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Human bladder cancer risk calculation based on genome-wide analysis of genetic variants.

机译:基于基因组遗传变异分析的人膀胱癌风险计算。

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摘要

Urinary bladder cancer is the ninth most common cancer worldwide (Roth et al. 2012; Golka et al. 2011). The strongest known risk factors are cigarette smoking, occupational exposure to bladder carcinogens and male gender (Golka et al. 2012a, b; Ovsiannikov et al. 2012). It is well established that slow acetylation (NAT2) and a deletion variant of glutathione S-transferase Ml (GSTM1) are associated with increased bladder cancer risk (Schwender et al. 2012; Bell et al. 1993; Cartwright et al. 1984; Golka et al. 1996; Kempkes et al. 1996; Hengstler et al. 1998).
机译:膀胱癌是全世界第九次常见的癌症(Roth等,2012; Golka等人2011)。 最强烈的已知风险因素是吸烟,患有膀胱癌和男性性别的职业暴露(Golka等,2012A,B; Ovsiannikov等,2012)。 很好地确定,慢乙酰化(NAT2)和谷胱甘肽S-转移酶m1(GSTM1)的缺失变体与增加的膀胱癌风险有关(Schwender等,2012; Bell等人1993; Cartwright等1984; Golka 等人。1996; kempkes等。1996;恒星等人1998)。

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