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Association between Glutathione S-Transferase T1 Null Genotype and Gastric Cancer Risk: A Meta-Analysis of 48 Studies
BACKGROUND: Glutathione S-transferases (GSTs) have proved to be involved in the detoxifying several carcinogens and may play an important role in carcinogenesis of cancer. Previous studies on the association between Glutathione S-transferase T1 (GSTT1) polymorphism and gastric cancer risk reported i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3621870/ https://www.ncbi.nlm.nih.gov/pubmed/23585855 http://dx.doi.org/10.1371/journal.pone.0060833 |
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author | Ma, Weiyuan Zhuang, Le Han, Bo Tang, Bo |
author_facet | Ma, Weiyuan Zhuang, Le Han, Bo Tang, Bo |
author_sort | Ma, Weiyuan |
collection | PubMed |
description | BACKGROUND: Glutathione S-transferases (GSTs) have proved to be involved in the detoxifying several carcinogens and may play an important role in carcinogenesis of cancer. Previous studies on the association between Glutathione S-transferase T1 (GSTT1) polymorphism and gastric cancer risk reported inconclusive results. To clarify the possible association, we conducted a meta-analysis of eligible studies. METHODS: We searched in the Pubmed, Embase, and Wangfang Medicine databases for studies assessing the association between GSTT1 null genotype and gastric cancer risk. The pooled odds ratio (OR) and its 95% confidence interval (95%CI) was calculated to assess the strength of the association. A total of 48 studies with a total of 24,440 individuals were ultimately eligible for meta-analysis. RESULTS: Overall, GSTT1 null genotype was significantly associated with increased risk of gastric cancer (Random-effect OR = 1.23, 95%CI 1.13–1.35, P (OR) <0.001, I(2) = 45.5%). Significant association was also found in Caucasians, East Asians, and Indians (P (Caucasians) = 0.010; P (East Asians) = 0.003; P (Indians) = 0.017). After adjusting for other confounding variables, GSTT1 null genotype was also significantly associated with increased risk of gastric cancer (Random-effect OR = 1.43, 95%CI 1.20–1.71, P (OR) <0.001, I(2) = 48.1%). CONCLUSION: The meta-analysis provides strong evidence for the significant association between GSTT1 null genotype and increased risk of gastric cancer. |
format | Online Article Text |
id | pubmed-3621870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36218702013-04-12 Association between Glutathione S-Transferase T1 Null Genotype and Gastric Cancer Risk: A Meta-Analysis of 48 Studies Ma, Weiyuan Zhuang, Le Han, Bo Tang, Bo PLoS One Research Article BACKGROUND: Glutathione S-transferases (GSTs) have proved to be involved in the detoxifying several carcinogens and may play an important role in carcinogenesis of cancer. Previous studies on the association between Glutathione S-transferase T1 (GSTT1) polymorphism and gastric cancer risk reported inconclusive results. To clarify the possible association, we conducted a meta-analysis of eligible studies. METHODS: We searched in the Pubmed, Embase, and Wangfang Medicine databases for studies assessing the association between GSTT1 null genotype and gastric cancer risk. The pooled odds ratio (OR) and its 95% confidence interval (95%CI) was calculated to assess the strength of the association. A total of 48 studies with a total of 24,440 individuals were ultimately eligible for meta-analysis. RESULTS: Overall, GSTT1 null genotype was significantly associated with increased risk of gastric cancer (Random-effect OR = 1.23, 95%CI 1.13–1.35, P (OR) <0.001, I(2) = 45.5%). Significant association was also found in Caucasians, East Asians, and Indians (P (Caucasians) = 0.010; P (East Asians) = 0.003; P (Indians) = 0.017). After adjusting for other confounding variables, GSTT1 null genotype was also significantly associated with increased risk of gastric cancer (Random-effect OR = 1.43, 95%CI 1.20–1.71, P (OR) <0.001, I(2) = 48.1%). CONCLUSION: The meta-analysis provides strong evidence for the significant association between GSTT1 null genotype and increased risk of gastric cancer. Public Library of Science 2013-04-09 /pmc/articles/PMC3621870/ /pubmed/23585855 http://dx.doi.org/10.1371/journal.pone.0060833 Text en © 2013 Ma 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 Ma, Weiyuan Zhuang, Le Han, Bo Tang, Bo Association between Glutathione S-Transferase T1 Null Genotype and Gastric Cancer Risk: A Meta-Analysis of 48 Studies |
title | Association between Glutathione S-Transferase T1 Null Genotype and Gastric Cancer Risk: A Meta-Analysis of 48 Studies |
title_full | Association between Glutathione S-Transferase T1 Null Genotype and Gastric Cancer Risk: A Meta-Analysis of 48 Studies |
title_fullStr | Association between Glutathione S-Transferase T1 Null Genotype and Gastric Cancer Risk: A Meta-Analysis of 48 Studies |
title_full_unstemmed | Association between Glutathione S-Transferase T1 Null Genotype and Gastric Cancer Risk: A Meta-Analysis of 48 Studies |
title_short | Association between Glutathione S-Transferase T1 Null Genotype and Gastric Cancer Risk: A Meta-Analysis of 48 Studies |
title_sort | association between glutathione s-transferase t1 null genotype and gastric cancer risk: a meta-analysis of 48 studies |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3621870/ https://www.ncbi.nlm.nih.gov/pubmed/23585855 http://dx.doi.org/10.1371/journal.pone.0060833 |
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