Slattery Martha L, Wolff Roger K, Herrick Jennifer S, Caan Bette J, Potter John D
School of Medicine, University of Utah, Salt Lake City, UT 84108, USA.
Cancer Causes Control. 2007 Dec;18(10):1095-105. doi: 10.1007/s10552-007-9049-x. Epub 2007 Aug 13.
Inflammation appears to play a key role in the development of colorectal cancer (CRC). In this study we examine factors involved in the regulation of inflammation and risk of CRC. Data from a multi-center case-control study of colon (N = 1579 cases and N = 1977 controls) and rectal (N = 794 cases and N = 1005 controls) cancer were used to evaluate the association between the rs1800795 and rs1800796 IL6 polymorphisms and CRC. We evaluated the joint effects of IL6 single nucleotide polymorphisms and regular use of aspirin/NSAIDs and vitamin D receptor (VDR) genotype. Having a C allele of the rs1800796 IL6 polymorphisms and the GG genotype of the rs1800795 IL6 polymorphisms was associated with a statistically significantly reduced the risk of colon (OR 0.76 95% CI 0.57, 1.00), but not rectal (OR 1.49 95% CI 1.02,2.16) cancer. Both IL6 polymorphisms were associated with significant interaction with current use of aspirin/NSAIDs to alter risk of colon cancer: individuals with a C allele in either polymorphism who were current users of aspirin/NSAIDs had the lowest colon cancer risk. CRC risk also was associated with an interaction between VDR and IL6 genotypes that was modified by current use of aspirin/NSAIDs. This study provides further support for inflammation-related factors in the etiology of CRC. Other studies are needed to explore other genes in this and other inflammation-related pathways.
炎症似乎在结直肠癌(CRC)的发生发展中起关键作用。在本研究中,我们考察了参与炎症调节及CRC风险的因素。来自一项多中心结肠癌(N = 1579例病例和N = 1977例对照)和直肠癌(N = 794例病例和N = 1005例对照)病例对照研究的数据,用于评估IL6基因多态性rs1800795和rs1800796与CRC之间的关联。我们评估了IL6单核苷酸多态性与阿司匹林/非甾体抗炎药(NSAIDs)的常规使用以及维生素D受体(VDR)基因型的联合效应。携带rs1800796 IL6基因多态性的C等位基因和rs1800795 IL6基因多态性的GG基因型与结肠癌风险在统计学上显著降低相关(比值比[OR] 0.76,95%置信区间[CI] 0.57,1.00),但与直肠癌风险无关(OR 1.49,95% CI 1.02,2.16)。两种IL6基因多态性均与当前使用阿司匹林/NSAIDs改变结肠癌风险存在显著交互作用:任一基因多态性中携带C等位基因且当前使用阿司匹林/NSAIDs的个体患结肠癌风险最低。CRC风险还与VDR和IL6基因型之间的交互作用相关,而这种交互作用会因当前使用阿司匹林/NSAIDs而改变。本研究为CRC病因中与炎症相关的因素提供了进一步支持。还需要其他研究来探索此炎症相关途径及其他途径中的其他基因。