Vogel Ulla, Christensen Jane, Dybdahl Marianne, Friis Søren, Hansen Rikke D, Wallin Håkan, Nexø Bjørn A, Raaschou-Nielsen Ole, Andersen Paal S, Overvad Kim, Tjønneland Anne
National Research Centre for the Working Environment, Copenhagen, Denmark.
Mutat Res. 2007 Nov 1;624(1-2):88-100. doi: 10.1016/j.mrfmmm.2007.04.006. Epub 2007 Apr 27.
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 PPARgamma2 Pro(12)Ala and alcohol was found, where alcohol use was associated with a 22% increased risk of CRC per 10g 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.
炎症性肠病易患结直肠癌,而使用非甾体抗炎药(NSAIDs)可降低风险;因此,改变炎症反应的基因变异可能会改变结直肠癌(CRC)的风险。本研究的目的是确定与炎症反应改变相关的多态性是否与结直肠癌风险相关,并研究其与饮酒、吸烟和使用NSAIDs等生活方式因素之间可能存在的相互作用。我们在“饮食、癌症与健康”前瞻性研究中,对355例腺癌病例和753名对照者进行了研究。这些多态性均与结直肠癌风险无关。发现PPARgamma2 Pro(12)Ala与饮酒之间存在统计学显著的相互作用,即对于携带变异等位基因的个体,每天每摄入10克酒精,患CRC的风险增加22%,而在纯合野生型等位基因携带者中则无此关联(交互作用P值 = 0.02)。此外,还发现DLG5 R30Q与使用NSAIDs之间存在相互作用(交互作用P值 = 0.02)。我们的研究结果表明,炎症反应的先天性变异在结直肠癌风险中未发挥主要作用。