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Hypopharyngeal cancer risk in Japanese: Genetic polymorphisms related to the metabolism of alcohol- and tobacco-associated carcinogens

机译:日语中的下咽喉癌风险:与烟酒相关致癌物代谢相关的遗传多态性

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Background: Several studies have investigated hypopharyngeal cancer (HC) risk in combination with xenobiotic metabolism-related genetic polymorphisms and the burden of alcohol consumption and smoking in European countries but not in East Asian countries. Patients and Methods: This hospital-based case–control study involved 61 male patients with HC and 71 male cancer-free controls. Information on age, body mass index, and alcohol and cigarette consumption was obtained from medical records, a self-completion questionnaire, and a thorough interview by an otolaryngologist. Alcohol dehydrogenase 1B (ADH1B), aldehyde dehydrogenase 2 (ALDH2), cytochrome P450 A1 (CYP1A1) MspI, CYP1A1 Ile462Val, glutathione S-transferase (GST) M1, GSTT1, and GSTP1 gene polymorphisms were determined by polymerase chain reaction-based methods. Univariate and multivariate analyses were performed by adjustment for age by the Mantel–Haenszel method. Results: The burden of alcohol and cigarette consumption significantly increased the risk of HC and showed a synergistic effect. ADH1B*1/*1 (odds ratio [OR] 7.34) and ALDH2 *1/*2 (OR 13.22) were significant risk factors for HC. Individuals with ADH1B*1/*1 or ALDH2 *1/*2 who consumed alcohol were more susceptible to HC. However, polymorphisms of CYP1A1 gene and GSTs were not significant cancer risk factors in patients with HC. Conclusions: ADH1B*1/*1 and ALDH2 *1/*2 were significant risk factors for HC, while polymorphism of CYP1A1 gene and GSTs was not a significant risk factor for HC. These polymorphisms determined the effects of alcohol and cigarette smoke in addition to burden of alcohol and cigarettes intake on the risk of HC.
机译:背景:在欧洲国家(而非东亚国家),有几项研究调查了下咽癌(HC)与异种代谢相关遗传多态性以及饮酒和吸烟负担的风险。患者和方法:这项基于医院的病例对照研究涉及61例男性HC患者和71例男性无癌对照。有关年龄,体重指数以及饮酒和吸烟的信息是从医疗记录,自我完成调查表以及耳鼻喉科医生的全面访谈中获得的。通过聚合酶链反应法确定了乙醇脱氢酶1B(ADH1B),醛脱氢酶2(ALDH2),细胞色素P450 A1(CYP1A1)MspI,CYP1A1 Ile462Val,谷胱甘肽S-转移酶(GST)M1,GSTT1和GSTP1基因多态性。单变量和多变量分析通过Mantel–Haenszel方法校正年龄。结果:饮酒和吸烟的负担显着增加了患HC的风险,并显示出协同作用。 ADH1B * 1 / * 1(比值比[OR] 7.34)和ALDH2 * 1 / * 2(OR 13.22)是HC的重要危险因素。饮酒的患有ADH1B * 1 / * 1或ALDH2 * 1 / * 2的人更容易感染HC。然而,CYP1A1基因和GSTs的多态性并不是HC患者的重要癌症危险因素。结论:ADH1B * 1 / * 1和ALDH2 * 1 / * 2是HC的重要危险因素,而CYP1A1基因和GSTs的多态性不是HC的重要危险因素。这些多态性决定了酒精和香烟烟雾以及酒精和香烟摄入量对HC风险的影响。

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