Cargando…
The Glutathione S-Transferase P1 341C>T Polymorphism and Cancer Risk: A Meta-Analysis of 28 Case-Control Studies
BACKGROUND: GSTP1, which is one major group of the glutathione S-transferase family, plays an important role in the metabolism of carcinogens and toxins, reducing damage of DNA as a suppressor of carcinogenesis. The 341C>T polymorphism of the GSTP1 has been implicated in cancer risk through cutti...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3578943/ https://www.ncbi.nlm.nih.gov/pubmed/23437223 http://dx.doi.org/10.1371/journal.pone.0056722 |
_version_ | 1782260067706339328 |
---|---|
author | Huang, Sheng-xin Wu, Fei-xiang Luo, Min Ma, Liang Gao, Ke-feng Li, Jian Wu, Wen-juan Huang, Shan Yang, Qi Liu, Ke Zhao, Yin-nong Li, Le-qun |
author_facet | Huang, Sheng-xin Wu, Fei-xiang Luo, Min Ma, Liang Gao, Ke-feng Li, Jian Wu, Wen-juan Huang, Shan Yang, Qi Liu, Ke Zhao, Yin-nong Li, Le-qun |
author_sort | Huang, Sheng-xin |
collection | PubMed |
description | BACKGROUND: GSTP1, which is one major group of the glutathione S-transferase family, plays an important role in the metabolism of carcinogens and toxins, reducing damage of DNA as a suppressor of carcinogenesis. The 341C>T polymorphism of the GSTP1 has been implicated in cancer risk through cutting down its metabolic detoxification activities. However, results from previous studies remain conflicting rather than conclusive. To clarify the correlation and provide more statistical evidence for detecting the significance of 341C>T, a meta-analysis was conducted. METHODOLOGY/PRINCIPAL FINDINGS: The relevant studies were identified through searching of PubMed, Embase, ISI Web of Knowledge and China National Knowledge Infrastructure in August 2012, and selected based on the established inclusion criteria for publications, then a meta-analysis was performed to quantitatively summarize the association of GSTP1 341C>T polymorphism with cancer susceptibility. Stratified analyses were employed to identify the source of heterogeneity. Publication bias was evaluated as well as sensitivity analysis. Based on 28 case-control studies with 13249 cases and 16798 controls, the pooled results indicated that the variant genotypes significantly increased the risk of cancer in homozygote comparison (TT versus CC: P = 0.012, OR = 1.40, 95% CI: 1.08–1.81, P (het.) = 0.575), and recessive model (TT versus CT/CC: P = 0.012, OR = 1.40, 95% CI: 1.08–1.81, P (het.) = 0.562). This was confirmed when stratified analyses were conducted according to ethnicity, source of control, matched control, quality score and cancer types. Moreover, significantly increased risk of cancer was also found in lung cancer (heterozygote comparison and dominant model). The stability of these observations was confirmed by a sensitivity analysis. Begger's funnel plot and Egger's test did not reveal any publication bias. CONCLUSIONS/SIGNIFICANCE: This meta-analysis suggests that the GSTP1 341C>T polymorphism may contribute to genetic susceptibility to cancer, especially to lung cancer, and in Asian population. Nevertheless, additional well-designed studies focusing on different ethnicity and cancer types are needed to provide a more exact and comprehensive conclusion. |
format | Online Article Text |
id | pubmed-3578943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35789432013-02-22 The Glutathione S-Transferase P1 341C>T Polymorphism and Cancer Risk: A Meta-Analysis of 28 Case-Control Studies Huang, Sheng-xin Wu, Fei-xiang Luo, Min Ma, Liang Gao, Ke-feng Li, Jian Wu, Wen-juan Huang, Shan Yang, Qi Liu, Ke Zhao, Yin-nong Li, Le-qun PLoS One Research Article BACKGROUND: GSTP1, which is one major group of the glutathione S-transferase family, plays an important role in the metabolism of carcinogens and toxins, reducing damage of DNA as a suppressor of carcinogenesis. The 341C>T polymorphism of the GSTP1 has been implicated in cancer risk through cutting down its metabolic detoxification activities. However, results from previous studies remain conflicting rather than conclusive. To clarify the correlation and provide more statistical evidence for detecting the significance of 341C>T, a meta-analysis was conducted. METHODOLOGY/PRINCIPAL FINDINGS: The relevant studies were identified through searching of PubMed, Embase, ISI Web of Knowledge and China National Knowledge Infrastructure in August 2012, and selected based on the established inclusion criteria for publications, then a meta-analysis was performed to quantitatively summarize the association of GSTP1 341C>T polymorphism with cancer susceptibility. Stratified analyses were employed to identify the source of heterogeneity. Publication bias was evaluated as well as sensitivity analysis. Based on 28 case-control studies with 13249 cases and 16798 controls, the pooled results indicated that the variant genotypes significantly increased the risk of cancer in homozygote comparison (TT versus CC: P = 0.012, OR = 1.40, 95% CI: 1.08–1.81, P (het.) = 0.575), and recessive model (TT versus CT/CC: P = 0.012, OR = 1.40, 95% CI: 1.08–1.81, P (het.) = 0.562). This was confirmed when stratified analyses were conducted according to ethnicity, source of control, matched control, quality score and cancer types. Moreover, significantly increased risk of cancer was also found in lung cancer (heterozygote comparison and dominant model). The stability of these observations was confirmed by a sensitivity analysis. Begger's funnel plot and Egger's test did not reveal any publication bias. CONCLUSIONS/SIGNIFICANCE: This meta-analysis suggests that the GSTP1 341C>T polymorphism may contribute to genetic susceptibility to cancer, especially to lung cancer, and in Asian population. Nevertheless, additional well-designed studies focusing on different ethnicity and cancer types are needed to provide a more exact and comprehensive conclusion. Public Library of Science 2013-02-21 /pmc/articles/PMC3578943/ /pubmed/23437223 http://dx.doi.org/10.1371/journal.pone.0056722 Text en © 2013 Huang 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 Huang, Sheng-xin Wu, Fei-xiang Luo, Min Ma, Liang Gao, Ke-feng Li, Jian Wu, Wen-juan Huang, Shan Yang, Qi Liu, Ke Zhao, Yin-nong Li, Le-qun The Glutathione S-Transferase P1 341C>T Polymorphism and Cancer Risk: A Meta-Analysis of 28 Case-Control Studies |
title | The Glutathione S-Transferase P1 341C>T Polymorphism and Cancer Risk: A Meta-Analysis of 28 Case-Control Studies |
title_full | The Glutathione S-Transferase P1 341C>T Polymorphism and Cancer Risk: A Meta-Analysis of 28 Case-Control Studies |
title_fullStr | The Glutathione S-Transferase P1 341C>T Polymorphism and Cancer Risk: A Meta-Analysis of 28 Case-Control Studies |
title_full_unstemmed | The Glutathione S-Transferase P1 341C>T Polymorphism and Cancer Risk: A Meta-Analysis of 28 Case-Control Studies |
title_short | The Glutathione S-Transferase P1 341C>T Polymorphism and Cancer Risk: A Meta-Analysis of 28 Case-Control Studies |
title_sort | glutathione s-transferase p1 341c>t polymorphism and cancer risk: a meta-analysis of 28 case-control studies |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3578943/ https://www.ncbi.nlm.nih.gov/pubmed/23437223 http://dx.doi.org/10.1371/journal.pone.0056722 |
work_keys_str_mv | AT huangshengxin theglutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT wufeixiang theglutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT luomin theglutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT maliang theglutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT gaokefeng theglutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT lijian theglutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT wuwenjuan theglutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT huangshan theglutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT yangqi theglutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT liuke theglutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT zhaoyinnong theglutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT lilequn theglutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT huangshengxin glutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT wufeixiang glutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT luomin glutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT maliang glutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT gaokefeng glutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT lijian glutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT wuwenjuan glutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT huangshan glutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT yangqi glutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT liuke glutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT zhaoyinnong glutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies AT lilequn glutathionestransferasep1341ctpolymorphismandcancerriskametaanalysisof28casecontrolstudies |