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Quantitative proteomics of extracellular vesicles derived from human primary and metastatic colorectal cancer cells
Cancer cells actively release extracellular vesicles (EVs), including exosomes and microvesicles, into surrounding tissues. These EVs play pleiotropic roles in cancer progression and metastasis, including invasion, angiogenesis, and immune modulation. However, the proteomic differences between prima...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Co-Action Publishing
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3760640/ https://www.ncbi.nlm.nih.gov/pubmed/24009881 http://dx.doi.org/10.3402/jev.v1i0.18704 |
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author | Choi, Dong-Sic Choi, Do-Young Hong, Bok Sil Jang, Su Chul Kim, Dae-Kyum Lee, Jaewook Kim, Yoon-Keun Kim, Kwang Pyo Gho, Yong Song |
author_facet | Choi, Dong-Sic Choi, Do-Young Hong, Bok Sil Jang, Su Chul Kim, Dae-Kyum Lee, Jaewook Kim, Yoon-Keun Kim, Kwang Pyo Gho, Yong Song |
author_sort | Choi, Dong-Sic |
collection | PubMed |
description | Cancer cells actively release extracellular vesicles (EVs), including exosomes and microvesicles, into surrounding tissues. These EVs play pleiotropic roles in cancer progression and metastasis, including invasion, angiogenesis, and immune modulation. However, the proteomic differences between primary and metastatic cancer cell-derived EVs remain unclear. Here, we conducted comparative proteomic analysis between EVs derived from human primary colorectal cancer cells (SW480) and their metastatic derivatives (SW620). Using label-free quantitation, we identified 803 and 787 proteins in SW480 EVs and SW620 EVs, respectively. Based on comparison between the estimated abundance of EV proteins, we identified 368 SW480 EV-enriched and 359 SW620 EV-enriched proteins. SW480 EV-enriched proteins played a role in cell adhesion, but SW620 EV-enriched proteins were associated with cancer progression and functioned as diagnostic indicators of metastatic cancer; they were overexpressed in metastatic colorectal cancer and played roles in multidrug resistance. As the first proteomic analysis comparing primary and metastatic cancer-derived EVs, this study increases our understanding of the pathological function of EVs in the metastatic process and provides useful biomarkers for cancer metastasis. |
format | Online Article Text |
id | pubmed-3760640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Co-Action Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-37606402013-09-04 Quantitative proteomics of extracellular vesicles derived from human primary and metastatic colorectal cancer cells Choi, Dong-Sic Choi, Do-Young Hong, Bok Sil Jang, Su Chul Kim, Dae-Kyum Lee, Jaewook Kim, Yoon-Keun Kim, Kwang Pyo Gho, Yong Song J Extracell Vesicles Original Research Article Cancer cells actively release extracellular vesicles (EVs), including exosomes and microvesicles, into surrounding tissues. These EVs play pleiotropic roles in cancer progression and metastasis, including invasion, angiogenesis, and immune modulation. However, the proteomic differences between primary and metastatic cancer cell-derived EVs remain unclear. Here, we conducted comparative proteomic analysis between EVs derived from human primary colorectal cancer cells (SW480) and their metastatic derivatives (SW620). Using label-free quantitation, we identified 803 and 787 proteins in SW480 EVs and SW620 EVs, respectively. Based on comparison between the estimated abundance of EV proteins, we identified 368 SW480 EV-enriched and 359 SW620 EV-enriched proteins. SW480 EV-enriched proteins played a role in cell adhesion, but SW620 EV-enriched proteins were associated with cancer progression and functioned as diagnostic indicators of metastatic cancer; they were overexpressed in metastatic colorectal cancer and played roles in multidrug resistance. As the first proteomic analysis comparing primary and metastatic cancer-derived EVs, this study increases our understanding of the pathological function of EVs in the metastatic process and provides useful biomarkers for cancer metastasis. Co-Action Publishing 2012-09-11 /pmc/articles/PMC3760640/ /pubmed/24009881 http://dx.doi.org/10.3402/jev.v1i0.18704 Text en © 2012 Dong-Sic Choi et al. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Article Choi, Dong-Sic Choi, Do-Young Hong, Bok Sil Jang, Su Chul Kim, Dae-Kyum Lee, Jaewook Kim, Yoon-Keun Kim, Kwang Pyo Gho, Yong Song Quantitative proteomics of extracellular vesicles derived from human primary and metastatic colorectal cancer cells |
title | Quantitative proteomics of extracellular vesicles derived from human primary and metastatic colorectal cancer cells |
title_full | Quantitative proteomics of extracellular vesicles derived from human primary and metastatic colorectal cancer cells |
title_fullStr | Quantitative proteomics of extracellular vesicles derived from human primary and metastatic colorectal cancer cells |
title_full_unstemmed | Quantitative proteomics of extracellular vesicles derived from human primary and metastatic colorectal cancer cells |
title_short | Quantitative proteomics of extracellular vesicles derived from human primary and metastatic colorectal cancer cells |
title_sort | quantitative proteomics of extracellular vesicles derived from human primary and metastatic colorectal cancer cells |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3760640/ https://www.ncbi.nlm.nih.gov/pubmed/24009881 http://dx.doi.org/10.3402/jev.v1i0.18704 |
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