J Cancer 2019; 10(24):6154-6160. doi:10.7150/jca.31752

Review

Potential Therapeutic Roles of Exosomes in Multiple Myeloma: A Systematic Review

Mengzhen Li2*, Bing Xia2*, Yi Wang2,3*, M. James You3 Corresponding address, Yizhuo Zhang1,2 Corresponding address

1. Department of Pediatric oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, Guangdong 510060, China
2. Department of Hematology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer; Key Laboratory of Cancer Prevention and Therapy, Tianjin; Tianjin's Clinical Research Center for Cancer; 300060, China
3. Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA
*Mengzhen Li, Bing Xia and Yi Wang are co-first authors and contributed equally to this work.

This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
Citation:
Li M, Xia B, Wang Y, You MJ, Zhang Y. Potential Therapeutic Roles of Exosomes in Multiple Myeloma: A Systematic Review. J Cancer 2019; 10(24):6154-6160. doi:10.7150/jca.31752. Available from http://www.jcancer.org/v10p6154.htm

File import instruction

Abstract

Multiple myeloma (MM) is the second most prevalent hematological malignancy. In spite of the remarkable progress in understanding the biology and therapy of MM, curing this disease remains difficult, which calls for more effective treatment strategies. As vital communicators between different cells, exosomes have been verified to be crucial to cancer diagnosis, treatment, and prognosis. Exosomes in MM patients show a different expression profile compared with those in healthy individuals. In this review, we summarize potential therapy roles exosomes may play in MM. The specific expression of certain components in exosomes may provide therapeutic targets. Moreover, tumor-derived exosomes and their modified products can be developed into vaccines for anti-tumor immunity. In addition, the natural nano structure of exosomes makes them excellent carriers for drug delivery. Thus, a more rigorous investigation into exosomes will pave the way for novel tumor therapies in MM patients.

Keywords: exosomes, multiple myeloma, potential therapeutic target, miRNA, protein, drug delivery

Introduction

Multiple myeloma, which features with constant clonal expansion of plasma cells in bone marrow (BM), is the second most prevalent hematological malignancy and is currently incurable. Although current treatment strategies, including chemotherapy, immunotherapy, and autologous stem cell transplantation can improve the survival of MM patients, many patients still experience recurrent-refractory disease. Hence, there is an urgent need to explore new therapeutic approaches for MM.

The structure and function of exosomes have been studied since their first discovery in the twentieth century. Exosomes are membranous vesicles that are constitutively released by almost all kinds of cells. They were first coined by Trams et al to describe the extracellular release of vesicles with 5' -nucleotide activity by normal cells and tumor cells [1]. Then in the late 1980s, this term was used to describe vesicles of endosomal origins released after the fusion of multivesicular bodies (MVBs) with cytoplasmic membranes during reticular cell differentiation [2]. Nowadays exosomes are proven to play key roles in regulating both physiological and pathological activities among cells. In addition to mediating local cell-to-cell communication by transferring proteins, lipids, and nucleic acids to recipient cells, exosomes can also induce the activation, proliferation, differentiation, and death of target cells. Some components of exosomes such as miRNAs and proteins that are specifically expressed in MM may be useful as therapeutic targets. Using their inhibitors or analogs to stabilize specific exosome expression levels in MM patients may decrease the carcinogenic effects or increase the tumor-suppressive effects of exosomes. Tumor-derived exosomes and their modified products can be developed into vaccines for anti-tumor immunity. Furthermore, natural nano structures of exosomes make them proper carriers to deliver target drugs.

Overview of exosomes

Exosomes are a kind of extracellular vesicles (EVs). On the basis of differences in biosynthesis and size, EVs are divided into three subgroups: microparticles derived from the shedding membrane, exosomes arising from MVBs, and EVs resulting from apoptosis. Microparticles (also known as microvesicles) are medium-sized vesicles, ranging from 200 to 1,000 nm; apoptotic bodies are larger (800-5,000 nm), whereas exosomes are smaller (30-150 nm) [3]. Exosomes are generated through endocytosis pathways in which the cell membrane sinks into the inner body to form early endosomes. Then early endosomes developed into late endosomes, which are transformed into polycystic bodies with a dynamic subcellular structure (MVB) [4]. MVBs are important protein transport and sorting centers of eukaryotic cells and are closely related to signal conduction, cytoplasmic division, gene silencing, autophagy, and virus budding. When MVBs fuse with lysosomes, the inner luminal vesicles undergo degradation and then fuse with the plasma membrane. Next, the inner luminal vesicles within sunk again, budding into granular vesicles known as exosomes [5], and then are released into the extracellular environment and body fluids (plasma, urine, saliva, ascites, amniotic fluid, lactic and cerebrospinal fluid) [6].

Exosomes can be secreted by almost all kinds of cells and act as signal presenters in the microenvironment. The exosome surface is rich in cholesterol, sphingomyelin, ceramide lipids and contains protein, mRNA, miRNA, and other biological information, which can be delivered to various recipient cells. There are several ways by which exosomes are taken up by recipient cells: (a) receptor-or lipiodraft-mediated endocytosis, (b) phagocytosis, (c) macropinocytosis, or (d) fusion with the plasma membrane of a target cell [7].

Influence of exosomes on MM

The BM microenvironment is closely associated with MM generation, progression, immunosuppression, and drug resistance. BM stromal cells (BMSCs) may play important roles in the BM microenvironment, but these roles have not been fully elucidated [Figure 1]. One study demonstrated a tumor-supportive role of BMSC-derived exosomes: compared with BMSC-derived exosomes in normal samples, BMSC-derived exosomes in MM expressed a lower level of miRNA-15a, which has been identified as a tumor-suppressive factor. In addition, BMSC-derived exosomes in MM expressed a higher level of fibronectin, indicating that they affect MM cell adhesion differentially [8]. Another study by Wang et al indicated that BMSC-derived exosomes can promote the proliferation, migration, and survival of MM cells, induce drug resistance to bortezomib, and influence several signaling pathways including c-Jun N-terminal kinase, TP38, TP53, and AKT, which are relevant to the survival of MM cells [9].

Accordingly, MM-derived exosomes influence the activities of various cells in the BM microenvironment by creating a pro-tumor environment for MM [Figure 2]. A study showed that miRNA-146a in MM-derived exosomes could be transmitted into BMSCs, resulting in the up-regulation of some specific cytokines and chemokines, such as CXCL1, IL-6, IL-8, IP10, MCP-1, and CCL-5, which leaded to the increased vitality and progression of MM cells. This study showed a positive feedback loop in which MM cells up-regulated the expression of miRNA-146a in BMSCs, resulting in more cytokine secretion, which in turn favored MM cell growth and migration [10]. A study of angiogenesis and immunosuppression, both in vivo and in vitro, demonstrated the presence of multiple angiogenic factors, such as angiogenin, basic fibroblast growth factor, vascular endothelial growth factor, and miRNA-135b, were closely associated with angiogenesis in MM [11]. Umezu et al also demonstrated that miRNA-135b from MM-derived exosomes accelerated HIF-1 transcriptional activity by inhibiting FIH-1; this HIF-FIH signaling pathway exerted an angiogenesis influence [12]. In addition, MM-derived exosomes can serve as a promoter for MM immunosuppression. Exosomes up-regulate nitric oxide synthase in myeloid-derived suppressor cells (MDSCs) and enhance their immunosuppression ability [13]. MM-derived exosomes can also modulate the survival and differentiation of osteoclasts by increasing CXCR4 expression and triggering the AKT pathway [14]. Stefania Raimondo et al also demonstrated that MM-derived exosomes were enriched of amphiregulin (AREG), and this exosomes-derived AREG can led to the activation of epidermal growth factor receptor ligands (EGFR) in preosteoclast, thus help to induce differentiation of osteoclasts [15]. Overall, exosomes serve as information communicators between cells and play a vital role in MM progression.

 Figure 1 

Effects of exosomes from BMSC in microenviroment on MM cells. BMSC-derived exosomes can increase vitality and progression of MM cells through cytokines and chemokines: IL-6, IPIO, MCP-1, CCL1 and downregulate miR15a; increase homing by upregulating fibronection, SDF1 and MCP-1; promote and resistance by increasing full-length caspase-8, caspase9, caspase3 and PARP. CCL1: chemokine ligand 1, IL6: interleukin 6, IL8: interleukin 8, IP10: interferon - inducible protein -10, MCP-1: monocyte chemotactic protein-1, CCL5: chemokine ligand 5, SDF1: stromal cell-derived factor 1, PRAP: poly ADP-ribose polymerase.

J Cancer Image (Click on the image to enlarge.)
 Figure 2 

Effects of exosomes from MM cells on different cells in microenvironment, thus induce a favorable microenvironment for MM growth. bFGF: b fibroblast growth factor; VEGF: vascular endothelial growth factor; CXCR4: cysteine X cysteine receptor 4; EGFR: epidermal growth factor receptor ligands.

J Cancer Image (Click on the image to enlarge.)

miRNA related potential treatment targets for MM in exosomes

Exosomes can be potential diagnostic biomarkers and facilitate the diagnosis and classification of diseases and contribute to the prediction of prognosis in cancer patients as well [16-19]. As an important component of exosomes, miRNAs vary in types and amounts among different exosomes and cells, and the abnormal expression of certain miRNAs is often associated with the clinical diagnosis. However, there are limited studies about miRNAs in MM therapy.

One important reason that studies of miRNAs in MM are limited is the lack of reliable and relatively simple technologies to separate and extracting specific miRNAs from samples. Another reason is that the therapeutic application of miRNAs is still under clinical investigations. The highly effective delivery of suitable miRNAs to MM cells and their uptake by the latter with no off-target effects remain challenging, hindering the development of an effective miRNA-based therapy. Nevertheless, the abnormal expression of certain miRNAs in MM-derived exosomes seems to be a treatment target in MM [Table 1].

As mentioned before, the high expression of miRNA-146a, promotes tumor progression through its involvement in the endogenous Notch pathway. The Notch pathway interacts with the NF-κB, JAK-STAT, and MAPK pathways, and they work together to regulate multiple gene transcriptions in MM progression. Therefore, DAPT, an inhibitor of endogenous Notch pathway, can inhibit the release of cytokines induced by miRNA-146a in MM [10]. miRNA-135b is expressed highly and exists stably in the hypoxic MM microenvironment, promoting endothelial vessel formation through the HIF-FIH signaling pathway. miRNA-135b may only be related to local area information transmission instead of cyclic plasma cells. Therefore, miRNA-135b may not be a suitable biomarker for MM diagnosis. However, its role in local tumor angiogenesis makes it a biomarker of angiogenesis in MM patients with locally relapsed disease, which inspires the exploration of specific blocking agents of miRNA-135b that may inhibit local angiogenesis [12].

miRNAs regulate gene expressions. Targeting the miRNA that act as tumor suppressors seems to be a promising miRNA-based treatment strategy. A recent study demonstrated that miRNA-34a over-expression in MM cells inhibited both cell proliferation and colony formation while increasing apoptosis in cancer stem cells in vitro [20]. Transient expression of miRNA-34a synthetic mimics or lentivirus-based miRNA-34a transduced into mice induced growth suppression and apoptosis in MM cells. Synthetic miRNA-34a downregulated the transcription and translation of BCL2, CDK6, and Notch 1. In addition, the anti-MM activity of miRNA-34a was found to result in no evidence of toxicity in mice, suggesting a favorable therapeutic index [21].

In a study by Leone, E. et al, significant inhibition of primary MM cells or of IL-6-dependent and -independent MM cell proliferation was triggered by miRNA-21 inhibitors. Meanwhile, transfection of miRNA-21 mimics increased the proliferation of MM cells, demonstrating the tumor-promoting potential of miRNA-21 in MM. Therefore, transient enforced expression or lentivirus-based constitutive expression of miRNA-21 inhibitors appears to be a promising treatment strategy for MM [22]. Morelli et al showed that anti-MM activity was induced by selectively targeting interferon regulatory factor 4 with synthetic miRNA-125b-5p mimics in vitro and in vivo. The fact that interferon regulatory factor 4 was inhibited, and its downstream effectors—c-MYC, CASPASE-10, and c-FLIP—were down-regulated as well, provided proof-of-concept that synthetic miRNA-125b-5p mimics are promising anti-MM agents [23]. Another study revealed a novel role of miRNA-137/197 in mediating MM cell apoptosis by targeting MCL-1. Lentivirus-based or formulated synthetic miRNA-137/197 exerted a therapeutic effect in preclinical models, which supported the suppression role of miRNA-137/197 in MM [24].

Upregulated miRNAs may be MM therapeutic targets by blocking their promoting effect on MM growth with appropriate inhibitors. Down-regulated miRNAs can be targeted using lentivirus-based or formulated synthetic mimics or other mimics. Nevertheless, one of the challenges in miRNA therapy is that mimics must be confirmed to have acceptable side effects or toxicities, which necessitates more clinical trials. In addition, more advanced technologies are needed for the mass production of mimics.

 Table 1 

Exosome-related therapy targets for MM patients

TargetProperty in exosomesSourceExpression patternFunctionRef.
miR-15amiRNABM-MSCsDown-regulatedInhibit MM cell proliferation[8]
miR-146amiRNABM-MSCsUp-regulatedStimulate the production of more cytokines that promote the growth of MM cells, including CXCL1, IL-6, IL-8, IP10, MCP-1, and CCL-5[10]
miR-135bmiRNAMM cellsUp-regulatedSuppress factor-inhibiting hypoxia inducible factor 1 (FIH-1) in endothelial cells directly[12]
miR-34amiRNAMM cancer stem cells (CSCs)Down-regulatedInhibit cell proliferation, colony formation, and increase CSC apoptosis in vitro[20]
miR-34amiRNAMM cellsDown-regulatedTrigger growth inhibition and apoptosis in MM cells[21]
miR-21miRNAMM cellsUp-regulatedMiR-21 inhibitors trigger significant growth inhibition of primary MM cells or IL-6-dependent/-independent MM cells[22]
miR-125b-5pmiRNAMM cellsDown-regulatedImpair MM cell growth and survival in vitro[23]
miR-137/197miRNAMM cellsDown-regulatedReduce MCL-1 protein expression, alter apoptosis-related gene expression, and induce apoptosis and inhibit viability, colony formation, and migration in MM cells[24]
HeparanaseProteinMM cellsUp-regulatedRegulate tumor metastasis, angiogenesis, and chemoresistance[29]
STT0001Chemically modified heparin----------------Inhibit myeloma growth in vivo effectively and cause changes within tumors that are consistent with the compound's ability to inhibit heparanase[30]
CeramideSphingolipid----------------Dose-dependently inhibit proliferation and promote apoptosis in human MM OPM2 cells and increase exosomal levels of tumor-suppressive miRNAs (miR-202, miR-16, miR-29b, and miR-15a)[32]

Protein related potential treatment targets for MM in exosomes

Allogenic exosomes have the potential to overcome one of the main challenges of cell-based therapies—immune response. They can provide a relatively stable environment for therapeutic agents and show the potential to be modified to enhance cell-specific homing, as well as to fuse with the plasma membranes of cells, making it possible for agents to enter the target cells directly [25]. The potential therapeutic role of proteins derived from exosomes in MM has been attractive. However, the unstable variety and content of proteins due to individual and organ tissue specificity have prevented the further study of exosomes-derived proteins. In addition, the protein may not be a suitable surrogate for EV quantity since each EV contains various amounts of proteins. Nevertheless, exosome-derived proteins of MM show significant value as biomarkers for diagnosis and prognosis. High expression of specific proteins in exosomes from different body fluids can be used to facilitate the diagnosis and predict the prognosis of a variety of diseases, such as lung cancer, pancreatic cancer, liver cancer, cholangiocarcinoma, gastric cancer, nervous system diseases, and genitourinary system diseases [26-27].

Currently, a protein named heparanase, which is delivered through the secretion of exosomes, is attracting the attention of many researchers. Released by tumor or host cells such as macrophages, heparanase can diffuse within the microenvironment and play a part in the functions of neighboring tumor cells by interacting with them and promoting the secretion of exosomes. It impacts exosome protein cargo by inducing it to express cytokines that are related to the development of tumors and the formation of blood vessels, such as syndecan-1, vascular endothelial growth factor, and hepatocyte growth factor at higher levels compared with heparenase-low expressing cells [28-29]. Studies have shown that compared with healthy donors, the expression of heparanase in MM patients is higher, indicating that heparanase is a therapeutic target in these patients [Table 1]. A study by Ritchie et al demonstrated that a heparanase inhibitor called SST0001 disrupted the MM tumor microenvironment and inhibited tumor growth [30]. Another study demonstrated that H1023, a monoclonal antibody, inhibited heparanase enzymatic activity [31]. The inhibitors of heparanase that are currently being evaluated in clinical trials are all modified heparins or heparin mimics; more types of highly specific inhibitors, such as monoclonal antibodies and small molecule chemical inhibitors, have yet to be exploited. Further studies are also needed to explore the exact composition and characteristics of proteins in MM-derived exosomes and to identify suitable regulators that react with proteins to make it possible for exosome-derived proteins to be utilized in clinical therapy.

Other exosome-associated treatment methods for MM

Apart from miRNAs and proteins, there are other exosome-associated treatment methods for MM [Table 1]. For instance, C6 ceramide, an exogenous ceramide supplement, was found to dose-dependently stimulate exosome secretion and elevate the exosome levels of some tumor-suppressive miRNAs, such as miRNA-202, miRNA-16, miRNA-29b, and miRNA-15a, thus increasing the apoptosis and inhibiting the proliferation of recipient MM cells, indicating that it is a target for MM treatment [32]. Exosomes also show anti-tumor immune effects. For example, a previous study confirmed that exosomes secreted by dendritic cells induced the inhibition of tumor growth in mice. In this study, the authors reported that the treatment efficacy of dendritic cells from the peripheral blood of stage III/IV non-small-cell lung cancer (NSCLC) and melanoma patients who did not undergo surgery was evaluated successfully in a phase I clinical trial, and no CD8+ T cells were detected in response [33].

According to a study by Xie et al, vaccines developed from exosomes were effective for MM. In their studies, exosomes from MM cells were used to stimulate anti-tumor immune responses and produce prophylactic immunity in MM cell lines [34-35]. A membrane protein named multiple myeloma special antigen-1, was specifically expressed in and correlated with MM. By taking advantage of its epitope, a vaccine called SLSLLTIYV, induced the obvious cytotoxic T lymphocyte response in vitro. MM special antigen-1-derived epitopes could combine with Dickkopf-1 to construct a multi-epitope peptide vaccine that substantially improved the survival rate compared with a single-epitope vaccine in a severely immune-deficient MM mouse model. This multi-epitope vaccine also greatly relieved the tumor burden and alleviated bone destruction, which will benefit MM patients in individualized therapy.

Exosomes as proper carriers to deliver target drugs

In addition to providing potential therapeutic targets, the natural nano structures of exosomes enable them excellent to be drug carriers and beneficial tools for tumor-targeted drug therapy. The surface of exosomes is a phospholipid bilayer mounted with a complex and special protein, which provides effective protection for loaded drugs within exosomes and helps these drugs to escape the capture by the reticuloendothelial system, extending their circulation time to combine with targets in vivo. More importantly, exosomes membranes can easily fuse with their counterparts in receptor cells, allowing the loaded drugs to be released into the cells directly. This natural structure of exosomes makes them perfect carriers for transporting drugs, such as gene drugs, anti-cancer drugs, and anti-inflammatory drugs [36-41]. According to a reported study, when the researchers developed a formulation of paclitaxel (PTX) -loaded exosomes with incorporated aminoethylanisamide-polyethylene glycol (AA-PEG) vector moiety in order to target the sigma receptor, which is overexpressed by lung cancer cells, the AA-PEG-vectorized exosomes loaded with PTX (AA-PEG-exoPTX) were found to possess a high loading capacity, strong ability to accumulate in lung cancer cells upon systemic administration, and also improved therapeutic outcomes. The combination of targeting ability with the biocompatibility of exosome-based drug formulations offers a novel delivery choice for anticancer therapy [42]. At present, there are several methods for loading “cargo” into exosomes: (a) transfection of exosome‑secreting cells [43], (b) chemical‑based exosome incorporation with exogenous cargoes [44], (c) electroporation [45] and alternative exosome‑loading techniques [46].

Exosome mimetics have similar sizes, surface morphologic features, and targeting abilities as exosomes. Jang et al discovered that chemotherapeutic drug-loaded nanovesicles, as exosome mimetics, inhibited tumor growth in vitro and in vivo, with no adverse effects [47]; Wu et al first reported the preparation for exosome-mimetic nanovesicles (NVs) from primary hepatocytes with almost 100 times the production yield compared with exosomes. Meanwhile, NVs were demonstrated to have both components and biofunctions similar to exosomes from primary hepatocytes [48]. These findings indicate that exosome mimetics, serving as drug carriers to replace exosomes, can effectively overcome two common issues with exosomes: the difficulties of mass production and the time-consuming nature of the purification process. Therefore, exosomes have many advantages over other existing delivery systems. In MM therapy, it may be possible to use exosomes or their mimics as carriers to load miRNA or protein inhibitors or mimics, since endogenous miRNAs can be encapsulated into exosomes to escape endonuclease degradation.

Conclusions and future perspective

Taken together, several abnormally expressed components in MM-derived exosomes, including miRNAs, proteins, and sphingolipids are potential targets for MM treatment. Utilizing the regulators of these components may have a tumor-suppressive effect. In addition, exosomes can be developed into vaccines for prophylactic immunity. The natural nano structure of exosomes makes them excellent carriers for drug delivery. However, when it comes to the future use of exosomes, there are still issues that need to be resolved. For components such as miRNAs, proteins, and sphingolipids, mass production of their mimics or regulators remains a major obstacle. Studies of exosome vaccines are still limited. Thus, more studies are needed to ensure that these treatments are effective and safe. Satisfactory efficacy and safety profiles have been demonstrated for exosomes and their mimics in other types of diseases, including NSCLC, type 1 diabetes mellitus, and colon cancer, but clinical trials in MM are still absent. Therefore, MM clinical trials are indispensable.

Abbreviations

MM: multiple myeloma; MVBs: multi-vesicle bodies; EVs: extracellular vesicles; BM: bone marrow; BMSCs: bone marrow stromal cells; MDSCs: myeloid-derived suppressor cells; AREG: amphiregulin; EGFR: epidermal growth factor receptor; NSCLC: non-small-cell lung cancer; PTX: paclitaxel; AA-PEG: aminoethylanisamide-polyethylene glycol; AA-PEG-exoPTX: AA-PEG-vectorized exosomes loaded with PTX; NVs: nanovesicles.

Acknowledgements

Funding

This work was supported by grants 81600163 and 81570201 from the National Natural Science Foundation of China (NSFC). M. J. Y. was supported in part by NIH/NCI R01 CA164346.

Authors' contributions

Mengzhen Li, Bing Xia and Yi Wang drafted the paper. M. James You and Yizhuo Zhang critically revised the paper. All authors approved the final manuscript and are responsible for the accuracy and integrity of all aspects of the manuscript.

Competing Interests

The authors have declared that no competing interest exists.

References

1. Trams EG, Lauter CJ, Salem N Jr. et al. Exofoliation of membrane ecto-enzymes in the form of micro-vesicles. Biochim Biophys Acta. 1981;645:63-70

2. Harding C, Heuser J, Stahl P. Receptor-mediated endocytosis of transferrin and recycling of the transferrin receptor in ratreticulocytes. J Cell Biol. 1983;97:329-39

3. He C, Zheng S, Luo Y. et al. Exosome Theranostics: Biology and Translational Medicine. Theranostics. 2018;8:237-255

4. Hessvik NP, Llorente A. Current knowledge on exosome biogenesis and release. Cell Mol Life Sci. 2018;75:193-208

5. Farooqi AA, Desai NN, Qureshi MZ. et al. Exosome biogenesis, bioactivities and functions as new delivery systems of natural compounds. Biotechnol Adv. 2018;36:328-334

6. Zhou J, Tan X, Tan Y. et al. Mesenchymal Stem Cell Derived Exosomes in Cancer Progression, Metastasis and Drug Delivery: A Comprehensive Review. J Cancer. 2018;9:3129-3137

7. Guo W, Gao Y, Li N. et al. Exosomes: New players in cancer (Review). Oncol Rep. 2017;38:665-675

8. Roccaro AM, Sacco A, Maiso P. et al. BM mesenchymal stromal cell-derived exosomes facilitate multiple myeloma progression. J Clin Invest. 2013;123:1542-55

9. Wang J, Hendrix A, Hernot S. et al. Bone marrow stromal cell-derived exosomes as communicators in drug resistance in multiple myeloma cells. Blood. 2014;124:555-66

10. De Veirman K, Wang J, Xu S. et al. Induction of miR-146a by multiple myeloma cells in mesenchymal stromal cells stimulates their pro-tumoral activity. Cancer Lett. 2016;377:17-24

11. Wang J, De Veirman K, Faict S. et al. Multiple myeloma exosomes establish a favourable bone marrow microenvironment with enhanced angiogenesis and immunosuppression. J Pathol. 2016;239:162-73

12. Umezu T, Tadokoro H, Azuma K. et al. Exosomal miR-135b shed from hypoxic multiple myeloma cells enhances angiogenesis by targeting factor-inhibiting HIF-1. Blood. 2014;124:3748-57

13. Wang J, De Veirman K, De Beule N. et al. The bone marrow microenvironment enhances multiple myeloma progression by exosome-mediated activation of myeloid-derived suppressor cells. Oncotarget. 2015;6:43992-4004

14. Raimondi L, De Luca A, Amodio N. et al. Involvement of multiple myeloma cell-derived exosomes in osteoclast differentiation. Oncotarget. 2015;6:13772-789

15. Raimondo S, Saieva L, Vicario E. et al. Multiple myeloma-derived exosomes are enriched of amphiregulin (AREG) and activate the epidermal growth factor pathway in the bone microenvironment leading to osteoclastogenesis. J Hematol Oncol. 2019;12:2

16. Sun Z, Shi K, Yang S. et al. Effect of exosomal miRNA on cancer biology and clinical applications. Mol Cancer. 2018;17:147

17. Jung SH, Lee SE, Lee M. et al. Circulating microRNA expressions can predict the outcome of lenalidomide plus low-dose dexamethasone treatment in patients with refractory/relapsed multiple myeloma. Haematologica. 2017;102:e456-e459

18. Hao M, Zang M, Zhao L. et al. Serum high expression of miR-214 and miR-135b as novel predictor for myeloma bone disease development and prognosis. Oncotarget. 2016;7:19589-600

19. Manier S, Liu CJ, Avet-Loiseau H. et al. Prognostic role of circulating exosomal miRNAs in multiple myeloma. Blood. 2017;129:2429-36

20. Wu S, He X, Li M. et al. MiRNA-34a overexpression inhibits multiple myeloma cancer stem cell growth in mice by suppressing TGIF2. Am J of Transl Res. 2016;8:5433-443

21. Di Martino MT, Leone E, Amodio N. et al. Synthetic miR-34a mimics as a novel therapeutic agent for multiple myeloma: in vitro and in vivo evidence. Clin Cancer Res. 2012;18:6260-70

22. Leone E, Morelli E, Di Martino MT. et al. Targeting miR-21 inhibits in vitro and in vivo multiple myeloma cell growth. Clin Cancer Res. 2013;19:2096-106

23. Morelli E, Leone E, Cantafio ME. et al. Selective targeting of IRF4 by synthetic microRNA-125b-5p mimics induces anti-multiple myeloma activity in vitro and in vivo. Leukemia. 2015;29:2173-83

24. Yang Y, Li F, Saha MN. et al. miR-137 and miR-197 Induce Apoptosis and Suppress Tumorigenicity by Targeting MCL-1 in Multiple Myeloma. Clin Cancer Res. 2015;21:2399-411

25. Gilligan KE, Dwyer RM. Engineering Exosomes for Cancer Therapy. Mol Sci. 2017:18 pii: E1122

26. Sandfeld-Paulsen B, Aggerholm-Pedersen N, Bæk R. et al. Exosomal proteins as prognostic biomarkers in non-small cell lung cancer. Mol Oncol. 2016;10:1595-602

27. Li W, Li C, Zhou T. et al. Role of exosomal proteins in cancer diagnosis. Mol Cancer. 2017;16:145

28. Sanderson RD, Elkin M, Rapraeger AC. et al. Heparanase regulation of cancer, autophagy and inflammation: new mechanisms and targets for therapy. FEBS J. 2017;284:42-55

29. Thompson CA, Purushothaman A, Ramani VC. et al. Heparanase regulates secretion, composition, and function of tumor cell-derived exosomes. J Biol Chem. 2013;288:10093-99

30. Ritchie JP, Ramani VC, Ren Y. et al. SST0001, a chemically modified heparin, inhibits myeloma growth and angiogenesis via disruption of the heparanase/syndecan-1 axis. Clin Cancer Res. 2011;17:1382-93

31. Bandari SK, Purushothaman A, Ramani VC. et al. Chemotherapy induces secretion of exosomes loaded with heparanase that degrades extracellular matrix and impacts tumor and host cell behavior. Matrix Biol. 2018;65:104-118

32. Cheng Q, Li X, Wang Y. et al. The ceramide pathway is involved in the survival, apoptosis and exosome functions of human multiple myeloma cells in vitro. Acta Pharmacol Sin. 2018;39:561-68

33. Lässer C. Exosomes in diagnostic and therapeutic applications: biomarker, vaccine and RNA interference delivery vehicle. Expert Opin Biol Ther. 2015;15:103-17

34. Xie Y, Bai O, Zhang H. et al. Membrane-bound HSP70-engineered myeloma cell-derived exosomes stimulate more efficient CD8(+) CTL- and NK-mediated antitumour immunity than exosomes released from heat-shocked tumour cells expressing cytoplasmic HSP70. J Cell Mol Med. 2010;14:2655-666

35. Xie Y, Bai O, Zhang H. et al. Tumor necrosis factor gene-engineered J558 tumor cell-released exosomes stimulate tumor antigen P1A-specific CD8+ CTL responses and antitumor immunity. Cancer Biother Radiopharm. 2010;25:21-8

36. Ohno S, Takanashi M, Sudo K. et al. Systemically injected exosomes targeted to EGFR deliver antitumor microRNA to breast cancer cells. Mol Ther. 2013;21:185-91

37. Pascucci L, Coccè V, Bonomi A. et al. Paclitaxel is incorporated by mesenchymal stromal cells and released in exosomes that inhibit in vitro tumor growth: a new approach for drug delivery. J Control Release. 2014;192:262-70

38. Wang B, Yao K, Huuskes BM. et al. Mesenchymal Stem Cells Deliver Exogenous MicroRNA-let7c via Exosomes to Attenuate Renal Fibrosis. Mol Ther. 2016;24:1290-301

39. O'Brien KP, Khan S, Gilligan KE. et al. Employing mesenchymal stem cells to support tumor-targeted delivery of extracellular vesicle (EV)-encapsulated microRNA-379. Oncogene. 2018;37:2137-2149

40. Saari H, Lázaro-Ibáñez E, Viitala T. et al. Microvesicle- and exosome-mediated drug delivery enhances the cytotoxicity of Paclitaxel in autologous prostate cancer cells. J Control Release. 2015;220:727-37

41. Jia G, Han Y, An Y. et al. NRP-1 targeted and cargo-loaded exosomes facilitate simultaneous imaging and therapy of glioma in vitro and in vivo. Biomaterials. 2018;178:302-316

42. Kim MS, Haney MJ, Zhao Y. et al. Engineering macrophage-derived exosomes for targeted paclitaxel delivery to pulmonary metastases: in vitro and in vivo evaluations. Nanomedicine. 2018;14:195-204

43. Bellavia D, Raimondo S, Calabrese G. et al. Interleukin 3- receptor targeted exosomes inhibit in vitro and in vivo Chronic Myelogenous Leukemia cell growth. Theranostics. 2017;7:1333-1345

44. Antimisiaris S, Mourtas S, Papadia K. Targeted si-RNA with liposomes and exosomes (extracellular vesicles): How to unlock the potential. Int J Pharm. 2017;525:293-312

45. Lunavat TR, Jang SC, Nilsson L. et al. RNAi delivery by exosome-mimetic nanovesicles - Implications for targeting c-Myc in cancer. Biomaterials. 2016;102:231-8

46. Liu Y, Li D, Liu Z. et al. Targeted exosome-mediated delivery of opioid receptor Mu siRNA for the treatment of morphine relapse. Sci Rep. 2015;5:17543

47. Jang SC, Kim OY, Yoon CM. et al. Bioinspired exosome-mimetic nanovesicles for targeted delivery of chemotherapeutics to malignant tumors. ACS Nano. 2013;7:7698-710

48. Wu JY, Ji AL, Wang ZX. et al. Exosome-Mimetic Nanovesicles from Hepatocytes promote hepatocyte proliferation in vitro and liver regeneration in vivo. Sci Rep. 2018;8:2471

Author contact

Corresponding address Corresponding authors: Yizhuo Zhang, phone number:18622221239; email: zhangyzhorg.cn and M. James You, phone number:001-7137451657; email: mjamesyouorg


Received 2018-11-24
Accepted 2019-8-12
Published 2019-10-15