreases after androgen deprivation therapy, and some PCa markers (specifically, PSA, PSMA, and tumor-associated marker T54) have sometimes been detected in urinary exosomes but never in healthy donor samples; in one patient, the decrease of exosomal PSA was clearly related to treatment [101]. Even if the authors admit that the future of urine-exosome analysis in PCa remains uncertain, the use of urinary exosomes could eventually be a noninvasive approach that provides clinically useful information.

RNA expression analyses in urine-derived exosomes from patients with PCa have further confirmed the possibility of using such vesicles for new methods of diagnosis. For example, exosomes from patients with high PSA levels and high Gleason scores expressed the mRNA transcript for the fusion gene TMPRSS2:ERG, whereas PCA3 was detectable in exosomes from all patients (mRNA of TMPRSS2:ERG and PCA3 being PCa biomarkers). TMPRSS2:ERG and PCA3 were not detectable in patients treated with ADT nor in medically castrated or prostatectomized patients with verified bone metastases [77]. The Nilsson study established the potential use of urine-derived exosomal mRNA to obtain information on tumor status. The presence of tumor-specific transcripts in vesicles, moreover, is not limited to PCa but it is also present in other cancers suggesting that tumor-specific transcripts contained in vesicles could serve for diagnostic of cancer diseases; in Ewing’s sarcoma (ES), for example, it has been found that both exosomes and microvesicles contained the ES specific transcript EWS-FLI1, which is not present in healthy donors and might be useful as a noninvasive diagnostic ES marker in peripheral blood [121, 122].

The circulating levels of survivin (a member of the “inhibitor of apoptosis” family), either free or contained in serum/plasma-derived exosomes, have been found to be lower in patients with benign prostatic hyperplasia and in healthy controls when compared to PCa patients. Circulating survivin levels remain high both in subjects with low and high Gleason scores, suggesting that it may be useful as a biomarker even for the earlier detection of PCa [123].

Some studies on prostasomes have shown that they could be used as potential PCa biomarkers. Using a method called 4PLA, which is a variant of the proximity ligand assay and has high sensitivity and specificity for prostasomes, the researchers demonstrated that plasma from PCa patients contains high levels of prostasomes. Moreover, the assay seemed to be able to discriminate between patients with medium and high Gleason score from those with low Gleason score. The authors suggested that the loss of prostate epithelial cell polarity, typical of PCa, could be involved in the modification of prostasome features. This method could potentially be used for early diagnosis or for monitoring responses to treatment [34].

4. Conclusions

Over the years, many studies have been conducted to better understand the role of extracellular vesicles circulating in biological fluids in various clinical tumor conditions and their potential use as biomarkers for prognostic or diagnostic purpose or as vaccine to induce immune response [124, 125]; some clinical studies have been already conducted to evaluate the use of vesicles in this form of immunotherapy (Table 2). The other forms of clinical application of extracellular vesicles need, instead, a further evaluation. Thus, a deeper understanding of the roles of extracellular vesicles in cell-to-cell communication and in prostate cancer biology, as well as continued expansion of the field of vesicle research, may lead to the development of extremely useful vesicular biomarkers for determining the diagnosis or prognosis of cancer. Such biomarkers may serve as valid instruments with which to assess the responses to clinical treatments. However, many questions remain about the effective role of extracellular vesicles in prostate physiological and pathological processes, and further studies are needed to clarify their usefulness as biomarkers. Furthermore, it is necessary to refine the techniques used to isolate and quantify, in blood or other biological fluids, vesicles specifically derived from tumor tissues as well as to standardize sample collection and analytical methodologies.


ACE:Angiotensin-1 converting enzyme
ADT:Androgen deprivation therapy
Akt:Protein kinase B
AMACR:Alpha-methylacyl CoA racemase
Apo-D:Apolipoprotein D
Bcl-2:B-cell lymphoma 2
BMP:Bone morphogenetic protein
BPH:Benign prostatic hyperplasia
Cav-1:Caveolin 1
CFB:Complement factor B
CGA:Chromogranin A
Crisp-3:Cysteine-rich secretory protein 3
CRPC:Castrate-resistant PCa
CX3CR1:Chemokine (C-X3-C motif) receptor 1
CYCS:Cytochrome c, somatic
DCs:Dendritic cells
EGFR:Epithelial growth factor receptor
EMMPRIN:Extracellular matrix metalloproteinase inducer
EPCA:Early prostate cancer antigen
ERK-1:Extracellular regulated kinase 1
ES:Ewing’s sarcoma
ET1:Endothelin 1
EWS/FLI1:Ewing’s sarcoma/Friend leukemia integration 1
FGF:Fibroblast growth factor
GAD1:Glutamate decarboxylase 1
GM-CFS: Granulocyte macrophage colony-stimulating factor
GSTP1:Glutathione S-transferase p1
HDACs:Histone deacetylases
HDM:Histone demethylases
hK11:Human tissue kallikrein 11
hK2:Human kallikrein 2
HMTs:Histone methyltransferases
ICK:Intestinal cell kinase
IGF:Insulin-like growth factor
IKBKB: Inhibitor of NF-κB kinase subunit beta
IL-6:Interleukin 6
LGALS3:Lectin, galactoside-binding, soluble, 3
MAGE:Melanoma-associated antigen
MCM-5:Mini-chromosome maintenance 5
MMPs:Matrix metalloproteinases
mTOR:Mammalian target of rapamycin
MVB:Multivesicular bodies
ncRNA:Noncoding RNA
NF-κB: Nuclear factor-κB
NK:Natural killers
NSCLC:Non-small-cell lung carcinoma
PCa:Prostate cancer
PCA3/DD3:Prostate cancer antigen 3/differential display code 3
PDGF:Platelet-derived growth factor
PECAM1:Platelet endothelial cell adhesion molecule
PI3 K:Phosphatidylinositide 3-kinases
PSA:Prostate-specific antigen
PSCA:Prostate stem cell antigen
PSMA:Prostate-specific membrane antigen
PTEN:Phosphatase and tensin homolog
RECK:Reversion-inducing-cysteine-rich protein with kazal motifs
SOCS3:Suppressor of cytokine signaling 3
STAT3:Signal transducer and activator of transcription 3
Tb15:Thymosin beta 15
TF:Tissue factor
TGF-β:Transforming growth factor-beta
TMPRSS2-ERG:Transmembrane protease serine 2/ETS-related gene
uPA:Urokinase-type plasminogen activator
VEGF:Vascular endothelial growth factor.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.


The authors are grateful to Dr. Marianna Di Francesco (University of L’Aquila) for performing electron microscopy on PC3 cells (scanning electron microscopy) and extracellular vesicles (transmission electron microscopy). The authors also thank Dr. Enzo Emanuele, a holder of both the M.D. and Ph.D. degrees (Living Research s.a.s., Robbio, Pavia, Italy), for his expert editorial assistance.