Dietary, lifestyle and clinicopathological factors associated with APC mutations and promoter methylation in colorectal cancers from the EPIC-Norfolk study

被引:52
作者
Gay, Laura J. [1 ]
Mitrou, Panagiota N. [2 ]
Keen, Jennifer [1 ]
Bowman, Richard [1 ]
Naguib, Adam [1 ]
Cooke, James [1 ]
Kuhnle, Gunter G. [1 ,2 ,3 ]
Burns, Philip A. [4 ]
Luben, Robert [5 ]
Lentjes, Marleen [2 ]
Khaw, Kay-Tee [5 ]
Ball, Richard Y. [6 ]
Ibrahim, Ashraf E. K. [7 ]
Arends, Mark J. [7 ]
机构
[1] MRC, Dunn Human Nutr Unit, Cambridge, England
[2] Univ Cambridge, Ctr Nutr Epidemiol Canc Prevent & Survival, MRC, Cambridge CB2 0QQ, England
[3] Univ Reading, Dept Food & Nutr Sci, Reading RG6 2AH, Berks, England
[4] St James Univ Hosp, Leeds Inst Mol Med, Leeds, W Yorkshire, England
[5] Univ Cambridge, Dept Publ Hlth & Primary Care, Cambridge CB2 0QQ, England
[6] Norfolk & Norwich Univ Hosp, Norfolk & Waveney Cellular Pathol Network, Norwich, Norfolk, England
[7] Univ Cambridge, Dept Pathol, Cambridge CB2 0QQ, England
基金
英国医学研究理事会;
关键词
colorectal; cancer; APC; mutation; diet; clinicopathological; promoter; methylation; N-nitroso; compounds; FAMILIAL ADENOMATOUS POLYPOSIS; K-RAS MUTATIONS; SOMATIC MUTATIONS; COLON-CANCER; MICROSATELLITE INSTABILITY; NETHERLANDS COHORT; FOLATE-DEFICIENCY; NITROSO-COMPOUNDS; TUMOR-SUPPRESSOR; SPORADIC COLON;
D O I
10.1002/path.4085
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The tumour suppressor APC is the most commonly altered gene in colorectal cancer (CRC). Genetic and epigenetic alterations of APC may therefore be associated with dietary and lifestyle risk factors for CRC. Analysis of APC mutations in the extended mutation cluster region (codons 1276-1556) and APC promoter 1A methylation was performed on 185 archival CRC samples collected from participants of the European Prospective Investigation into Cancer (EPIC)-Norfolk study, with the aim of relating these to high-quality seven-day dietary and lifestyle data collected prospectively. Truncating APC mutations (APC+) and promoter 1A methylation (PM+) were identified in 43% and 23% of CRCs analysed, respectively. Distal CRCs were more likely than proximal CRCs to be APC+ or PM+ (p = 0.04). APC+ CRCs were more likely to be moderately/well differentiated and microsatellite stable than APC- CRCs (p = 0.05 and 0.03). APC+ CRC cases consumed more alcohol than their counterparts (p = 0.01) and PM+ CRC cases consumed lower levels of folate and fibre (p = 0.01 and 0.004). APC+ or PM+ CRC cases consumed higher levels of processed meat and iron from red meat and red meat products (p = 0.007 and 0.006). Specifically, CRC cases harbouring GC-to-AT transition mutations consumed higher levels of processed meat (35 versus 24 g/day, p = 0.04) and iron from red meat and red meat products (0.8 versus 0.6 mg/day, p = 0.05). In a logistic regression model adjusted for age, sex and cigarette-smoking status, each 19 g/day (1SD) increment increase in processed meat consumption was associated with cases with GC-to-AT mutations (OR 1.68, 95% CI 1.032.75). In conclusion, APC+ and PM+ CRCs may be influenced by diet and GC-to-AT mutations in APC are associated with processed meat consumption, suggesting a mechanistic link with dietary alkylating agents, such as N-nitroso compounds. Copyright (c) 2012 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:405 / 415
页数:11
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