Wang Yuan-Hung, Yeh Shauh-Der, Shen Kun-Hung, Shen Cheng-Huang, Juang Guang-Dar, Hsu Ling-I, Chiou Hung-Yi, Chen Chien-Jen
School of Public Health, Taipei Medical University, Taipei 110, Taiwan.
Toxicol Appl Pharmacol. 2009 Nov 15;241(1):111-8. doi: 10.1016/j.taap.2009.08.008. Epub 2009 Aug 15.
Cigarette smoking, arsenic and occupational exposures are well-known risk factors for the development of urothelial carcinoma (UC). Therefore, the aim of this study is to investigate whether the effect of cigarette smoking, alcohol consumption, arsenic and occupational exposures on risk of UC could be modified by genetic polymorphisms of cytochrome P450 2E1 and glutathione S-transferase omega. A hospital-based case-control study consisted of 520 histologically confirmed UC cases, and 520 age- and gender-matched cancer-free controls were carried out from September 1998 to December 2007. Genotyping of CYP2E1, GSTO1 and GSTO2 was determined by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Subjects with both of cigarette smoking and alcohol consumption have a significantly increased UC risk (odds ratio [OR]=2.9; 95% confidence interval [CI]=1.9-4.4). Significantly increased UC risks of 1.5 and 1.9 were found for study subjects with high arsenic exposure and those who have been exposed to two or more occupational exposures, respectively. A significantly increased UC risk of 3.9 was observed in study subjects with H2-H2 diplotype of GSTO1 and GSTO2. The significantly highest UC risk of 9.0 was found for those with all environmental risk factors of cigarette smoking, alcohol consumption, arsenic and occupational exposures and two or more risk genotypes/diplotypes of CYP2E1, GSTO1 and GSTO2. Our findings suggest that a significantly joint effect of cigarette smoking, alcohol consumption, arsenic and occupational exposures and risk genotypes/diplotypes of CYP2E1, GSTO1 and GSTO2 on risk of UC was found.
吸烟、接触砷和职业暴露是已知的尿路上皮癌(UC)发生的危险因素。因此,本研究的目的是调查吸烟、饮酒、接触砷和职业暴露对UC风险的影响是否会因细胞色素P450 2E1和谷胱甘肽S-转移酶ω的基因多态性而改变。一项基于医院的病例对照研究包括520例经组织学确诊的UC病例,并于1998年9月至2007年12月选取了520名年龄和性别匹配的无癌对照。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)确定CYP2E1、GSTO1和GSTO2的基因分型。同时有吸烟和饮酒的受试者患UC的风险显著增加(优势比[OR]=2.9;95%置信区间[CI]=1.9-4.4)。高砷暴露的研究对象和接触两种或更多职业暴露的研究对象患UC的风险分别显著增加1.5倍和1.9倍。GSTO1和GSTO2的H2-H2双倍型的研究对象患UC的风险显著增加3.9倍。对于具有吸烟、饮酒、接触砷和职业暴露等所有环境危险因素以及两种或更多CYP2E1、GSTO1和GSTO2风险基因型/双倍型的人群,发现患UC的风险最高,达9.0倍。我们的研究结果表明,吸烟、饮酒、接触砷和职业暴露与CYP2E1、GSTO1和GSTO2的风险基因型/双倍型对UC风险存在显著的联合作用。