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...

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Main Authors: Weiyuan Ma, Le Zhuang, Bo Han, Bo Tang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3621870?pdf=render
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spelling doaj-865d09ebcd60461a812d6598e085aa6e2020-11-25T02:45:39ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0184e6083310.1371/journal.pone.0060833Association between glutathione S-transferase T1 null genotype and gastric cancer risk: a meta-analysis of 48 studies.Weiyuan MaLe ZhuangBo HanBo TangBACKGROUND: 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.http://europepmc.org/articles/PMC3621870?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Weiyuan Ma
Le Zhuang
Bo Han
Bo Tang
spellingShingle Weiyuan Ma
Le Zhuang
Bo Han
Bo Tang
Association between glutathione S-transferase T1 null genotype and gastric cancer risk: a meta-analysis of 48 studies.
PLoS ONE
author_facet Weiyuan Ma
Le Zhuang
Bo Han
Bo Tang
author_sort Weiyuan Ma
title 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_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_sort association between glutathione s-transferase t1 null genotype and gastric cancer risk: a meta-analysis of 48 studies.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
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.
url http://europepmc.org/articles/PMC3621870?pdf=render
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AT bohan associationbetweenglutathionestransferaset1nullgenotypeandgastriccancerriskametaanalysisof48studies
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