Aldehyde dehydrogenase 2 (ALDH2) and alcohol dehydrogenase 1B (ADH1B) polymorphisms exacerbate bladder cancer risk associated with alcohol drinking: gene-environment interaction

被引:30
|
作者
Masaoka, Hiroyuki [1 ,2 ]
Ito, Hidemi [3 ,4 ]
Soga, Norihito [5 ]
Hosono, Satoyo [3 ]
Oze, Isao [3 ]
Watanabe, Miki [3 ]
Tanaka, Hideo [3 ,4 ]
Yokomizo, Akira [2 ]
Hayashi, Norio [5 ]
Eto, Masatoshi [2 ]
Matsuo, Keitaro [1 ,4 ]
机构
[1] Aichi Canc Ctr, Div Mol Med, Res Inst, Nagoya, Aichi 4648681, Japan
[2] Kyushu Univ, Grad Sch Med Sci, Dept Urol, Fukuoka 8128582, Japan
[3] Aichi Canc Ctr, Div Epidemiol & Prevent, Res Inst, Nagoya, Aichi 4648681, Japan
[4] Nagoya Univ, Dept Epidemiol, Grad Sch Med, Nagoya, Aichi 4660065, Japan
[5] Aichi Canc Ctr Hosp, Dept Urol, Nagoya, Aichi 4648681, Japan
关键词
ESOPHAGEAL CANCER; NECK-CANCER; ACETALDEHYDE CONCENTRATIONS; ETHANOL INGESTION; DNA-ADDUCTS; METAANALYSIS; CONSUMPTION; POPULATION; SMOKING; BLOOD;
D O I
10.1093/carcin/bgw033
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Those with ALDH2 Glu/Lys genotype and the ADH1B Arg allele were associated with an increased risk of bladder cancer (BCa). Gene-environment interaction between ALDH2 Glu/Lys and alcohol drinking might indicate that acetaldehyde contributes to a development of BCa.Although a range of chemical exposures (cigarette smoking and occupational exposure) are recognized risk factors for the development of bladder cancer (BCa), many epidemiological studies have demonstrated that alcohol drinking is not associated with BCa risk. Aldehyde dehydrogenase 2 (ALDH2; rs671, Glu504Lys) and alcohol dehydrogenase 1B (ADH1B; rs1229984, His47Arg) polymorphisms impact the accumulation of acetaldehyde, resulting in an increased risk of various cancers. To date, however, no studies evaluating the association between BCa risk and alcohol drinking have considered these polymorphisms. Here, we conducted a matched case-control study to investigate whether ALDH2 and ADH1B polymorphisms influence BCa risk associated with alcohol drinking. Cases were 74 BCa patients and controls were 740 first-visit outpatients without cancer at Aichi Cancer Center Hospital between January 2001 and December 2005. Odds ratio (OR), 95% confidence interval (CI) and gene-environment interaction were assessed by conditional logistic regression analysis with adjustment for potential confounders. Results showed that ALDH2 Glu/Lys was associated with a significantly increased risk of BCa compared with Glu/Glu (OR 2.03, 95% CI 1.14-3.62, P = 0.017). In contrast, ALDH2 Glu/Lys showed no increase in risk among the stratum of never drinkers compared with Glu/Glu, indicating a gene-environment interaction. ADH1B His/Arg had an OR of 1.98 (1.20-3.24, P = 0.007) compared with His/His. ADH1B Arg+ showed a similar OR and 95% CI. Individuals with ALDH2 Glu/Lys and ADH1B Arg+ had the highest risk of BCa compared with ALDH2 Glu/Glu and ADH1B His/His [OR 4.00 (1.81-8.87), P = 0.001].
引用
收藏
页码:583 / 588
页数:6
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