Genetic polymorphisms in cytochrome P4502E1, alcohol and aldehyde dehydrogenases and the risk of esophageal squamous cell carcinoma in Gansu Chinese males | |
Guo, YM; Wang, Q; Liu, YZ; Chen, HM; Qi, Z; Guo, QH; Guo, YM (reprint author), Gansu Coll Tradit Chinese Med, Dept Clin Med, Lanzhou 730000, Gansu, Peoples R China. | |
刊名 | WORLD JOURNAL OF GASTROENTEROLOGY |
2008-03-07 | |
卷号 | 14期号:9页码:1444-1449 |
关键词 | esophageal squamous cell carcinoma cytochromes P4502E1 alcohol dehydrogenases aldehyde dehydrogenases genetic polymorphisms |
ISSN号 | 1007-9327 |
DOI | 10.3748/wjg.14.1444 |
文献子类 | Article |
英文摘要 | AIM: To evaluate the association between genetic polymorphisms in CYP2E1, ALDH2 and ADH1B and the risk of esophageal squamous cell carcinoma (ESCC) in a high risk area of Gansu province, in Chinese males. METHODS: A case-control study was conducted to investigate the genetic polymorphisms of these enzymes (CYP2E1*c1/*c2, ALDH2*1/*2 and ADH1B *1/*1 genotypes). A total of 80 esophageal cancer cases and 480 controls were recruited. RESULTS: Compared with controls, cases had a greater prevalence of heavier alcohol consumption (53.8% vs 16.2%) and a higher proportion of alcohol drinkers with > 30 drink-years (28.8% vs 13.5%). Heavier alcohol consumption and alcohol drinking with > 30 drink-years increased the risk of ESCC, with ORs (95% CI) of 3.20 (1.32-9.65) and 1.68 (0.96-3.21). CYP2E1 (*c1/*c1), ALDH2 (*1/*2) and ADH1B (*1/*1) genotype frequencies were higher among patients with squamous cell carcinomas, at a level close to statistical significance (P = 0.014; P = 0.094; P = 0.0001 respectively). There were synergistic interactions among alcohol drinking and ALDH2, ADH1B and CYP2E1 genotypes. The risk of the ESCC in moderate-to-heavy drinkers with an inactive ALDH2 encoded by ALDH2*1/*2 as well as ADH1B encoded by ADH1B *1/*1 and CYP2EI encoded by CYP2EI *c1/*c1 was higher than that in the never/rare-to-light drinkers with an active ALDH2 (*1/*1 genotype) as well as ADH1B (*1/*2 + *2/*2) and CYP2E1 (*c1/*c2 + *c2/*c2) genotypes, with a statistically significant difference; ORs (95% CI) of 8.58 (3.28-22.68), 27.12 (8.52-70.19) and 7.64 (2.82-11.31) respectively. The risk of the ESCC in moderate-to-heavy drinkers with ALDH2 (*1/*2) combined the ADH1B (*1/*1) genotype or ALDH2 (*1/*2) combined the CYP2E1 (*c1/*c1) genotype leads to synergistic interactions, higher than drinkers with ALDH2 (*1/*1) + ADH1B (*1/*2 + *2/*2), ALDH2 (*1/*1) + CYP2E1 (*c1/*c2 + *c2/*c2) respectively, ORs (95% CI) of 7.46 (3.28-18.32) and 6.82 (1.44-9.76) respectively. Individuals with the ADH1B combined the CYP2E1 genotype showed no synergistic interaction. CONCLUSION: In our study, we found that alcohol consumption and polymorphisms in the CYP2E1, ADH1B and ALDH2 genes are important risk factors for ESCC, and that there was a synergistic interaction among polymorphisms in the CYP2E1, ALDH2 and ADH1B genes and heavy alcohol drinking, in Chinese males living in Gansu province, China. (c) 2008 WJG. All rights reserved. |
学科主题 | Gastroenterology & Hepatology |
出版地 | BEIJING |
语种 | 英语 |
WOS记录号 | WOS:000253866400024 |
内容类型 | 期刊论文 |
源URL | [http://ir.lzu.edu.cn/handle/262010/125663] |
专题 | 第一临床医学院_期刊论文 |
通讯作者 | Guo, YM (reprint author), Gansu Coll Tradit Chinese Med, Dept Clin Med, Lanzhou 730000, Gansu, Peoples R China. |
推荐引用方式 GB/T 7714 | Guo, YM,Wang, Q,Liu, YZ,et al. Genetic polymorphisms in cytochrome P4502E1, alcohol and aldehyde dehydrogenases and the risk of esophageal squamous cell carcinoma in Gansu Chinese males[J]. WORLD JOURNAL OF GASTROENTEROLOGY,2008,14(9):1444-1449. |
APA | Guo, YM.,Wang, Q.,Liu, YZ.,Chen, HM.,Qi, Z.,...&Guo, YM .(2008).Genetic polymorphisms in cytochrome P4502E1, alcohol and aldehyde dehydrogenases and the risk of esophageal squamous cell carcinoma in Gansu Chinese males.WORLD JOURNAL OF GASTROENTEROLOGY,14(9),1444-1449. |
MLA | Guo, YM,et al."Genetic polymorphisms in cytochrome P4502E1, alcohol and aldehyde dehydrogenases and the risk of esophageal squamous cell carcinoma in Gansu Chinese males".WORLD JOURNAL OF GASTROENTEROLOGY 14.9(2008):1444-1449. |
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