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首页> 外文期刊>Cancer causes and control: CCC >Influence of NQO1, ALDH2, and CYP2E1 genetic polymorphisms, smoking, and alcohol drinking on the risk of lung cancer in Koreans.
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Influence of NQO1, ALDH2, and CYP2E1 genetic polymorphisms, smoking, and alcohol drinking on the risk of lung cancer in Koreans.

机译:NQO1,ALDH2和CYP2E1基因多态性,吸烟和饮酒对韩国人肺癌风险的影响。

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OBJECTIVES: We investigated the association of genetic polymorphisms of NQO1, ALDH2, CYP2E1, and the combined genotype of these genes on lung cancer risk, and also evaluated the association after stratification by cumulative smoking amounts and alcohol drinking levels. METHODS: The case-control study was performed in 387 lung cancer patients and 387 age- and sex-matched cancer-free controls. Direct interview was conducted and the genotypes of NQO1, ALDH2, and CYP2E1 were investigated using PCR-RFLP or 5'-nuclease activity assay. RESULTS: The proportion of individuals with occupational history of mining was significantly higher in cases than in controls. The risk of lung cancer was significantly lower in light-drinkers (<108 g/week) than non-drinkers. The NQO1 Pro/Ser + Ser/Ser genotype showed an increased risk for lung cancer with a marginal significance (OR = 1.35, 95% CI = 0.99-1.86) compared with NQO1 Pro/Pro genotype. In heavy-smokers, the combination of NQO1 Pro/Ser + Ser/Ser and CYP2E1 c1/c1 genotype was associated with a significantly increased risk for lung cancer (OR = 2.25, 95% CI = 1.14-4.43) compared with those of NQO1 Pro/Pro and CYP2E1 c1/c2 + c2/c2 genotype. We found a significant interaction between alcohol drinking level and the CYP2E1 genotype (P = 0.0227). CONCLUSIONS: Our result suggests that the risk of lung cancer is affected by smoking, alcohol drinking, and the genetic polymorphism of NQO1. In particular, genetic polymorphisms for NQO1, CYP2E1, and ALDH2 synergistically with cumulative smoking amounts and alcohol drinking levels interact in the carcinogenesis of lung cancer in Koreans.
机译:目的:我们调查了NQO1,ALDH2,CYP2E1的遗传多态性与这些基因的联合基因型与肺癌风险的关联,并通过分层吸烟量和饮酒水平对分层后的关联进行了评估。方法:对387名肺癌患者以及387名年龄和性别匹配的无癌对照组进行了病例对照研究。进行了直接访谈,并使用PCR-RFLP或5'-核酸酶活性分析研究了NQO1,ALDH2和CYP2E1的基因型。结果:具有采矿业职业病史的个体比例明显高于对照组。轻饮者(<108 g /周)患肺癌的风险显着低于非饮酒者。与NQO1 Pro / Pro基因型相比,NQO1 Pro / Ser + Ser / Ser基因型显示出患肺癌的风险增加,具有边际意义(OR = 1.35,95%CI = 0.99-1.86)。在重度吸烟者中,与NQO1相比,NQO1 Pro / Ser + Ser / Ser和CYP2E1 c1 / c1基因型的组合与肺癌风险显着增加(OR = 2.25,95%CI = 1.14-4.43) Pro / Pro和CYP2E1 c1 / c2 + c2 / c2基因型。我们发现饮酒水平与CYP2E1基因型之间存在显着的相互作用(P = 0.0227)。结论:我们的结果表明吸烟,饮酒和NQO1基因多态性会影响肺癌的风险。特别是,NQO1,CYP2E1和ALDH2的遗传多态性与累积吸烟量和饮酒水平协同作用在韩国人肺癌的致癌作用中相互作用。

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