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Clinical significance of ALDH2 rs671 polymorphism in esophageal cancer: evidence from 31 case-control studies
BACKGROUND: Aldehyde dehydrogenase 2 (ALDH2), a critical enzyme for the detoxification of alcohol, is associated with many types of cancers. To verify the relationship of ALDH2 rs671 G>A polymorphism and esophageal cancer (EC), we performed a meta-analysis of a total of 31 published data includin...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4376259/ https://www.ncbi.nlm.nih.gov/pubmed/25848305 http://dx.doi.org/10.2147/OTT.S76526 |
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author | Zhao, Tingting Wang, Chun Shen, Lili Gu, Dongying Xu, Zhi Zhang, Xunlei Xu, Yong Chen, Jinfei |
author_facet | Zhao, Tingting Wang, Chun Shen, Lili Gu, Dongying Xu, Zhi Zhang, Xunlei Xu, Yong Chen, Jinfei |
author_sort | Zhao, Tingting |
collection | PubMed |
description | BACKGROUND: Aldehyde dehydrogenase 2 (ALDH2), a critical enzyme for the detoxification of alcohol, is associated with many types of cancers. To verify the relationship of ALDH2 rs671 G>A polymorphism and esophageal cancer (EC), we performed a meta-analysis of a total of 31 published data including 8,510 patients and 16,197 controls. METHODS: The pooled odds ratio (OR) and the 95% confidence interval (CI) were calculated using a fixed or random-effects model. Heterogeneity (P(H)), publication bias, and sensitivity analysis were also determined. RESULTS: Although a protective effort was found in the rs671 homozygote comparison (AA/GG: OR=0.69; 95% CI=0.48–0.98), the heterozygote comparison was apparently associated with the risk of EC, particularly in the Chinese population (AG/GG: OR=1.39; 95% CI=1.03–1.87). Alcohol consumption remarkably increased this risk, especially in the AG genotype. Drinking men with the AG genotype appeared to show a higher risk (AG/GG: OR=4.39; 95% CI=1.24–6.55) than drinking women. CONCLUSION: The present meta-analysis provided advanced information regarding the association of the ALDH2 A>G polymorphism and EC. Taken together, insights from this study suggested an enhanced effect on the development of EC through a genetic–environmental interaction. |
format | Online Article Text |
id | pubmed-4376259 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43762592015-04-06 Clinical significance of ALDH2 rs671 polymorphism in esophageal cancer: evidence from 31 case-control studies Zhao, Tingting Wang, Chun Shen, Lili Gu, Dongying Xu, Zhi Zhang, Xunlei Xu, Yong Chen, Jinfei Onco Targets Ther Original Research BACKGROUND: Aldehyde dehydrogenase 2 (ALDH2), a critical enzyme for the detoxification of alcohol, is associated with many types of cancers. To verify the relationship of ALDH2 rs671 G>A polymorphism and esophageal cancer (EC), we performed a meta-analysis of a total of 31 published data including 8,510 patients and 16,197 controls. METHODS: The pooled odds ratio (OR) and the 95% confidence interval (CI) were calculated using a fixed or random-effects model. Heterogeneity (P(H)), publication bias, and sensitivity analysis were also determined. RESULTS: Although a protective effort was found in the rs671 homozygote comparison (AA/GG: OR=0.69; 95% CI=0.48–0.98), the heterozygote comparison was apparently associated with the risk of EC, particularly in the Chinese population (AG/GG: OR=1.39; 95% CI=1.03–1.87). Alcohol consumption remarkably increased this risk, especially in the AG genotype. Drinking men with the AG genotype appeared to show a higher risk (AG/GG: OR=4.39; 95% CI=1.24–6.55) than drinking women. CONCLUSION: The present meta-analysis provided advanced information regarding the association of the ALDH2 A>G polymorphism and EC. Taken together, insights from this study suggested an enhanced effect on the development of EC through a genetic–environmental interaction. Dove Medical Press 2015-03-23 /pmc/articles/PMC4376259/ /pubmed/25848305 http://dx.doi.org/10.2147/OTT.S76526 Text en © 2015 Zhao et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Zhao, Tingting Wang, Chun Shen, Lili Gu, Dongying Xu, Zhi Zhang, Xunlei Xu, Yong Chen, Jinfei Clinical significance of ALDH2 rs671 polymorphism in esophageal cancer: evidence from 31 case-control studies |
title | Clinical significance of ALDH2 rs671 polymorphism in esophageal cancer: evidence from 31 case-control studies |
title_full | Clinical significance of ALDH2 rs671 polymorphism in esophageal cancer: evidence from 31 case-control studies |
title_fullStr | Clinical significance of ALDH2 rs671 polymorphism in esophageal cancer: evidence from 31 case-control studies |
title_full_unstemmed | Clinical significance of ALDH2 rs671 polymorphism in esophageal cancer: evidence from 31 case-control studies |
title_short | Clinical significance of ALDH2 rs671 polymorphism in esophageal cancer: evidence from 31 case-control studies |
title_sort | clinical significance of aldh2 rs671 polymorphism in esophageal cancer: evidence from 31 case-control studies |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4376259/ https://www.ncbi.nlm.nih.gov/pubmed/25848305 http://dx.doi.org/10.2147/OTT.S76526 |
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