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ADH1C Ile350Val Polymorphism and Cancer Risk: Evidence from 35 Case–Control Studies
BACKGROUND: Alcohol dehydrogenase 1C (ADH1C) is the key enzyme catalyze oxidation of alcohol to acetaldehyde, which plays vital roles in the etiology of various cancer. To date, studies investigated the association between a functional polymorphism in ADH1C, Ile350Val (rs698), and risk of cancer hav...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3366713/ https://www.ncbi.nlm.nih.gov/pubmed/22675424 http://dx.doi.org/10.1371/journal.pone.0037227 |
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author | Xue, Yao Wang, Meilin Zhong, Dongyan Tong, Na Chu, Haiyan Sheng, Xiaojing Zhang, Zhengdong |
author_facet | Xue, Yao Wang, Meilin Zhong, Dongyan Tong, Na Chu, Haiyan Sheng, Xiaojing Zhang, Zhengdong |
author_sort | Xue, Yao |
collection | PubMed |
description | BACKGROUND: Alcohol dehydrogenase 1C (ADH1C) is the key enzyme catalyze oxidation of alcohol to acetaldehyde, which plays vital roles in the etiology of various cancer. To date, studies investigated the association between a functional polymorphism in ADH1C, Ile350Val (rs698), and risk of cancer have shown inclusive results. METHODS: A meta-analysis based on 35 case-control studies was performed to address this issue. Odds ratios (OR) with 95% confidence intervals (CIs) were used to assess the association. The statistical heterogeneity across studies was examined with χ2-based Q-test. RESULTS: Overall, no significant associations between ADH1C Ile350Val polymorphism and cancer risk were observed in any genetic models (P>0.05). In the stratified analyses, there was a significantly increased cancer risk among African (Val/Val vs. Ile/Ile OR = 2.19, 95% CI = 1.29−3.73, P (heterogeneity) = 0.989; Ile/Val + Val/Val vs. Ile/Ile: OR = 1.79, 95%CI = 1.18−2.71, P (heterogeneity) = 0.761; Val/Val vs. Ile/Val + Ile/Ile: OR = 1.92, 95% CI = 1.16−3.17, P (heterogeneity) = 0.981) and Asian (Ile/Val vs. Ile/Ile: OR = 1.58, 95% CI = 1.32−1.90, P (heterogeneity) = 0.375; Val/Val vs. Ile/Ile: OR = 3.84, 95% CI = 1.74−8.49, P (heterogeneity) = 0.160; Ile/Val + Val/Val vs. Ile/Ile: OR = 1.65, 95% CI = 1.38−1.96, P (heterogeneity) = 0.330; Val/Val vs. Ile/Val + Ile/Ile: OR = 3.54, 95% CI = 1.62−7.75, P (heterogeneity) = 0.154) studies. CONCLUSIONS: The results indicate that ADH1C Ile350Val polymorphism may contribute to cancer risk among Africans and Asians. Additional comprehensive system analyses are required to validate this association combined with other related polymorphisms. |
format | Online Article Text |
id | pubmed-3366713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33667132012-06-06 ADH1C Ile350Val Polymorphism and Cancer Risk: Evidence from 35 Case–Control Studies Xue, Yao Wang, Meilin Zhong, Dongyan Tong, Na Chu, Haiyan Sheng, Xiaojing Zhang, Zhengdong PLoS One Research Article BACKGROUND: Alcohol dehydrogenase 1C (ADH1C) is the key enzyme catalyze oxidation of alcohol to acetaldehyde, which plays vital roles in the etiology of various cancer. To date, studies investigated the association between a functional polymorphism in ADH1C, Ile350Val (rs698), and risk of cancer have shown inclusive results. METHODS: A meta-analysis based on 35 case-control studies was performed to address this issue. Odds ratios (OR) with 95% confidence intervals (CIs) were used to assess the association. The statistical heterogeneity across studies was examined with χ2-based Q-test. RESULTS: Overall, no significant associations between ADH1C Ile350Val polymorphism and cancer risk were observed in any genetic models (P>0.05). In the stratified analyses, there was a significantly increased cancer risk among African (Val/Val vs. Ile/Ile OR = 2.19, 95% CI = 1.29−3.73, P (heterogeneity) = 0.989; Ile/Val + Val/Val vs. Ile/Ile: OR = 1.79, 95%CI = 1.18−2.71, P (heterogeneity) = 0.761; Val/Val vs. Ile/Val + Ile/Ile: OR = 1.92, 95% CI = 1.16−3.17, P (heterogeneity) = 0.981) and Asian (Ile/Val vs. Ile/Ile: OR = 1.58, 95% CI = 1.32−1.90, P (heterogeneity) = 0.375; Val/Val vs. Ile/Ile: OR = 3.84, 95% CI = 1.74−8.49, P (heterogeneity) = 0.160; Ile/Val + Val/Val vs. Ile/Ile: OR = 1.65, 95% CI = 1.38−1.96, P (heterogeneity) = 0.330; Val/Val vs. Ile/Val + Ile/Ile: OR = 3.54, 95% CI = 1.62−7.75, P (heterogeneity) = 0.154) studies. CONCLUSIONS: The results indicate that ADH1C Ile350Val polymorphism may contribute to cancer risk among Africans and Asians. Additional comprehensive system analyses are required to validate this association combined with other related polymorphisms. Public Library of Science 2012-05-18 /pmc/articles/PMC3366713/ /pubmed/22675424 http://dx.doi.org/10.1371/journal.pone.0037227 Text en Xue et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Xue, Yao Wang, Meilin Zhong, Dongyan Tong, Na Chu, Haiyan Sheng, Xiaojing Zhang, Zhengdong ADH1C Ile350Val Polymorphism and Cancer Risk: Evidence from 35 Case–Control Studies |
title |
ADH1C Ile350Val Polymorphism and Cancer Risk: Evidence from 35 Case–Control Studies |
title_full |
ADH1C Ile350Val Polymorphism and Cancer Risk: Evidence from 35 Case–Control Studies |
title_fullStr |
ADH1C Ile350Val Polymorphism and Cancer Risk: Evidence from 35 Case–Control Studies |
title_full_unstemmed |
ADH1C Ile350Val Polymorphism and Cancer Risk: Evidence from 35 Case–Control Studies |
title_short |
ADH1C Ile350Val Polymorphism and Cancer Risk: Evidence from 35 Case–Control Studies |
title_sort | adh1c ile350val polymorphism and cancer risk: evidence from 35 case–control studies |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3366713/ https://www.ncbi.nlm.nih.gov/pubmed/22675424 http://dx.doi.org/10.1371/journal.pone.0037227 |
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