Shen Min, Hung Rayjean J, Brennan Paul, Malaveille Christian, Donato Francesco, Placidi Donatella, Carta Angela, Hautefeuille Agnes, Boffetta Paolo, Porru Stefano
International Agency for Research on Cancer, Lyon, France.
Cancer Epidemiol Biomarkers Prev. 2003 Nov;12(11 Pt 1):1234-40.
Tobacco smoking and occupational exposures are the main known risk factors for bladder cancer, causing direct and indirect damage to DNA. Repair of DNA damage is under genetic control, and DNA repair genes may play a key role in maintaining genome integrity and preventing cancer development. Polymorphisms in DNA repair genes resulting in variation of DNA repair efficiency may therefore be associated with bladder cancer risk. A hospital-based case-control study was conducted in Brescia, Italy, to assess the relationship between polymorphisms in DNA repair genes XRCC1 (Arg(399)Gln), XRCC3 (Thr(241)Met), and XPD (Lys(751)Gln) and bladder cancer risk. A total of 201 male incident bladder cancer cases and 214 male controls with urological nonneoplastic diseases were recruited and frequency-matched on age, period, and hospital of recruitment. Detailed information was collected using a semistructured questionnaire on demographic, dietary, environmental, and occupational factors. Genotypes were determined by PCR-RFLP analysis. The XRCC3 codon 241 variant genotype exhibited a protective effect against bladder cancer [odds ratio (OR), 0.63; 95% confidence interval (CI), 0.42-0.93], which was prominent among heavy smokers (OR, 0.49; 95% CI, 0.28-0.88) but not among never and light smokers. No overall impact of the XRCC1 codon 399 polymorphism was found (OR, 0.86; 95% CI, 0.59-1.28), but a protective influence of the homozygous variant was suggested among heavy smokers (OR, 0.38; 95% CI, 0.14-1.02). XPD polymorphisms did not show an association with bladder cancer (OR, 0.92; 95% CI, 0.62-1.37). There was no statistical evidence of an interaction between these three genetic polymorphisms and either tobacco smoking or occupational exposure to polycyclic aromatic hydrocarbons and aromatic amines. The XRCC3 codon 241 polymorphism had an overall protective effect against bladder cancer that was most apparent among heavy smokers. Similarly, the XRCC1 codon 399 polymorphism also had a protective effect on bladder cancer among heavy smokers. The XPD polymorphism was not, however, associated with bladder cancer risk.
吸烟和职业暴露是已知的膀胱癌主要危险因素,会对DNA造成直接和间接损伤。DNA损伤的修复受基因控制,DNA修复基因可能在维持基因组完整性和预防癌症发生中起关键作用。因此,DNA修复基因的多态性导致DNA修复效率的变化可能与膀胱癌风险相关。在意大利布雷西亚进行了一项基于医院的病例对照研究,以评估DNA修复基因XRCC1(Arg(399)Gln)、XRCC3(Thr(241)Met)和XPD(Lys(751)Gln)的多态性与膀胱癌风险之间的关系。共招募了201例男性新发膀胱癌病例和214例患有泌尿系统非肿瘤性疾病的男性对照,并根据年龄、时期和招募医院进行频率匹配。使用半结构化问卷收集了有关人口统计学、饮食、环境和职业因素的详细信息。通过PCR-RFLP分析确定基因型。XRCC3密码子241变体基因型对膀胱癌具有保护作用[比值比(OR),0.63;95%置信区间(CI),0.42 - 0.93],在重度吸烟者中尤为显著(OR,0.49;95% CI,0.28 - 0.88),但在从不吸烟和轻度吸烟者中不明显。未发现XRCC1密码子399多态性的总体影响(OR,0.86;95% CI,0.59 - 1.28),但在重度吸烟者中提示纯合变体有保护作用(OR,0.38;95% CI,0.14 - 1.02)。XPD多态性与膀胱癌无关联(OR,0.92;95% CI,0.62 - 1.37)。没有统计学证据表明这三种基因多态性与吸烟或职业性接触多环芳烃和芳香胺之间存在相互作用。XRCC3密码子241多态性对膀胱癌具有总体保护作用,在重度吸烟者中最为明显。同样,XRCC1密码子399多态性在重度吸烟者中对膀胱癌也有保护作用。然而,XPD多态性与膀胱癌风险无关。