Murine fecal proteomics: A model system for the detection of potential biomarkers for colorectal cancer

被引:36
作者
Ang, Ching-Seng [2 ]
Rothacker, Julie
Patsiouras, Heather
Burgess, Antony W. [2 ]
Nice, Edouard C. [1 ,2 ]
机构
[1] Royal Melbourne Hosp, Prot Biosensing Lab, Ludwig Inst Canc Res, Melbourne Tumour Biol Branch, Melbourne, Vic 3050, Australia
[2] Univ Melbourne, Melbourne, Vic 3010, Australia
基金
英国医学研究理事会;
关键词
Murine fecal proteomics; Apc(Min/+) mice; Colorectal cancer; Biomarkers; Nano-LC-ESI-MS/MS analysis; 2-DIMENSIONAL GEL-ELECTROPHORESIS; MULTIPLE INTESTINAL NEOPLASIA; LYMPH-NODE METASTASIS; FC-GAMMA-BP; OCCULT BLOOD; BINDING-PROTEIN; COLON-CANCER; MOLECULAR-CLONING; SERUM BIOMARKERS; PLASMA PROTEOME;
D O I
10.1016/j.chroma.2009.10.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Tumor related products shed into the feces offer a potential source of biomarkers for the detection of colorectal cancer (CRC). Using SDS-PAGE followed by nanoflow reversed-phased LC-MS/MS to analyse fecal samples from Apc(Min/+) mice (that develop spontaneous multiple intestinal neoplasia with age) we have identified 336 proteins (115 proteins of murine origin, 201 from fecal bacteria, 18 associated with food intake and 2 of apparent parasitic origin). 75% of the murine proteins identified in this study are predicted to be extracellular or associated with the cell plasma membrane. Of these proteins, a number of the murine homologues of colorectal cancer associated proteins (CCAP) such as hemoglobin. haptoglobin, hemopexin, alpha-2-macroglobulin and cadherin-17 have been identified, demonstrating the potential of fecal proteomics for detecting potential biomarkers and paving the way for subsequent MS/MS based biomarker studies on similar human samples. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:3330 / 3340
页数:11
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