A catalogue of proteins released by colorectal cancer cells in vitro as an alternative source for biomarker discovery

被引:33
作者
Diehl, Hanna C.
Stuehler, Kai
Klein-Scory, Susanne
Volmer, Martin W.
Schoeneck, Anna
Bieling, Cornelia
Schmiegel, Wolff
Meyer, Helmut E.
Schwarte-Waldhoff, Irmgard
机构
[1] Ruhr Univ Bochum, IMBL, Dept Internal Med, Knappschaftskrankenhaus, D-44892 Bochum, Germany
[2] Ruhr Univ Bochum, Me dProteome Ctr, D-4630 Bochum, Germany
[3] Ruhr Univ Bochum, Klinikum Bergmannsheil, Dept Gastroenterol & Hepatol, D-4630 Bochum, Germany
关键词
colon cancer; exosome; kallikrein-6; secretome; soluble E-cadherin;
D O I
10.1002/prca.200600491
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
improved methods for the early diagnosis of colorectal cancer by way of sensitive and specific tumour markers are highly desirable. Therefore, efficient strategies for biomarker discovery are urgently needed. Here we present an approach that is based on the direct experimental access to proteins released by SW620 human colorectal cancer cells in vitro. A 2-D map and a catalogue of this subproteome - here termed the secretome - were established comprising more than 320 identified proteins which translate into approximately 220 distinct genes. As the majority of the secretome constituents were nominally cellular proteins, we directly compared the secretome and the total proteome by 2-D-DIGE analysis. We provide evidence that unspecific release through cell death, classical secretion, ectodomain shedding, and exosomal release contribute to the secretome in vitro, presumably reflecting the mechanisms in vivo which lead to the occurrence of tumour-specific proteins in the circulation. These data together with the fact that the SW620 secretome catalogue, as presented here, does comprise a large number of known and novel biomarker candidates, validates our approach to isolate and characterize the tumour cell secretome in vitro as a rich source for tumour biomarkers.
引用
收藏
页码:47 / 61
页数:15
相关论文
共 77 条
[1]   The human plasma proteome - History, character, and diagnostic prospects [J].
Anderson, NL ;
Anderson, NG .
MOLECULAR & CELLULAR PROTEOMICS, 2002, 1 (11) :845-867
[2]   A novel protease homolog differentially expressed in breast and ovarian cancer [J].
Anisowicz, A ;
Sotiropoulou, G ;
Stenman, G ;
Mok, SC ;
Sager, R .
MOLECULAR MEDICINE, 1996, 2 (05) :624-636
[3]   Cadherins and catenins: Role in signal transduction and tumor progression [J].
Behrens, J .
CANCER AND METASTASIS REVIEWS, 1999, 18 (01) :15-30
[4]   The emerging roles of human tissue kallikreins in cancer [J].
Borgoño, CA ;
Diamandis, EP .
NATURE REVIEWS CANCER, 2004, 4 (11) :876-890
[5]   Cancer incidence and mortality in Europe, 2004 [J].
Boyle, P ;
Ferlay, J .
ANNALS OF ONCOLOGY, 2005, 16 (03) :481-488
[6]   Exosomal-like vesicles are present in human blood plasma [J].
Caby, MP ;
Lankar, D ;
Vincendeau-Scherrer, C ;
Raposo, G ;
Bonnerot, C .
INTERNATIONAL IMMUNOLOGY, 2005, 17 (07) :879-887
[7]   ACTIVATION OF KI-RAS 2 GENE IN HUMAN-COLON AND LUNG CARCINOMAS BY 2 DIFFERENT POINT MUTATIONS [J].
CAPON, DJ ;
SEEBURG, PH ;
MCGRATH, JP ;
HAYFLICK, JS ;
EDMAN, U ;
LEVINSON, AD ;
GOEDDEL, DV .
NATURE, 1983, 304 (5926) :507-513
[8]   Protein profiles associated with survival in lung adenocarcinoma [J].
Chen, GA ;
Gharib, TG ;
Wang, H ;
Huang, CC ;
Kuick, R ;
Thomas, DG ;
Shedden, KA ;
Misek, DE ;
Taylor, JMG ;
Giordano, TJ ;
Kardia, SLR ;
Iannettoni, MD ;
Yee, J ;
Hogg, PJ ;
Orringer, MB ;
Hanash, SM ;
Beer, DG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (23) :13537-13542
[9]   The role of the cell-adhesion molecule E-cadherin as a tumour-suppressor gene [J].
Christofori, G ;
Semb, H .
TRENDS IN BIOCHEMICAL SCIENCES, 1999, 24 (02) :73-76
[10]   Cancer proteomics: many technologies, one goal [J].
Conrads, Thomas P. ;
Hood, Brian L. ;
Petricoin, Emmanuel F., III ;
Liotto, Lance A. ;
Veenstra, Timothy D. .
EXPERT REVIEW OF PROTEOMICS, 2005, 2 (05) :693-703