Skip to main content
Top
Published in: Cancer and Metastasis Reviews 3/2016

01-09-2016 | NON-THEMATIC REVIEW

The roles and implications of exosomes in sarcoma

Authors: Li Min, Jacson Shen, Chongqi Tu, Francis Hornicek, Zhenfeng Duan

Published in: Cancer and Metastasis Reviews | Issue 3/2016

Login to get access

Abstract

Better diagnostic biomarkers and therapeutic options are still necessary for patients with sarcomas due to the current limitations of diagnosis and treatment. Exosomes are small extracellular membrane vesicles that are released by various cells and are found in most body fluids. Tumor-derived exosomes have been proven to mediate tumorigenesis, intercellular communication, microenvironment modulation, and metastasis in different cancers, including in sarcomas. Recently, exosomes have been considered as potential biomarkers for sarcoma diagnosis and prognosis, and as possible targets for sarcoma therapy. Moreover, due to their specific cell tropism and bioavailability, exosomes can also be engineered as vehicles for drug delivery. In this review, we discuss recent advances in the roles of tumor-derived exosomes in sarcoma and their potential clinical applications.
Literature
1.
go back to reference Riggi, N., et al. (2007). Sarcomas: genetics, signalling, and cellular origins. Part 1: the fellowship of TET. Journal of Pathology, 213(1), 4–20.PubMedCrossRef Riggi, N., et al. (2007). Sarcomas: genetics, signalling, and cellular origins. Part 1: the fellowship of TET. Journal of Pathology, 213(1), 4–20.PubMedCrossRef
2.
go back to reference Harwood, J. L., et al. (2015). Targeted chemotherapy in bone and soft-tissue sarcoma. The Orthopedic Clinics of North America, 46(4), 587–608.PubMedCrossRef Harwood, J. L., et al. (2015). Targeted chemotherapy in bone and soft-tissue sarcoma. The Orthopedic Clinics of North America, 46(4), 587–608.PubMedCrossRef
4.
go back to reference Bielack, S. S., et al. (2009). Second and subsequent recurrences of osteosarcoma: presentation, treatment, and outcomes of 249 consecutive cooperative osteosarcoma study group patients. Journal of Clinical Oncology, 27(4), 557–565.PubMedCrossRef Bielack, S. S., et al. (2009). Second and subsequent recurrences of osteosarcoma: presentation, treatment, and outcomes of 249 consecutive cooperative osteosarcoma study group patients. Journal of Clinical Oncology, 27(4), 557–565.PubMedCrossRef
5.
go back to reference Benjamin, R.S., et al. (2015). Chemotherapy for bone sarcomas in adults: the MD Anderson experience. American Society of Clinical Oncology Educational Book, p. e656-60. Benjamin, R.S., et al. (2015). Chemotherapy for bone sarcomas in adults: the MD Anderson experience. American Society of Clinical Oncology Educational Book, p. e656-60.
6.
go back to reference Yakkioui, Y., et al. (2014). Chordoma: the entity. Biochimica et Biophysica Acta, 1846(2), 655–669.PubMed Yakkioui, Y., et al. (2014). Chordoma: the entity. Biochimica et Biophysica Acta, 1846(2), 655–669.PubMed
7.
go back to reference Johnstone, R. M., et al. (1987). Vesicle formation during reticulocyte maturation. Association of plasma membrane activities with released vesicles (exosomes). Journal of Biological Chemistry, 262(19), 9412–9420.PubMed Johnstone, R. M., et al. (1987). Vesicle formation during reticulocyte maturation. Association of plasma membrane activities with released vesicles (exosomes). Journal of Biological Chemistry, 262(19), 9412–9420.PubMed
8.
go back to reference Rabinowits, G., et al. (2009). Exosomal microRNA: a diagnostic marker for lung cancer. Clinical Lung Cancer, 10(1), 42–46.PubMedCrossRef Rabinowits, G., et al. (2009). Exosomal microRNA: a diagnostic marker for lung cancer. Clinical Lung Cancer, 10(1), 42–46.PubMedCrossRef
9.
go back to reference Silva, J., et al. (2012). Analysis of exosome release and its prognostic value in human colorectal cancer. Genes, Chromosomes & Cancer, 51(4), 409–418.CrossRef Silva, J., et al. (2012). Analysis of exosome release and its prognostic value in human colorectal cancer. Genes, Chromosomes & Cancer, 51(4), 409–418.CrossRef
11.
12.
13.
go back to reference Ye, S. B., et al. (2014). Tumor-derived exosomes promote tumor progression and T-cell dysfunction through the regulation of enriched exosomal microRNAs in human nasopharyngeal carcinoma. Oncotarget, 5(14), 5439–5452.PubMedPubMedCentralCrossRef Ye, S. B., et al. (2014). Tumor-derived exosomes promote tumor progression and T-cell dysfunction through the regulation of enriched exosomal microRNAs in human nasopharyngeal carcinoma. Oncotarget, 5(14), 5439–5452.PubMedPubMedCentralCrossRef
14.
go back to reference Kim, M. S., et al. (2016). Development of exosome-encapsulated paclitaxel to overcome MDR in cancer cells. Nanomedicine, 12(3), 655–664.PubMed Kim, M. S., et al. (2016). Development of exosome-encapsulated paclitaxel to overcome MDR in cancer cells. Nanomedicine, 12(3), 655–664.PubMed
15.
go back to reference Rivoltini, L., et al. (2016). TNF-related apoptosis-inducing ligand (TRAIL)-armed exosomes deliver pro-apoptotic signals to tumor site. Clinical Cancer Research. Rivoltini, L., et al. (2016). TNF-related apoptosis-inducing ligand (TRAIL)-armed exosomes deliver pro-apoptotic signals to tumor site. Clinical Cancer Research.
16.
17.
go back to reference Cocucci, E., & Meldolesi, J. (2015). Ectosomes and exosomes: shedding the confusion between extracellular vesicles. Trends in Cell Biology, 25(6), 364–372.PubMedCrossRef Cocucci, E., & Meldolesi, J. (2015). Ectosomes and exosomes: shedding the confusion between extracellular vesicles. Trends in Cell Biology, 25(6), 364–372.PubMedCrossRef
18.
go back to reference Minciacchi, V. R., Freeman, M. R., & Di Vizio, D. (2015). Extracellular vesicles in cancer: exosomes, microvesicles and the emerging role of large oncosomes. Seminars in Cell and Developmental Biology, 40, 41–51.PubMedPubMedCentralCrossRef Minciacchi, V. R., Freeman, M. R., & Di Vizio, D. (2015). Extracellular vesicles in cancer: exosomes, microvesicles and the emerging role of large oncosomes. Seminars in Cell and Developmental Biology, 40, 41–51.PubMedPubMedCentralCrossRef
19.
go back to reference van der Pol, E., et al. (2012). Classification, functions, and clinical relevance of extracellular vesicles. Pharmacological Reviews, 64(3), 676–705.PubMedCrossRef van der Pol, E., et al. (2012). Classification, functions, and clinical relevance of extracellular vesicles. Pharmacological Reviews, 64(3), 676–705.PubMedCrossRef
20.
go back to reference Mathivanan, S., et al. (2012). ExoCarta 2012: database of exosomal proteins, RNA and lipids. Nucleic Acids Research, 40(Database issue), D1241–D1244.PubMedCrossRef Mathivanan, S., et al. (2012). ExoCarta 2012: database of exosomal proteins, RNA and lipids. Nucleic Acids Research, 40(Database issue), D1241–D1244.PubMedCrossRef
21.
go back to reference Baietti, M. F., et al. (2012). Syndecan-syntenin-ALIX regulates the biogenesis of exosomes. Nature Cell Biology, 14(7), 677–685.PubMedCrossRef Baietti, M. F., et al. (2012). Syndecan-syntenin-ALIX regulates the biogenesis of exosomes. Nature Cell Biology, 14(7), 677–685.PubMedCrossRef
22.
go back to reference Muralidharan-Chari, V., et al. (2009). ARF6-regulated shedding of tumor cell-derived plasma membrane microvesicles. Current Biology, 19(22), 1875–1885.PubMedPubMedCentralCrossRef Muralidharan-Chari, V., et al. (2009). ARF6-regulated shedding of tumor cell-derived plasma membrane microvesicles. Current Biology, 19(22), 1875–1885.PubMedPubMedCentralCrossRef
23.
go back to reference Akers, J. C., et al. (2013). Biogenesis of extracellular vesicles (EV): exosomes, microvesicles, retrovirus-like vesicles, and apoptotic bodies. Journal of Neuro-Oncology, 113(1), 1–11.PubMedCrossRef Akers, J. C., et al. (2013). Biogenesis of extracellular vesicles (EV): exosomes, microvesicles, retrovirus-like vesicles, and apoptotic bodies. Journal of Neuro-Oncology, 113(1), 1–11.PubMedCrossRef
24.
go back to reference Turiak, L., et al. (2011). Proteomic characterization of thymocyte-derived microvesicles and apoptotic bodies in BALB/c mice. Journal of Proteomics, 74(10), 2025–2033.PubMedCrossRef Turiak, L., et al. (2011). Proteomic characterization of thymocyte-derived microvesicles and apoptotic bodies in BALB/c mice. Journal of Proteomics, 74(10), 2025–2033.PubMedCrossRef
25.
go back to reference Minciacchi, V. R., et al. (2015). Large oncosomes contain distinct protein cargo and represent a separate functional class of tumor-derived extracellular vesicles. Oncotarget, 6(13), 11327–11341.PubMedPubMedCentralCrossRef Minciacchi, V. R., et al. (2015). Large oncosomes contain distinct protein cargo and represent a separate functional class of tumor-derived extracellular vesicles. Oncotarget, 6(13), 11327–11341.PubMedPubMedCentralCrossRef
26.
go back to reference Di Vizio, D., et al. (2012). Large oncosomes in human prostate cancer tissues and in the circulation of mice with metastatic disease. American Journal of Pathology, 181(5), 1573–1584.PubMedPubMedCentralCrossRef Di Vizio, D., et al. (2012). Large oncosomes in human prostate cancer tissues and in the circulation of mice with metastatic disease. American Journal of Pathology, 181(5), 1573–1584.PubMedPubMedCentralCrossRef
27.
go back to reference Ma, L., et al. (2015). Discovery of the migrasome, an organelle mediating release of cytoplasmic contents during cell migration. Cell Research, 25(1), 24–38.PubMedCrossRef Ma, L., et al. (2015). Discovery of the migrasome, an organelle mediating release of cytoplasmic contents during cell migration. Cell Research, 25(1), 24–38.PubMedCrossRef
28.
go back to reference Wright, P. K., et al. (2014). 17beta-estradiol regulates giant vesicle formation via estrogen receptor-alpha in human breast cancer cells. Oncotarget, 5(10), 3055–3065.PubMedPubMedCentralCrossRef Wright, P. K., et al. (2014). 17beta-estradiol regulates giant vesicle formation via estrogen receptor-alpha in human breast cancer cells. Oncotarget, 5(10), 3055–3065.PubMedPubMedCentralCrossRef
29.
go back to reference Colombo, M., Raposo, G., & Thery, C. (2014). Biogenesis, secretion, and intercellular interactions of exosomes and other extracellular vesicles. Annual Review of Cell and Developmental Biology, 30, 255–289.PubMedCrossRef Colombo, M., Raposo, G., & Thery, C. (2014). Biogenesis, secretion, and intercellular interactions of exosomes and other extracellular vesicles. Annual Review of Cell and Developmental Biology, 30, 255–289.PubMedCrossRef
30.
go back to reference Kowal, J., Tkach, M., & Thery, C. (2014). Biogenesis and secretion of exosomes. Current Opinion in Cell Biology, 29, 116–125.PubMedCrossRef Kowal, J., Tkach, M., & Thery, C. (2014). Biogenesis and secretion of exosomes. Current Opinion in Cell Biology, 29, 116–125.PubMedCrossRef
33.
go back to reference Takahashi, K., et al. (2014). Extracellular vesicle-mediated transfer of long non-coding RNA ROR modulates chemosensitivity in human hepatocellular cancer. FEBS Open Bio, 4, 458–467.PubMedPubMedCentralCrossRef Takahashi, K., et al. (2014). Extracellular vesicle-mediated transfer of long non-coding RNA ROR modulates chemosensitivity in human hepatocellular cancer. FEBS Open Bio, 4, 458–467.PubMedPubMedCentralCrossRef
34.
go back to reference Gusachenko, O. N., Zenkova, M. A., & Vlassov, V. V. (2013). Nucleic acids in exosomes: disease markers and intercellular communication molecules. Biochemistry (Mosc), 78(1), 1–7.CrossRef Gusachenko, O. N., Zenkova, M. A., & Vlassov, V. V. (2013). Nucleic acids in exosomes: disease markers and intercellular communication molecules. Biochemistry (Mosc), 78(1), 1–7.CrossRef
35.
go back to reference Gross, J. C., et al. (2012). Active Wnt proteins are secreted on exosomes. Nature Cell Biology, 14(10), 1036–1045.PubMedCrossRef Gross, J. C., et al. (2012). Active Wnt proteins are secreted on exosomes. Nature Cell Biology, 14(10), 1036–1045.PubMedCrossRef
36.
go back to reference Tsunemi, T., Hamada, K., & Krainc, D. (2014). ATP13A2/PARK9 regulates secretion of exosomes and alpha-synuclein. Journal of Neuroscience, 34(46), 15281–15287.PubMedPubMedCentralCrossRef Tsunemi, T., Hamada, K., & Krainc, D. (2014). ATP13A2/PARK9 regulates secretion of exosomes and alpha-synuclein. Journal of Neuroscience, 34(46), 15281–15287.PubMedPubMedCentralCrossRef
37.
go back to reference Wei, J. X., et al. (2015). Vps4A functions as a tumor suppressor by regulating the secretion and uptake of exosomal microRNAs in human hepatoma cells. Hepatology, 61(4), 1284–1294.PubMedPubMedCentralCrossRef Wei, J. X., et al. (2015). Vps4A functions as a tumor suppressor by regulating the secretion and uptake of exosomal microRNAs in human hepatoma cells. Hepatology, 61(4), 1284–1294.PubMedPubMedCentralCrossRef
38.
go back to reference Savina, A., et al. (2003). Exosome release is regulated by a calcium-dependent mechanism in K562 cells. Journal of Biological Chemistry, 278(22), 20083–20090.PubMedCrossRef Savina, A., et al. (2003). Exosome release is regulated by a calcium-dependent mechanism in K562 cells. Journal of Biological Chemistry, 278(22), 20083–20090.PubMedCrossRef
39.
go back to reference Li, J., et al. (2014). Beta-elemene against human lung cancer via up-regulation of P53 protein expression to promote the release of exosome. Lung Cancer, 86(2), 144–150.PubMedCrossRef Li, J., et al. (2014). Beta-elemene against human lung cancer via up-regulation of P53 protein expression to promote the release of exosome. Lung Cancer, 86(2), 144–150.PubMedCrossRef
40.
go back to reference Thompson, C. A., et al. (2013). Heparanase regulates secretion, composition, and function of tumor cell-derived exosomes. Journal of Biological Chemistry, 288(14), 10093–10099.PubMedPubMedCentralCrossRef Thompson, C. A., et al. (2013). Heparanase regulates secretion, composition, and function of tumor cell-derived exosomes. Journal of Biological Chemistry, 288(14), 10093–10099.PubMedPubMedCentralCrossRef
41.
go back to reference Tian, T., et al. (2010). Visualizing of the cellular uptake and intracellular trafficking of exosomes by live-cell microscopy. Journal of Cellular Biochemistry, 111(2), 488–496.PubMedCrossRef Tian, T., et al. (2010). Visualizing of the cellular uptake and intracellular trafficking of exosomes by live-cell microscopy. Journal of Cellular Biochemistry, 111(2), 488–496.PubMedCrossRef
42.
go back to reference Feng, D., et al. (2010). Cellular internalization of exosomes occurs through phagocytosis. Traffic, 11(5), 675–687.PubMedCrossRef Feng, D., et al. (2010). Cellular internalization of exosomes occurs through phagocytosis. Traffic, 11(5), 675–687.PubMedCrossRef
44.
go back to reference Szatanek, R., et al. (2015). Isolation of extracellular vesicles: determining the correct approach (review). International Journal of Molecular Medicine, 36(1), 11–17.PubMedPubMedCentral Szatanek, R., et al. (2015). Isolation of extracellular vesicles: determining the correct approach (review). International Journal of Molecular Medicine, 36(1), 11–17.PubMedPubMedCentral
45.
go back to reference Xu, R., et al. (2016). Extracellular vesicle isolation and characterization: toward clinical application. Journal of Clinical Investigation, 126(4), 1152–1162.PubMedCrossRef Xu, R., et al. (2016). Extracellular vesicle isolation and characterization: toward clinical application. Journal of Clinical Investigation, 126(4), 1152–1162.PubMedCrossRef
46.
go back to reference Abramowicz, A., Widlak P., Pietrowska, M. (2016). Proteomic analysis of exosomal cargo: the challenge of high purity vesicle isolation. Molecular Biosystems. Abramowicz, A., Widlak P., Pietrowska, M. (2016). Proteomic analysis of exosomal cargo: the challenge of high purity vesicle isolation. Molecular Biosystems.
47.
go back to reference Batrakova, E. V., & Kim, M. S. (2015). Using exosomes, naturally-equipped nanocarriers, for drug delivery. Journal of Controlled Release, 219, 396–405.PubMedCrossRef Batrakova, E. V., & Kim, M. S. (2015). Using exosomes, naturally-equipped nanocarriers, for drug delivery. Journal of Controlled Release, 219, 396–405.PubMedCrossRef
48.
go back to reference Zeringer, E., et al. (2015). Strategies for isolation of exosomes. Cold Spring Harbor Protocols, 2015(4), 319–323.PubMedCrossRef Zeringer, E., et al. (2015). Strategies for isolation of exosomes. Cold Spring Harbor Protocols, 2015(4), 319–323.PubMedCrossRef
49.
go back to reference Ko, J., Carpenter, E., & Issadore, D. (2016). Detection and isolation of circulating exosomes and microvesicles for cancer monitoring and diagnostics using micro-/nano-based devices. Analyst, 141(2), 450–460.PubMedCrossRef Ko, J., Carpenter, E., & Issadore, D. (2016). Detection and isolation of circulating exosomes and microvesicles for cancer monitoring and diagnostics using micro-/nano-based devices. Analyst, 141(2), 450–460.PubMedCrossRef
50.
go back to reference Erdbrugger, U., & Lannigan, J. (2016). Analytical challenges of extracellular vesicle detection: a comparison of different techniques. Cytometry. Part A, 89(2), 123–134.CrossRef Erdbrugger, U., & Lannigan, J. (2016). Analytical challenges of extracellular vesicle detection: a comparison of different techniques. Cytometry. Part A, 89(2), 123–134.CrossRef
51.
go back to reference Pope, S. M. & Lasser, C. (2013). Toxoplasma gondii infection of fibroblasts causes the production of exosome-like vesicles containing a unique array of mRNA and miRNA transcripts compared to serum starvation. Journal of Extracellular Vesicles, 2. Pope, S. M. & Lasser, C. (2013). Toxoplasma gondii infection of fibroblasts causes the production of exosome-like vesicles containing a unique array of mRNA and miRNA transcripts compared to serum starvation. Journal of Extracellular Vesicles, 2.
52.
go back to reference Jorgensen, M. M., Baek, R., & Varming, K. (2015). Potentials and capabilities of the extracellular vesicle (EV) array. Journal of Extracellular Vesicles, 4, 26048.PubMedCrossRef Jorgensen, M. M., Baek, R., & Varming, K. (2015). Potentials and capabilities of the extracellular vesicle (EV) array. Journal of Extracellular Vesicles, 4, 26048.PubMedCrossRef
53.
go back to reference Vlassov, A. V., et al. (2012). Exosomes: current knowledge of their composition, biological functions, and diagnostic and therapeutic potentials. Biochimica et Biophysica Acta, 1820(7), 940–948.PubMedCrossRef Vlassov, A. V., et al. (2012). Exosomes: current knowledge of their composition, biological functions, and diagnostic and therapeutic potentials. Biochimica et Biophysica Acta, 1820(7), 940–948.PubMedCrossRef
54.
go back to reference Liang, B., et al. (2013). Characterization and proteomic analysis of ovarian cancer-derived exosomes. Journal of Proteomics, 80, 171–182.PubMedCrossRef Liang, B., et al. (2013). Characterization and proteomic analysis of ovarian cancer-derived exosomes. Journal of Proteomics, 80, 171–182.PubMedCrossRef
55.
go back to reference Shimbo, K., et al. (2014). Exosome-formed synthetic microRNA-143 is transferred to osteosarcoma cells and inhibits their migration. Biochemical and Biophysical Research Communications, 445(2), 381–387.PubMedCrossRef Shimbo, K., et al. (2014). Exosome-formed synthetic microRNA-143 is transferred to osteosarcoma cells and inhibits their migration. Biochemical and Biophysical Research Communications, 445(2), 381–387.PubMedCrossRef
56.
go back to reference Ventura, S., et al. (2015). CD99 regulates neural differentiation of Ewing sarcoma cells through miR-34a-Notch-mediated control of NF-kappaB signaling. Oncogene. Ventura, S., et al. (2015). CD99 regulates neural differentiation of Ewing sarcoma cells through miR-34a-Notch-mediated control of NF-kappaB signaling. Oncogene.
57.
go back to reference Zeelenberg, I. S., et al. (2008). Targeting tumor antigens to secreted membrane vesicles in vivo induces efficient antitumor immune responses. Cancer Research, 68(4), 1228–1235.PubMedCrossRef Zeelenberg, I. S., et al. (2008). Targeting tumor antigens to secreted membrane vesicles in vivo induces efficient antitumor immune responses. Cancer Research, 68(4), 1228–1235.PubMedCrossRef
58.
go back to reference Zeelenberg, I. S., et al. (2011). Antigen localization controls T cell-mediated tumor immunity. The Journal of Immunology, 187(3), 1281–1288.PubMedCrossRef Zeelenberg, I. S., et al. (2011). Antigen localization controls T cell-mediated tumor immunity. The Journal of Immunology, 187(3), 1281–1288.PubMedCrossRef
59.
go back to reference Toda, Y., et al. (2015). Effective internalization of U251-MG-secreted exosomes into cancer cells and characterization of their lipid components. Biochemical and Biophysical Research Communications, 456(3), 768–773.PubMedCrossRef Toda, Y., et al. (2015). Effective internalization of U251-MG-secreted exosomes into cancer cells and characterization of their lipid components. Biochemical and Biophysical Research Communications, 456(3), 768–773.PubMedCrossRef
60.
go back to reference Mao, L., et al. (2016). Enterovirus 71 transmission by exosomes establishes a productive infection in human neuroblastoma cells. Virus Genes, 52(2), 189–194.PubMedCrossRef Mao, L., et al. (2016). Enterovirus 71 transmission by exosomes establishes a productive infection in human neuroblastoma cells. Virus Genes, 52(2), 189–194.PubMedCrossRef
61.
go back to reference Atay, S., et al. (2014). Oncogenic KIT-containing exosomes increase gastrointestinal stromal tumor cell invasion. Proceedings of the National Academy of Sciences of the United States of America, 111(2), 711–716.PubMedCrossRef Atay, S., et al. (2014). Oncogenic KIT-containing exosomes increase gastrointestinal stromal tumor cell invasion. Proceedings of the National Academy of Sciences of the United States of America, 111(2), 711–716.PubMedCrossRef
62.
go back to reference Tsuno, H., et al. (2016). Effects of methotrexate and salazosulfapyridine on protein profiles of exosomes derived from a human synovial sarcoma cell line of SW982. Proteomics Clinical Applications, 10(2), 164–171.PubMedCrossRef Tsuno, H., et al. (2016). Effects of methotrexate and salazosulfapyridine on protein profiles of exosomes derived from a human synovial sarcoma cell line of SW982. Proteomics Clinical Applications, 10(2), 164–171.PubMedCrossRef
63.
go back to reference Sommer, G., et al. (2003). Gastrointestinal stromal tumors in a mouse model by targeted mutation of the kit receptor tyrosine kinase. Proceedings of the National Academy of Sciences of the United States of America, 100(11), 6706–6711.PubMedPubMedCentralCrossRef Sommer, G., et al. (2003). Gastrointestinal stromal tumors in a mouse model by targeted mutation of the kit receptor tyrosine kinase. Proceedings of the National Academy of Sciences of the United States of America, 100(11), 6706–6711.PubMedPubMedCentralCrossRef
64.
go back to reference Rubin, B. P., et al. (2005). A knock-in mouse model of gastrointestinal stromal tumor harboring kit K641E. Cancer Research, 65(15), 6631–6639.PubMedCrossRef Rubin, B. P., et al. (2005). A knock-in mouse model of gastrointestinal stromal tumor harboring kit K641E. Cancer Research, 65(15), 6631–6639.PubMedCrossRef
65.
go back to reference Saleem, S. N., & Abdel-Mageed, A. B. (2015). Tumor-derived exosomes in oncogenic reprogramming and cancer progression. Cellular and Molecular Life Sciences, 72(1), 1–10.PubMedCrossRef Saleem, S. N., & Abdel-Mageed, A. B. (2015). Tumor-derived exosomes in oncogenic reprogramming and cancer progression. Cellular and Molecular Life Sciences, 72(1), 1–10.PubMedCrossRef
66.
go back to reference Endo-Munoz, L., et al. (2015). Progression of osteosarcoma from a non-metastatic to a metastatic phenotype is causally associated with activation of an autocrine and paracrine uPA Axis. PLoS One, 10(8), e0133592.PubMedPubMedCentralCrossRef Endo-Munoz, L., et al. (2015). Progression of osteosarcoma from a non-metastatic to a metastatic phenotype is causally associated with activation of an autocrine and paracrine uPA Axis. PLoS One, 10(8), e0133592.PubMedPubMedCentralCrossRef
67.
go back to reference Hakulinen, J., et al. (2008). Secretion of active membrane type 1 matrix metalloproteinase (MMP-14) into extracellular space in microvesicular exosomes. Journal of Cellular Biochemistry, 105(5), 1211–1218.PubMedCrossRef Hakulinen, J., et al. (2008). Secretion of active membrane type 1 matrix metalloproteinase (MMP-14) into extracellular space in microvesicular exosomes. Journal of Cellular Biochemistry, 105(5), 1211–1218.PubMedCrossRef
69.
go back to reference Miller, I. V., et al. (2013). First identification of Ewing’s sarcoma-derived extracellular vesicles and exploration of their biological and potential diagnostic implications. Biology of the Cell, 105(7), 289–303.PubMedCrossRef Miller, I. V., et al. (2013). First identification of Ewing’s sarcoma-derived extracellular vesicles and exploration of their biological and potential diagnostic implications. Biology of the Cell, 105(7), 289–303.PubMedCrossRef
70.
go back to reference Remacle, A., Murphy, G., & Roghi, C. (2003). Membrane type I-matrix metalloproteinase (MT1-MMP) is internalised by two different pathways and is recycled to the cell surface. Journal of Cell Science, 116(Pt 19), 3905–3916.PubMedCrossRef Remacle, A., Murphy, G., & Roghi, C. (2003). Membrane type I-matrix metalloproteinase (MT1-MMP) is internalised by two different pathways and is recycled to the cell surface. Journal of Cell Science, 116(Pt 19), 3905–3916.PubMedCrossRef
71.
go back to reference Thery, C., Zitvogel, L., & Amigorena, S. (2002). Exosomes: composition, biogenesis and function. Nature Reviews Immunology, 2(8), 569–579.PubMed Thery, C., Zitvogel, L., & Amigorena, S. (2002). Exosomes: composition, biogenesis and function. Nature Reviews Immunology, 2(8), 569–579.PubMed
72.
go back to reference Taylor, D. D., & Gercel-Taylor, C. (2008). MicroRNA signatures of tumor-derived exosomes as diagnostic biomarkers of ovarian cancer. Gynecologic Oncology, 110(1), 13–21.PubMedCrossRef Taylor, D. D., & Gercel-Taylor, C. (2008). MicroRNA signatures of tumor-derived exosomes as diagnostic biomarkers of ovarian cancer. Gynecologic Oncology, 110(1), 13–21.PubMedCrossRef
73.
go back to reference Liao, J., et al. (2016). Exosome-shuttling microRNA-21 promotes cell migration and invasion-targeting PDCD4 in esophageal cancer. International Journal of Oncology, 48(6), 2567–2579.PubMed Liao, J., et al. (2016). Exosome-shuttling microRNA-21 promotes cell migration and invasion-targeting PDCD4 in esophageal cancer. International Journal of Oncology, 48(6), 2567–2579.PubMed
74.
go back to reference Meng, X., et al. (2016). Diagnostic and prognostic relevance of circulating exosomal miR-373, miR-200a, miR-200b and miR-200c in patients with epithelial ovarian cancer. Oncotarget, 7(13), 16923–16935.PubMedPubMedCentral Meng, X., et al. (2016). Diagnostic and prognostic relevance of circulating exosomal miR-373, miR-200a, miR-200b and miR-200c in patients with epithelial ovarian cancer. Oncotarget, 7(13), 16923–16935.PubMedPubMedCentral
75.
go back to reference Munagala, R., Aqil, F., Gupta, R.C. (2016). Exosomal miRNAs as biomarkers of recurrent lung cancer. Tumour Biology. Munagala, R., Aqil, F., Gupta, R.C. (2016). Exosomal miRNAs as biomarkers of recurrent lung cancer. Tumour Biology.
76.
go back to reference Berrondo, C., et al. (2016). Expression of the long non-coding RNA HOTAIR correlates with disease progression in bladder cancer and is contained in bladder cancer patient urinary exosomes. PLoS One, 11(1), e0147236.PubMedPubMedCentralCrossRef Berrondo, C., et al. (2016). Expression of the long non-coding RNA HOTAIR correlates with disease progression in bladder cancer and is contained in bladder cancer patient urinary exosomes. PLoS One, 11(1), e0147236.PubMedPubMedCentralCrossRef
77.
go back to reference Ruiz-Martinez, M., et al. (2016). YKT6 expression, exosome release, and survival in non-small cell lung cancer. Oncotarget. Ruiz-Martinez, M., et al. (2016). YKT6 expression, exosome release, and survival in non-small cell lung cancer. Oncotarget.
78.
go back to reference Rodriguez, M., et al. (2015). Exosomes enriched in stemness/metastatic-related mRNAS promote oncogenic potential in breast cancer. Oncotarget, 6(38), 40575–40587.PubMedPubMedCentral Rodriguez, M., et al. (2015). Exosomes enriched in stemness/metastatic-related mRNAS promote oncogenic potential in breast cancer. Oncotarget, 6(38), 40575–40587.PubMedPubMedCentral
79.
go back to reference van den Boorn, J. G., et al. (2013). Exosomes as nucleic acid nanocarriers. Advanced Drug Delivery Reviews, 65(3), 331–335.PubMedCrossRef van den Boorn, J. G., et al. (2013). Exosomes as nucleic acid nanocarriers. Advanced Drug Delivery Reviews, 65(3), 331–335.PubMedCrossRef
80.
go back to reference Hood, J. L., San, R. S., & Wickline, S. A. (2011). Exosomes released by melanoma cells prepare sentinel lymph nodes for tumor metastasis. Cancer Research, 71(11), 3792–3801.PubMedCrossRef Hood, J. L., San, R. S., & Wickline, S. A. (2011). Exosomes released by melanoma cells prepare sentinel lymph nodes for tumor metastasis. Cancer Research, 71(11), 3792–3801.PubMedCrossRef
81.
go back to reference Alvarez-Erviti, L., et al. (2011). Delivery of siRNA to the mouse brain by systemic injection of targeted exosomes. Nature Biotechnology, 29(4), 341–345.PubMedCrossRef Alvarez-Erviti, L., et al. (2011). Delivery of siRNA to the mouse brain by systemic injection of targeted exosomes. Nature Biotechnology, 29(4), 341–345.PubMedCrossRef
82.
go back to reference Sun, D., et al. (2010). A novel nanoparticle drug delivery system: the anti-inflammatory activity of curcumin is enhanced when encapsulated in exosomes. Molecular Therapy, 18(9), 1606–1614.PubMedPubMedCentralCrossRef Sun, D., et al. (2010). A novel nanoparticle drug delivery system: the anti-inflammatory activity of curcumin is enhanced when encapsulated in exosomes. Molecular Therapy, 18(9), 1606–1614.PubMedPubMedCentralCrossRef
83.
go back to reference Zhuang, X., et al. (2011). Treatment of brain inflammatory diseases by delivering exosome encapsulated anti-inflammatory drugs from the nasal region to the brain. Molecular Therapy, 19(10), 1769–1779.PubMedPubMedCentralCrossRef Zhuang, X., et al. (2011). Treatment of brain inflammatory diseases by delivering exosome encapsulated anti-inflammatory drugs from the nasal region to the brain. Molecular Therapy, 19(10), 1769–1779.PubMedPubMedCentralCrossRef
84.
go back to reference Wahlgren, J., et al. (2012). Plasma exosomes can deliver exogenous short interfering RNA to monocytes and lymphocytes. Nucleic Acids Research, 40(17), e130.PubMedPubMedCentralCrossRef Wahlgren, J., et al. (2012). Plasma exosomes can deliver exogenous short interfering RNA to monocytes and lymphocytes. Nucleic Acids Research, 40(17), e130.PubMedPubMedCentralCrossRef
85.
go back to reference Katsuda, T., et al. (2013). The therapeutic potential of mesenchymal stem cell-derived extracellular vesicles. Proteomics, 13(10-11), 1637–1653.PubMedCrossRef Katsuda, T., et al. (2013). The therapeutic potential of mesenchymal stem cell-derived extracellular vesicles. Proteomics, 13(10-11), 1637–1653.PubMedCrossRef
86.
go back to reference Fang, Y., et al. (2015). Expression and clinical significance of cyclooxygenase-2 and microRNA-143 in osteosarcoma. Experimental and Therapeutic Medicine, 9(6), 2374–2378.PubMedPubMedCentral Fang, Y., et al. (2015). Expression and clinical significance of cyclooxygenase-2 and microRNA-143 in osteosarcoma. Experimental and Therapeutic Medicine, 9(6), 2374–2378.PubMedPubMedCentral
87.
go back to reference Zhou, J., et al. (2015). microRNA-143 is associated with the survival of ALDH1+CD133+ osteosarcoma cells and the chemoresistance of osteosarcoma. Experimental Biology and Medicine (Maywood, N.J.), 240(7), 867–875.CrossRef Zhou, J., et al. (2015). microRNA-143 is associated with the survival of ALDH1+CD133+ osteosarcoma cells and the chemoresistance of osteosarcoma. Experimental Biology and Medicine (Maywood, N.J.), 240(7), 867–875.CrossRef
88.
go back to reference Arroyo, J. D., et al. (2011). Argonaute2 complexes carry a population of circulating microRNAs independent of vesicles in human plasma. Proceedings of the National Academy of Sciences of the United States of America, 108(12), 5003–5008.PubMedPubMedCentralCrossRef Arroyo, J. D., et al. (2011). Argonaute2 complexes carry a population of circulating microRNAs independent of vesicles in human plasma. Proceedings of the National Academy of Sciences of the United States of America, 108(12), 5003–5008.PubMedPubMedCentralCrossRef
Metadata
Title
The roles and implications of exosomes in sarcoma
Authors
Li Min
Jacson Shen
Chongqi Tu
Francis Hornicek
Zhenfeng Duan
Publication date
01-09-2016
Publisher
Springer US
Published in
Cancer and Metastasis Reviews / Issue 3/2016
Print ISSN: 0167-7659
Electronic ISSN: 1573-7233
DOI
https://doi.org/10.1007/s10555-016-9630-4

Other articles of this Issue 3/2016

Cancer and Metastasis Reviews 3/2016 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine