Genetic polymorphisms of ADH1B, ADH1C and ALDH2, alcohol consumption, and the risk of gastric cancer: the Japan Public Health Center-based prospective study

被引:59
作者
Hidaka, Akihisa [1 ]
Sasazuki, Shizuka [1 ]
Matsuo, Keitaro [2 ]
Ito, Hidemi [3 ]
Sawada, Norie [1 ]
Shimazu, Taichi [1 ]
Yamaji, Taiki [1 ]
Iwasaki, Motoki [1 ]
Inoue, Manami [1 ,4 ]
Tsugane, Shoichiro [1 ]
机构
[1] Natl Canc Ctr, Res Ctr Canc Prevent & Screening, Epidemiol & Prevent Grp, Tokyo 1040045, Japan
[2] Kyushu Univ, Dept Prevent Med, Fac Med Sci, Fukuoka 8128582, Japan
[3] Aichi Canc Ctr, Res Inst, Div Epidemiol & Prevent, Nagoya, Aichi 4648681, Japan
[4] Univ Tokyo, Grad Sch Med, Tokyo 1130033, Japan
关键词
ALDEHYDE DEHYDROGENASE-2 GENOTYPES; POPULATION-BASED COHORT; STOMACH-CANCER; LINE SURVEY; DRINKING; ACETALDEHYDE; METABOLISM; ESOPHAGEAL; SMOKING; JPHC;
D O I
10.1093/carcin/bgu244
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The association between alcohol consumption, alcohol (ADH), aldehyde dehydrogenase (ALDH) polymorphisms and gastric cancer remains elusive. To find the relation between alcohol consumption and gastric cancer, it is important to consider both alcohol consumption level and ADH1C, ALDH2 polymorphisms.The association between alcohol consumption, genetic polymorphisms of alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH) and gastric cancer risk is not completely understood. We investigated the association between ADH1B (rs1229984), ADH1C (rs698) and ALDH2 (rs671) polymorphisms, alcohol consumption and the risk of gastric cancer among Japanese subjects in a population-based, nested, case-control study (1990-2004). Among 36 745 subjects who answered the baseline questionnaire and provided blood samples, 457 new gastric cancer cases matched to 457 controls were used in the analysis. The odds ratios (OR) and corresponding 95% confidence intervals (CI) were calculated using logistic regression models. No association was observed between alcohol consumption, ADH1B (rs1229984), ADH1C (rs698) and ALDH2 (rs671) polymorphisms and gastric cancer risk. However, considering gene-environmental interaction, ADH1C G allele carriers who drink a parts per thousand yen150g/week of ethanol had a 2.5-fold increased risk of gastric cancer (OR = 2.54, 95% CI = 1.05-6.17) relative to AA genotype carriers who drink 0 to < 150g/week (P for interaction = 0.02). ALDH2 A allele carriers who drink a parts per thousand yen150g/week also had an increased risk (OR = 2.08, 95% CI = 1.05-4.12) relative to GG genotype carriers who drink 0 to < 150g/week (P for interaction = 0.08). To find the relation between alcohol consumption and gastric cancer risk, it is important to consider both alcohol consumption level and ADH1C and ALDH2 polymorphisms.
引用
收藏
页码:223 / 231
页数:9
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