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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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 |
work_keys_str_mv |
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