Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2012
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
_version_ 1782282777760104448
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
work_keys_str_mv AT choidongsic quantitativeproteomicsofextracellularvesiclesderivedfromhumanprimaryandmetastaticcolorectalcancercells
AT choidoyoung quantitativeproteomicsofextracellularvesiclesderivedfromhumanprimaryandmetastaticcolorectalcancercells
AT hongboksil quantitativeproteomicsofextracellularvesiclesderivedfromhumanprimaryandmetastaticcolorectalcancercells
AT jangsuchul quantitativeproteomicsofextracellularvesiclesderivedfromhumanprimaryandmetastaticcolorectalcancercells
AT kimdaekyum quantitativeproteomicsofextracellularvesiclesderivedfromhumanprimaryandmetastaticcolorectalcancercells
AT leejaewook quantitativeproteomicsofextracellularvesiclesderivedfromhumanprimaryandmetastaticcolorectalcancercells
AT kimyoonkeun quantitativeproteomicsofextracellularvesiclesderivedfromhumanprimaryandmetastaticcolorectalcancercells
AT kimkwangpyo quantitativeproteomicsofextracellularvesiclesderivedfromhumanprimaryandmetastaticcolorectalcancercells
AT ghoyongsong quantitativeproteomicsofextracellularvesiclesderivedfromhumanprimaryandmetastaticcolorectalcancercells