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Association between alcohol dehydrogenase-2 gene polymorphism and esophageal cancer risk: a meta-analysis

BACKGROUND: It has been shown that gene polymorphisms may play an important role in the carcinogenesis of esophageal cancer. This study is to investigate the role of alcohol dehydrogenase 1B (ADH1B) gene Arg47His polymorphism in esophageal cancer susceptibility. METHODS: Case-control studies publish...

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Autores principales: Mao, Ning, Nie, Siyao, Hong, Bin, Li, Chao, Shen, Xueyuan, Xiong, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4957421/
https://www.ncbi.nlm.nih.gov/pubmed/27450204
http://dx.doi.org/10.1186/s12957-016-0937-y
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author Mao, Ning
Nie, Siyao
Hong, Bin
Li, Chao
Shen, Xueyuan
Xiong, Tao
author_facet Mao, Ning
Nie, Siyao
Hong, Bin
Li, Chao
Shen, Xueyuan
Xiong, Tao
author_sort Mao, Ning
collection PubMed
description BACKGROUND: It has been shown that gene polymorphisms may play an important role in the carcinogenesis of esophageal cancer. This study is to investigate the role of alcohol dehydrogenase 1B (ADH1B) gene Arg47His polymorphism in esophageal cancer susceptibility. METHODS: Case-control studies published between January 2000 and June 2015 were searched to retrieve relevant articles. The pooled odds ratio (OR) and 95 % confidence interval (CI) were employed to calculate the strength of association. RESULTS: A total of 23 relevant articles were finally selected for the analysis, including 9338 esophageal cancer patients and 14,896 matched controls. Overall, we found that the 47His allele was significant associated with the decreased risk of esophageal cancer when compared with the 47Arg allele in total populations (A vs. G: OR = 0.67, 95 % CI = 0.59–0.76, P < 0.00001). This protective relationship was observed under other genetic models as well (P < 0.00001). Subgroup analysis by ethnicity showed that ADH1B Arg47His variant was associated with the decreased esophageal cancer risk under all the genetic models (P < 0.00001) among Asians, especially in Chinese and Japanese; while in non-Asians, no significant correlation was detected in any genetic models (P > 0.05). Furthermore, Arg/Arg genotype of ADH1B Arg47His variant combined with drinking, smoking and males appeared to show a high risk in patients with esophageal cancer. CONCLUSIONS: Our results suggested that ADH1B gene Arg47His variant was associated with the decreased esophageal cancer risk. Genetic-environmental interaction should be further considered in the future researches.
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spelling pubmed-49574212016-07-23 Association between alcohol dehydrogenase-2 gene polymorphism and esophageal cancer risk: a meta-analysis Mao, Ning Nie, Siyao Hong, Bin Li, Chao Shen, Xueyuan Xiong, Tao World J Surg Oncol Research BACKGROUND: It has been shown that gene polymorphisms may play an important role in the carcinogenesis of esophageal cancer. This study is to investigate the role of alcohol dehydrogenase 1B (ADH1B) gene Arg47His polymorphism in esophageal cancer susceptibility. METHODS: Case-control studies published between January 2000 and June 2015 were searched to retrieve relevant articles. The pooled odds ratio (OR) and 95 % confidence interval (CI) were employed to calculate the strength of association. RESULTS: A total of 23 relevant articles were finally selected for the analysis, including 9338 esophageal cancer patients and 14,896 matched controls. Overall, we found that the 47His allele was significant associated with the decreased risk of esophageal cancer when compared with the 47Arg allele in total populations (A vs. G: OR = 0.67, 95 % CI = 0.59–0.76, P < 0.00001). This protective relationship was observed under other genetic models as well (P < 0.00001). Subgroup analysis by ethnicity showed that ADH1B Arg47His variant was associated with the decreased esophageal cancer risk under all the genetic models (P < 0.00001) among Asians, especially in Chinese and Japanese; while in non-Asians, no significant correlation was detected in any genetic models (P > 0.05). Furthermore, Arg/Arg genotype of ADH1B Arg47His variant combined with drinking, smoking and males appeared to show a high risk in patients with esophageal cancer. CONCLUSIONS: Our results suggested that ADH1B gene Arg47His variant was associated with the decreased esophageal cancer risk. Genetic-environmental interaction should be further considered in the future researches. BioMed Central 2016-07-22 /pmc/articles/PMC4957421/ /pubmed/27450204 http://dx.doi.org/10.1186/s12957-016-0937-y Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Mao, Ning
Nie, Siyao
Hong, Bin
Li, Chao
Shen, Xueyuan
Xiong, Tao
Association between alcohol dehydrogenase-2 gene polymorphism and esophageal cancer risk: a meta-analysis
title Association between alcohol dehydrogenase-2 gene polymorphism and esophageal cancer risk: a meta-analysis
title_full Association between alcohol dehydrogenase-2 gene polymorphism and esophageal cancer risk: a meta-analysis
title_fullStr Association between alcohol dehydrogenase-2 gene polymorphism and esophageal cancer risk: a meta-analysis
title_full_unstemmed Association between alcohol dehydrogenase-2 gene polymorphism and esophageal cancer risk: a meta-analysis
title_short Association between alcohol dehydrogenase-2 gene polymorphism and esophageal cancer risk: a meta-analysis
title_sort association between alcohol dehydrogenase-2 gene polymorphism and esophageal cancer risk: a meta-analysis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4957421/
https://www.ncbi.nlm.nih.gov/pubmed/27450204
http://dx.doi.org/10.1186/s12957-016-0937-y
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