Proteomic analysis of microvesicles derived from human colorectal cancer ascites

The presence of malignant ascites in the peritoneal cavity is a poor prognostic indicator of low survival rate. Various cancer cells, including those of colorectal cancer (CRC), release microvesicles (exosomes) into surrounding tissues and peripheral circulation including malignant ascites. Although...

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Published inProteomics (Weinheim) Vol. 11; no. 13; pp. 2745 - 2751
Main Authors Choi, Dong-Sic, Park, Jung Ok, Jang, Su Chul, Yoon, Yae Jin, Jung, Jin Woo, Choi, Do-Young, Kim, Jung-Wook, Kang, Ji Seon, Park, Jaesung, Hwang, Daehee, Lee, Kyung-Hee, Park, Sang-Hyun, Kim, Yoon-Keun, Desiderio, Dominic M., Kim, Kwang Pyo, Gho, Yong Song
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 01.07.2011
WILEY‐VCH Verlag
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ISSN1615-9853
1615-9861
1862-8346
1615-9861
DOI10.1002/pmic.201100022

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Summary:The presence of malignant ascites in the peritoneal cavity is a poor prognostic indicator of low survival rate. Various cancer cells, including those of colorectal cancer (CRC), release microvesicles (exosomes) into surrounding tissues and peripheral circulation including malignant ascites. Although recent progress has revealed that microvesicles play multiple roles in tumor progression, the protein composition and the pathological function of malignant ascites‐derived microvesicles are still unknown. Here, we report the first global proteomic analyses of highly purified microvesicles derived from human CRC ascites. With 1‐D SDS‐PAGE and nano‐LC‐MS/MS analyses, we identified a total of 846 microvesicular proteins from ascites of three CRC patients with high confidence; 384 proteins were identified in at least two patients. We identified proteins that might function in tumor progression via disruption of epithelial polarity, migration, invasion, tumor growth, immune modulation, and angiogenesis. Furthermore, we identified several potential diagnostic markers of CRC including colon‐specific surface antigens. Our proteomic analyses will help to elucidate diverse functions of microvesicles in cancer progression and will aid in the development of novel diagnostic tools for CRC.
Bibliography:National R&D Program for Cancer Control, Ministry of Health & Welfare, Republic of Korea - No. 0820220
Mid-career Researcher Program through NRF
Korea Science and Engineering Foundation (KOSEF) NCRC
istex:C0F71339201BE4823A3DF26B2008E80C9CF75436
ark:/67375/WNG-NW56BCNL-T
National Research Foundation of Korea
ArticleID:PMIC201100022
WCU (World Class University)
Korea government (MEST) - No. 2010-0028447
MEST - No. 2009-0080709; No. 2010-0017496
Ministry of Education, Science and Technology - No. R33-10128
These authors contributed equally to this work.
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ISSN:1615-9853
1615-9861
1862-8346
1615-9861
DOI:10.1002/pmic.201100022