1Dipartimento di Farmacia-DIFAR,
Correspondence Address: Prof. Isabella Panfoli, Dipartimento di Farmacia-DIFAR, Università di Genova, Scuola di Scienze Mediche e Farmaceutiche, DIFAR, Viale Benedetto XV, 3, Genoa 16132, Italy. E-mail: firstname.lastname@example.org
© The Author(s) 2020. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
Exosomes, nanovesicles of endocytic origin, are secreted by most cell types; cancer cells representing no exception. Exosomes facilitate intercellular communication as they deliver diverse proteins, mRNA, miRNA and lipids. In this review, we discuss how exosomes represent one of the main risks associated with cancer but also one of the most promising new tools to fight it. Exosomes appear to function as signalling molecules between the tumour microenvironment, i.e., the complex of both cancer and stromal cells, and the rest of the body. Cancer-derived exosomes have been shown to drive the initiation and progression of metastasis, by transporting their cargoes to target tissues. In this respect, exosomes are implicated in cancer progression, dissemination and therapy resistance. However, exosomes are also emerging as a key tool in precision medicine, pivotal for cancer liquid biopsy in early diagnosis and for assessing when there is a recurrence. Profiling exosomal cancer-derived nucleic acids by ultrasensitive next-generation sequencing along with mapping the protein profile utilizing high-throughput proteomics will allow earlier cancer detection, therapeutic stratification and monitoring of response to therapy. Exosomes are also a promising new tool for cancer immunotherapy. Clinically utilizing exosomes for these applications in cancer diagnosis and therapeutics will be the next challenge.
Biomarkers, cancer, exosomes, immunotherapy, liquid biopsy, precision medicine, proteomics
Exosomes (Exo) are nanovesicles secreted by virtually any cell and found in all human body fluids[1-4]. They play important roles in intercellular communication both in physiology and disease[4-6]. After being released into the extracellular space, Exo can enter the circulation and ultimately be taken up by recipient cells to which they can convey their protein, nucleic acid and lipid cargo in turn modulating their activity[7,8]. By proteomic and biochemical analyses, we have reported a novel characteristic of human Exo, i.e., they can consume oxygen to aerobically synthesize ATP[9-11]. Proteomic and statistical analyses of both human mesenchymal stem cell (MSC) and urinary Exo showed enrichment of proteins related to aerobic metabolism, including the redox complexes I, IV, and V in their membranes[9-11]. Such aerobic metabolic capacity appears consistent with the Exo need to maintain their cup-shaped structure and functionality in the face of a prolonged permanence in the circulation[10-12] and with their ability to rescue bioenergetics of damaged cells[13,14].
Research in the field of cancer is benefiting from the growing understanding of the biogenesis and functions of Exo released from cancer cells[15-18]. However, the role of Exo in the pathophysiology of cancer is multifaceted. Cancer cell-derived Exo have long been known to be involved in processes such as cancer progression, metastasis, immune escape, angiogenesis and therapy resistance[20,21]. Exo function as signalling molecules between the tumour microenvironment, i.e., the complex of both cancer and stromal cells, and the rest of the body. Tumour-derived Exo can drive the metastatic process by targeting specific organs setting a pre-metastatic environment. The tumour environment reacts by amplifying oncogenic pathways in which Exo signalling is proposed to play a role.
Nonetheless, Exo also contain biomarkers, and can be considered biomarkers themselves[23,24]. For example, urinary Exo deriving from every cell of the urinary tract and kidney, may represent a promising reservoir of cancer biomarkers to assess disease progression in urologic cancers[25,26]. Exo can be noninvasively isolated from human urine to detect biomarkers, with promising applications in patient stratification, monitoring of therapy response or use as vehicles for therapeutic delivery.
Thanks to high throughput mass spectrometry techniques, it can be envisioned that Exo will help in earlier diagnosis, directing therapeutic targets and assessing therapy resistance upon detection of signature cargo biomarker biomolecules[1,16]. In the landscape of precision medicine, cancer liquid biopsies, i.e., the analysis of circulating cell-free tumour DNA and tumour cells (CTC), can exploit examining Exo signatures, when they are derived from biological fluids. Exo can also potentially be used as tumour-targeting vehicles for cancer[17,18,21]. There is also the exciting possibility of engineering the content of Exo and targeting them to tissues of interest[30,31].
This review focuses on the dual role of Exo in cancer. The good side of Exo is their clinical potential. The ability of Exo to mediate cell-to-cell communication as stable carriers of molecular messages can be exploited for cancer diagnosis and therapy, with novel exciting perspectives of translation to the clinical setting[16,32]. The bad side of Exo is the long-recognized ability of their cargo to modify the cancer microenvironment promoting cancer progression and metastasis by recruiting target cells, as is the case for melanoma.
Exo, a subset of extracellular vesicles (EVs) of endocytic origin, actively shed from multivesicular bodies (MVBs) which carry proteins, RNAs (mRNA, miRNA, transfer RNA, ribosomal RNA, nucleolar RNA, and noncoding RNA) and DNA fragments[1,3,7,34]. Exo biogenesis involves the formation of early endosomal vesicles, that develop into late endosomes undergoing inward budding forming intraluminal vesicles (ILVs) in MVBs[6,35]. Exo acquire their luminal and membrane contents through both direct and stochastic sorting. If nascent ILVs are not degraded by fusion with lysosomes, they fuse with the plasma membrane and are released into the extracellular space. Once in the circulation, Exo are directed to other cells via an unclear mechanism, probably involving members of the tetraspannin family (CD9, CD63 and CD81), where they are taken up by the target tissues through membrane fusion, endocytosis, or receptor-ligand interaction[2,34,37,38].
Exo isolation involves a variety of techniques[39,40]. Several commercial exosome isolation kits are in use, although their ability to yield pure and functional Exo is uncertain. To date, differential ultracentrifugation is considered the gold standard, and it is much preferred when pure Exo are required. Low-speed centrifugation subsequent to polyethylene glycol precipitation has been utilized to enrich Exo from large sample volumes, but there is the possibility of polymer contamination. The other Exo isolation methods are size-based, antibody capture-based, microfluidics-based techniques or precipitation by altering Exo solubility with water-excluding polymers such as polyethylene glycol, all of which do not require high-speed centrifugation. Fluidic techniques such as exosome total isolation chip, can sort Exo from a heterogeneous population of EVs based on their size, with the advantage of allowing the handling of small sample volumes. Label-free efficient separation of Exo from human blood has been reported, using an integrated continuous-flow acoustofluidic device. This last automated isolation technique is useful in case of biohazard, and for integration with downstream Exo analysis systems. Notably, most novel isolation methods are limited by the requirement of sophisticated instrumentation or costly reagents. Therefore, notwithstanding their promising potential, a concern about the clinical applications of Exo appears to be the standardization of isolation techniques.
Exo are emerging as promising and sensitive cancer biomarkers for disease diagnosis[21,23,24,26]. Once released from cancer cells, Exo enter the circulation and are transported in biological fluids carrying their functional cargoes. Profiling Exo cancer-derived nucleic acids by ultrasensitive next-generation sequencing and proteins by large-scale high-throughput proteomics could allow early cancer detection, therapeutic stratification and response to therapy monitoring[17,18,38,45,46].
Liquid biopsy has drawn attention as a minimally invasive and cost-effective method for sampling of genetic, proteomic and metabolic material from different types of cancer. While traditional cancer liquid biopsies utilize cell free DNA or CTC, Exo are emerging as a novel tool in the field of precision medicine in the early diagnostic and recurrence assessment applications[24,49]. This has proven true especially for urologic tumours[29,50]. The advantage of Exo over existing approaches is their stability in body fluids allowing the specific cancer-derived proteins and nucleic acids to be preserved[1,4]. For example, a cell membrane-anchored proteoglycan, glypican-1 (GPC1), overexpressed in a variety of cancers such as breast and pancreatic cancer, was also identified in the circulating Exo from the serum of pancreatic cancer-bearing patients. Detection of GPC1+ Exo in the serum can be utilized to distinguish healthy subjects from pancreatic cancer patients with very high specificity and sensitivity, findings that can then be correlated with survival rates. Considering its cited role in the progression of human pancreatic cancer, miR-301a-3p was proposed as a biomarker in the diagnosis of this type of cancer. An Exo-specific “melanoma signature” with prognostic and therapeutic potential has been proposed.
Exo can also become stable and reliable engineered nanocarriers. In fact, the benefits of the use of Exo as therapeutic agents include their biocompatibility and ability to deliver their content to specific target cells, an unfavourable feature per se, that can however be of advantage. The characteristic exosomal membrane stability, which is enriched in cholesterol, sphingomyelin and ceramide, along with its tumour-targeting capacity, has suggested the use of Exo in anticancer therapy delivering therapeutic miRNAs and proteins or as drug delivery system for cancer therapy. Drug delivery with Exo has been utilized for the treatment of breast, pancreatic, lung, and prostate cancers and glioblastoma. Drug loading into Exo can be accomplished by both active and passive encapsulation approaches[55,56]. Passive loading can be accomplished by simple incubation of the Exo with the drug or miRNAs to let them diffuse along the concentration gradient or treating cells with a drug, and using Exo secreted by these donor cells. Active encapsulation can be performed by freeze-thawing cycles, electroporation of the Exo membranes, or sonication in the presence of the drug. Sonication can be also used to encapsulate proteins. Freeze-thawing method has also been utilized to fuse Exo with liposomes, to develop exosome-liposome hybrids carrying specific proteins. By manipulating the shedding process of Exo, these can also be engineered using viral vectors, such as retroviruses and adenoviruses to engineer the parent cells to secrete modified Exo, or alternatively, to directly manipulate the content Exo following secretion[30,56]. The use of Exo also shows significant safety and low toxicity benefits as compared to cell-based therapies, which bear the risk of activation of a host immune response. By contrast, allogenic Exo elicit lower immune response. The use of MSC-derived Exo for delivery of anticancer therapy was shown to hold more promise than the use of MSC themselves. The fact that MSC Exo carry an aerobic metabolic ability may also be taken into closer consideration.
Exo are also a promising new tool of cancer immunotherapy[15,60]. In lieu of dendritic cell (DC)-based cancer immunotherapy, still in its infancy due to problems associated with culture and storage, the use of DC-derived Exo to generate immune responses against tumours, has been proposed. DC-derived Exo possess immunostimulatory properties thanks to the expression of integrins, ICAM-1 and MHC class II and class I molecules as well. Exo stability would maintain the DC-derived Exo cancer antigen composition, including surface MHC-peptide complexes and the CD80 and CD86 costimulatory molecules, thus triggering the desired cancer antigen-specific immune response. DC-derived Exo-based phase I and II clinical trials have demonstrated their ability to target cancer sites.
By genetic modification of the parental cell, Exo can be loaded with a variety of biological molecules, such as miRNAs and proteins. Exo surface modification by addition of ligands or proteins to the Exo surface can direct them to target cancer cells. In this respect, the features that allow Exo to reach their targets (i.e., ligands expressed onto their surface) allow their positive applications. Targeting ligands on the surface of Exo can also be engineered. For example, HEK293T cells were engineered to express the protein Lamp2b, fused to a fragment of interleukin 3 in their Exo membrane, and it was found that these Exo loaded with imatinib or with a specific siRNA were able to target cancer cells and inhibit their growth in vitro and in vivo. Exo released by macrophages, loaded with paclitaxel (PTX) increased the cytotoxicity of PTX by about 50-fold. In vivo, those Exo co-localized with lung metastases causing a significant inhibition of their growth.
The hallmark of the double nature of Exo is their ability to deliver miRNA, small noncoding RNAs that target mRNAs and change their expression. Exo can be manipulated to have them deliver anti-miRNAs, or tumour-suppressing miRNAs for cancer treatment. It was shown that endothelial cells can transfer exogenous miRNA to cancer cells via Exo.
Cancer cells secrete more Exo than healthy cells. Moreover, their contents appear to be tailored to mediate cancer dissemination[8,16,17,23]. Being potent signalling mediators, Exo shed from cancer cells act in facilitating cancer initiation and progression[20,21]. Exo are also secreted by cells in the tumour microenvironment (TME) such as stromal and immune cells[22,66]. TME is the complex setting of the interplay between cells and signalling events, of which Exo along with cytokines and chemokines are key players. In particular, Exo can precondition the TME setting the pre-metastatic niche, which increases metastatic success. Evidence suggests that the contents of Exo modulate immune cell activity, enabling immune surveillance and treatment evasion. For example, Exo were shown to express programmed death-1 (PD-1), which interacts with programmed death-ligand 1 (PD-L1). Upregulation of the expression of PD-L1 receptor on T cells mediates PD-L1-dependent immune evasion, by actively suppressing the function of CD8. It was shown that exosomes expressing PD-L1 shed form metastatic melanomas helping the tumour to evade immune surveillance. Assessment of exosomal PD-L1 content has been proposed to stratify patients for therapy with anti-PD-1 antibodies, a promising treatment for metastatic melanoma. While remaining a poorly understood process, metastasis is the cause of most cancer-related deaths with miRNA transfer to endothelial cells, mediated by Exo, facilitating this metastatic process.
Exosomal mRNA and proteins from prostate cancer cells were shown to modulate the prostatic TME[21,67]. The formation of melanoma lung metastases is preceded by the recruitment of bone marrow progenitors primed through receptor tyrosine kinase MET activation by Exo. Pancreatic cancer cell-derived Exo can induce stellate cells to recruit macrophage subpopulations, establishing a pre-metastatic environment inside the liver[17,33]. Pancreatic cancer cell Exo promote metastasis by inducing the M2 polarization of macrophages through activation of the PTEN/PI3Kg pathway. It was shown that Exo miR301a-3p overexpression is associated with poor survival.
Given that Exo have “good” and “bad” roles (see Schematic in Figure 1), a prerequisite for the successful implementation of their use for cancer therapy requires rigorous isolation, and characterisation. In an attempt to support the standardisation of Extracellular vesicles (EV) in research and clinical applications, an international consortium was established, named “EV-TRACK” (http://evtrack.org). EV-TRACK is a knowledgebase intended to gather and centralize reports on EV biology and methodology.
Exo are nano-sized vesicles secreted from living cells into all body fluids. They bear a dual role in cancer biology, being supportive of cancer progression, by setting the tumour metastatic niche, but are also carriers of cancer cell-specific protein and nucleic acid contents. Exo are viewed as promising tools for cancer diagnosis and therapy. We highlight how current research is exploiting both these utilities and the strategies used to enhance the potential of Exo in the treatment of cancer. If understood in more detail, the identification of cancer-specific Exo would become vital in early diagnosis and assessing response to therapeutic intervention(s) when monitoring cancer progression and its treatment. The unique stability, biocompatibility, homing ability and low immunogenicity of Exo, can also be exploited as a delivery system for therapeutic agents since Exo can also be loaded with a variety of molecules. As our understanding of Exo biology and the profiling of their protein and RNA cargoes as potential biomarkers is expanded, the ability to engineer content of Exo opens new possibilities for their use as selective carriers of therapeutic miRNAs and/or drug carriers to target tumour cells. It is foreseeable that the next years will witness the challenging clinical applications of Exo in cancer diagnosis and therapeutics.
Made substantial contributions to the conception and design of this study and wrote the manuscript: Panfoli I
Revised this work substantially: Bruschi MAvailability of data and materials
Not applicable.Financial support and sponsorship
None.Conflicts of interest
All authors declared that there are no conflicts of interest.Ethical approval and consent to participate
Not applicable.Consent for publication
© The Author(s) 2020.
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Panfoli I, Bruschi M. The good and bad sides of exosomes: pre-metastatic niche formation, cancer biomarker and therapy carriers. J Cancer Metastasis Treat 2020;6:35. http://dx.doi.org/10.20517/2394-4722.2020.50
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