Relationship between genetic polymorphisms of alcohol and aldehyde dehydrogenases and esophageal squamous cell carcinoma risk in males
Journal
World Journal of Gastroenterology
Journal Volume
11
Journal Issue
33
Pages
5103-5108
Date Issued
2005
Author(s)
Abstract
Aim: To investigate the association between the genetic polymorphisms of ADH2 and ALDH2, lifetime alcohol consumption and esophageal cancer risk in the Taiwanese men. Methods: Between August 2000 and June 2003, 134 pathologically-proven esophageal squamous cell carcinoma male patients and 237 male controls were recruited from Kaohsiung Medical University Hospital and Kaohsiung Veterans General Hospital in southern Taiwan. ADH2 and ALDH2 polymorphisms were genotyped using PCR-RFLP. Results: Compared to those with ADH2*2/*2, individuals with ADH2*1/*2 and ADH2*1/*1 had 2.28-and 7.14-fold, respectively, increased risk of developing esophageal cancer (95%CI = 1.11-4.68 and 2.76-18.46) after adjusting for alcohol consumption and other covariates. The significant increased risk was also noted among subjects with ALDH2*1/*2 (adjusted OR (AOR) = 5.25, 95%CI = 2.47-11.19), when compared to those with ALDH2*1/*1. The increased risk of esophageal cancer was made greater, when subjects carried both ADH2*1/*1 and ALDH2*1/*2, compared to those with ADH2*1/*2 or ADH2*2/*2 and ALDH2*1/*1 (AOR = 36.79, 95%CI = 9.36-144.65). Furthermore, we found a multiplicative effect of lifetime alcoholic consumption and genotypes (ADH2 and ALDH2) on esophageal cancer risk. Conclusion: Our findings suggest that polymorphisms of ADH2 and ALDH2 can modify the influence of alcoholic consumption on esophageal cancer risk. ? 2005 The WJG Press and Elsevier Inc. All rights reserved.
Subjects
Alcohol; Alcohol dehydrogenase; Aldehyde dehydrogenase; Esophageal cancer; Genetic polymorphisms
SDGs
Other Subjects
alcohol dehydrogenase; aldehyde dehydrogenase; adult; aged; alcohol consumption; article; cancer risk; carcinogenesis; controlled study; covariance; esophageal squamous cell carcinoma; general hospital; genetic polymorphism; genotype; human; individuality; major clinical study; male; molecular phylogeny; polymerase chain reaction; restriction fragment length polymorphism; Taiwan; university hospital
Type
journal article