Prospective study of interaction between alcohol, NSAID use and polymorphisms in genes involved in the inflammatory response in relation to risk of colorectal cancer

被引:67
作者
Vogel, Ulla [1 ]
Christensen, Jane
Dybdahl, Marianne
Friis, Soren
Hansen, Rikke D.
Wallin, Hakan
Nexo, Bjorn A.
Raaschou-Nielsen, Ole
Andersen, Paal S.
Overvad, Kim
Tjonneland, Anne
机构
[1] Natl Res Ctr Working Environm, Copenhagen, Denmark
[2] Roskilde Univ, Inst Sci Syst & Models, Roskilde, Denmark
[3] Danish Canc Soc, Inst Canc Epidemiol, Copenhagen, Denmark
[4] Statens Serum Inst, Dept Clin Biochem, DK-2300 Copenhagen, Denmark
[5] Univ Aarhus, Inst Human Genet, Aarhus, Denmark
[6] Aarhus Univ Hosp, Aalborg Hosp, Dept Clin Epidemiol, DK-8000 Aarhus, Denmark
关键词
genetic epidemiology; colorectal cancer; prospective study; gene environment interaction; inflammation; PPAR gamma; polymorphism; IL-6; IL8; IL10; NOD2; IL1; beta;
D O I
10.1016/j.mrfmmm.2007.04.006
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Inflammatory bowl disease predisposes to cancer of the colorectum, and the use of non-steroidal anti-inflammatory drugs (NSAIDs) decreases the risk; hence genetic variations that modify the inflammatory response may alter the risk of colorectal cancer (CRC). The purpose of this study was to determine if polymorphisms associated with an altered inflammatory response are associated with colorectal cancer risk, and to investigate the possible interaction with lifestyle factors such as alcohol use, smoking and NSAID) use. We studied 355 adenocarcinoma cases and 753 control persons, nested within the prospective "Diet, Cancer and Health" study. None of the polymorphisms were associated with risk of colorectal cancer. A statistically significant interaction between PPAR gamma 2 Pro(12) Ala and alcohol was found, where alcohol use was associated with a 22% increased risk of CRC per 10 g alcohol/day among carriers of the variant allele but not among homozygous wild type allele carriers (P for interaction = 0.02). Moreover, an interaction between DLG5 R30Q and NSAID use was found (P for interaction = 0.02). Our results do not suggest that inborn variations in the inflammatory response play any major role in risk of colorectal cancer. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:88 / 100
页数:13
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