Proteomic profiling of a mouse model of acute intestinal Apc deletion leads to identification of potential novel biomarkers of human colorectal cancer (CRC)

被引:31
作者
Hammoudi, Abeer [1 ]
Song, Fei [1 ]
Reed, Karen R. [2 ]
Jenkins, Rosalind E. [3 ]
Meniel, Valerie S. [2 ]
Watson, Alastair J. M. [4 ]
Pritchard, D. Mark [1 ]
Clarke, Alan R. [2 ]
Jenkins, John R. [1 ]
机构
[1] Univ Liverpool, Inst Translat Med, Dept Gastroenterol, Liverpool L69 3GE, Merseyside, England
[2] Cardiff Univ, European Canc Stem Cell Res Inst, Cardiff CF24 4HQ, S Glam, Wales
[3] Univ Liverpool, Inst Translat Med, MRC, Ctr Drug Safety Sci, Liverpool L69 3BX, Merseyside, England
[4] Univ E Anglia, Norwich Med Sch, Norwich NR4 7TJ, Norfolk, England
关键词
Adenomatous polyposis coli; Biomarkers; Colorectal cancer; Proteomics; DISCOVERY; CARCINOMA; CELLS;
D O I
10.1016/j.bbrc.2013.08.076
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Colorectal cancer (CRC) is the fourth most common cause of cancer-related death worldwide. Accurate non-invasive screening for CRC would greatly enhance a population's health. Adenomatous polyposis coli (Apc) gene mutations commonly occur in human colorectal adenomas and carcinomas, leading to Wnt signalling pathway activation. Acute conditional transgenic deletion of Apc in murine intestinal epithelium (AhCre(+)/Apc(fl/fl)) causes phenotypic changes similar to those found during colorectal tumouri-genesis. This study comprised a proteomic analysis of murine small intestinal epithelial cells following acute Apc deletion to identify proteins that show altered expression during human colorectal carcinogenesis, thus identifying proteins that may prove clinically useful as blood/serum biomarkers of colorectal neoplasia. Eighty-one proteins showed significantly increased expression following iTRAQ analysis, and validation of nine of these by Ingenuity Pathaway Analysis showed they could be detected in blood or serum. Expression was assessed in AhCre(+)Apc(fl/fl) small intestinal epithelium by immunohistochemistry, western blot and quantitative real-time PCR; increased nucelolin concentrations were also detected in the serum of AhCre(+)Apc(fl/fl) and Apc(Mm/+) mice by ELISA. Six proteins; heat shock 60 kDa protein 1, Nucleolin, Prohibitin, Cytokeratin 18, Ribosomal protein L6 and DEAD (Asp-Glu-Ala-Asp) box polypeptide 5,were selected for further investigation. Increased expression of 4 of these was confirmed in human CRC by qPCR. In conclusion, several novel candidate biomarkers have been identified from analysis of transgenic mice in which the Apc gene was deleted in the intestinal epithelium that also showed increased expression in human CRC. Some of these warrant further investigation as potential serum-based biomarkers of human CRC. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:364 / 370
页数:7
相关论文
共 24 条
[1]   The topoisomerase II-Hsp90 complex: A new chemotherapeutic target? [J].
Barker, CR ;
Hamlett, J ;
Pennington, SR ;
Burrows, F ;
Lundgren, K ;
Lough, R ;
Watson, AJM ;
Jenkins, JR .
INTERNATIONAL JOURNAL OF CANCER, 2006, 118 (11) :2685-2693
[2]   Diagnostic accuracy of faecal occult blood tests used in screening for colorectal cancer: a systematic review [J].
Burch, J. A. ;
Soares-Weiser, K. ;
St John, D. J. B. ;
Duffy, S. ;
Smith, S. ;
Kleijnen, J. ;
Westwood, M. .
JOURNAL OF MEDICAL SCREENING, 2007, 14 (03) :132-137
[3]   Wnt signalling in adenomas of familial adenomatous polyposis patients [J].
Caldwell, G. M. ;
Jones, C. E. ;
Ashley, A. M. ;
Wei, W. ;
Hejmadi, R. K. ;
Morton, D. G. ;
Matthews, G. M. .
BRITISH JOURNAL OF CANCER, 2010, 103 (06) :910-917
[4]   The genetics of colorectal cancer [J].
Calvert, PM ;
Frucht, H .
ANNALS OF INTERNAL MEDICINE, 2002, 137 (07) :603-612
[5]   Identification of prohibitin as a potential biomarker for colorectal carcinoma based on proteomics technology [J].
Chen, Debo ;
Chen, Fenglin ;
Lu, Xingrong ;
Yang, Xiaosong ;
Xu, Zhongbin ;
Pan, Jie ;
Huang, Ying ;
Lin, Huiming ;
Chi, Pan .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2010, 37 (02) :355-365
[6]   The ABC of APC [J].
Fearnhead, NS ;
Britton, MP ;
Bodmer, WF .
HUMAN MOLECULAR GENETICS, 2001, 10 (07) :721-733
[7]   Mining the plasma proteome for cancer biomarkers [J].
Hanash, Samir M. ;
Pitteri, Sharon J. ;
Faca, Vitor M. .
NATURE, 2008, 452 (7187) :571-579
[8]   Cochrane systematic review of colorectal cancer screening using the fecal occult blood test (Hemoccult): An update [J].
Hewitson, Paul ;
Glasziou, Paul ;
Watson, Eila ;
Towler, Bernie ;
Irwig, Les .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2008, 103 (06) :1541-1549
[9]   A proteomic approach to identifying new drug targets (potentiating topoisomerase II poisons) [J].
Jenkins, J. R. .
BRITISH JOURNAL OF RADIOLOGY, 2008, 81 :S69-S77
[10]   Clinical Validation of Colorectal Cancer Biomarkers Identified from Bioinformatics Analysis of Public Expression Data [J].
Jung, Yeonjoo ;
Lee, Sanghyuk ;
Choi, Hyung-Seok ;
Kim, Soon-Nam ;
Lee, Eunyoung ;
Shin, Youngah ;
Seo, Jihae ;
Kim, Bumjin ;
Jung, Yeonhwa ;
Kim, Wan Kyu ;
Chun, Ho-Kyung ;
Lee, Woo Yong ;
Kim, Jaesang .
CLINICAL CANCER RESEARCH, 2011, 17 (04) :700-709