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XRCC1基因多态性、饮酒与结直肠癌风险:中国江苏省的一项病例对照研究

Polymorphisms in XRCC1 gene, alcohol drinking, and risk of colorectal cancer: a case-control study in Jiangsu Province of China.

作者信息

Gao Chang-Ming, Ding Jian-Hua, Li Su-Ping, Liu Yan-Ting, Cao Hai-Xia, Wu Jian-Zhong, Tang Jin-Hai, Tajima Kazuo

机构信息

Division of Epidemiology, Jiangsu Province Institute of Cancer Research, Nanjing, Jiangsu Province, China E-mail :

出版信息

Asian Pac J Cancer Prev. 2014 Jan;14(11):6613-8. doi: 10.7314/apjcp.2013.14.11.6613.

Abstract

To evaluate the relationship between alcohol drinking, XRCC1 codon 194 and 399 polymorphisms and risk of colorectal cancer, we conducted a case-control study with 315 colorectal cancer cases (105 colon, 210 rectal) and 439 population-based controls in Jiangsu Province of China. The XRCC1 codon 194 and 399 genotypes were identified using polymerase chain reaction and restrictrion fragment length polymorphism methods (PCR-RFLP). A structured questionnaire was used to elicit detailed information. Odds ratios (ORs) were estimated with an unconditional logistic model. In this study no significant differences were observed among the studied groups with regard to the genotype distribution of the XRCC1 codons 194 and 399 and the risk of colorectal cancer did not appear to be significantly influenced by genotype alone, whereas alcohol consumption showed a positive association (P for trend <0.01). When combined effects of XRCC1 polymorphisms and alcohol consumption were analyzed, we found that the 194Trp or 399Gln alleles further increased the colorectal cancer risk due to high alcohol intake. These findings support the conclusion that colorectal cancer susceptibility may be altered by gene-environment interactions.

摘要

为了评估饮酒、XRCC1基因194和399密码子多态性与结直肠癌风险之间的关系,我们在中国江苏省开展了一项病例对照研究,研究对象包括315例结直肠癌患者(105例结肠癌、210例直肠癌)和439名基于人群的对照。采用聚合酶链反应和限制性片段长度多态性方法(PCR-RFLP)鉴定XRCC1基因194和399密码子的基因型。使用结构化问卷获取详细信息。采用非条件逻辑模型估计比值比(OR)。在本研究中,研究组之间在XRCC1基因194和399密码子的基因型分布方面未观察到显著差异,结直肠癌风险似乎不受基因型单独显著影响,而饮酒显示出正相关(趋势P<0.01)。当分析XRCC1多态性与饮酒的联合效应时,我们发现194Trp或399Gln等位基因因高酒精摄入量进一步增加了结直肠癌风险。这些发现支持以下结论:结直肠癌易感性可能因基因-环境相互作用而改变。

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