Alcohol and aldehyde dehydrogenase gene polymorphisms and oropharyngolaryngeal, esophageal and stomach cancers in Japanese alcoholics

被引:213
作者
Yokoyama, A
Muramatsu, T
Omori, T
Yokoyama, T
Matsushita, S
Higuchi, S
Maruyama, K
Ishii, H
机构
[1] Kurihama Natl Hosp, Natl Inst Alcoholism, Yokosuka, Kanagawa 2390841, Japan
[2] Kawasaki Municipal Hosp, Dept Surg, Kawasaki, Kanagawa 2100013, Japan
[3] Keio Univ, Sch Med, Dept Neuropsychiat, Shinjuku Ku, Tokyo 1600016, Japan
[4] Keio Univ, Sch Med, Dept Internal Med, Shinjuku Ku, Tokyo 1600016, Japan
[5] Tokyo Med & Dent Univ, Dept Epidemiol, Inst Med Res, Chiyoda Ku, Tokyo 1010062, Japan
关键词
D O I
10.1093/carcin/22.3.433
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Alcohol dehydrogenase-2 (ADH2) and aldehyde dehydrogenase-2 (ALDH2) gene polymorphisms play roles in ethanol metabolism, drinking behavior and esophageal carcinogenesis in Japanese; however, the combined influence of ADH2 and ALDH2 genotypes on other aerodigestive tract cancers have not been investigated. ADH2/ALDH2 genotyping was performed on lymphocyte DNA samples from Japanese alcoholic men (526 cancer-free; 159 with solitary or multiple aerodigestive tract cancers, including 33 oropharyngolaryngeal, 112 esophageal, 38 stomach and 22 multiple primary cancers in two or three organs). After adjustment for age, drinking and smoking habits, and ADH2/ALDH2 genotypes, the presence of either ADH2*1/2*1 or ALDH2*1/2*2 significantly increased the risk for oropharyngolaryngeal cancer [odds ratios (ORs), 6.68 with;ADH2*1/2*1 and 18.52 with ALDH2*1/2"2] and esophageal cancer (ORs, 2.64 and 13.50, respectively). For patients with both ADH2*1/2*1 and ALDH2*1/2*2, the risks for oropharyngolaryngeal and esophageal cancers were enhanced in a multiplicative fashion (OR = 121.77 and 40,40, respectively). A positive association with ALDH2*1/2*2 alone was observed for stomach cancer patients who also had oropharyngolaryngeal and/or esophageal cancer (OR = 110.58), but it was not observed for those with stomach cancer alone. Furthermore, in the presence of ALDH2*1/2"2, the risks for multiple intra-esophageal cancers (OR = 3.43) and for esophageal cancer with oropharyngolaryngeal and/or stomach cancer (OR = 3.95) were higher than the risks for solitary intra-esophageal cancer and for esophageal cancer alone, but these tendencies were not observed for ADH2*1/2*1 genotype, Alcoholics' population attributable risks due to ADH2/ALDH2 polymorphisms were estimated to be 82.0 % for oropharyngolaryngeal cancer and 63.9% for esophageal cancer.
引用
收藏
页码:433 / 439
页数:7
相关论文
共 51 条
[1]  
*AM PSYCHIAT ASS, 1987, DIAGN STAT MAN MENT, P137
[2]  
[Anonymous], 1985, IARC Monogr Eval Carcinog Risk Chem Hum, V36, P101
[3]  
[Anonymous], 1999, IARC Monogr Eval Carcinog Risks Hum, V71 Pt 2, P319
[4]   ESTIMATING THE POPULATION ATTRIBUTABLE RISK FOR MULTIPLE RISK-FACTORS USING CASE-CONTROL DATA [J].
BRUZZI, P ;
GREEN, SB ;
BYAR, DP ;
BRINTON, LA ;
SCHAIRER, C .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1985, 122 (05) :904-913
[5]   Self-reported flushing and genotypes of ALDH2, ADH2, and ADH3 among Taiwanese Han [J].
Chen, WJ ;
Chen, CC ;
Yu, JM ;
Cheng, ATA .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1998, 22 (05) :1048-1052
[6]   Expression and activities of class IV alcohol dehydrogenase and class III aldehyde dehydrogenase in human mouth [J].
Dong, YJ ;
Peng, TK ;
Yin, SJ .
ALCOHOL, 1996, 13 (03) :257-262
[7]   ACETALDEHYDE METABOLISM IN DIFFERENT ALDEHYDE DEHYDROGENASE-2 GENOTYPES [J].
ENOMOTO, N ;
TAKASE, S ;
YASUHARA, M ;
TAKADA, A .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1991, 15 (01) :141-144
[8]   Detection of DNA adducts of acetaldehyde in peripheral white blood cells of alcohol abusers [J].
Fang, JL ;
Vaca, CE .
CARCINOGENESIS, 1997, 18 (04) :627-632
[9]  
GOEDDE HW, 1992, HUM GENET, V88, P344
[10]  
HARADA S, 1993, ALCOHOL ALCOHOLISM, V28, P11