Cargando…
Association of GST Genetic Polymorphisms with the Susceptibility to Hepatocellular Carcinoma (HCC) in Chinese Population Evaluated by an Updated Systematic Meta-Analysis
BACKGROUND: Due to the possible involvement of Glutathione S-transferase Mu-1 (GSTM1) and Glutathione S-transferase theta-1 (GSTT1) in the detoxification of environmental carcinogens, environmental toxins, and oxidative stress products, genetic polymorphisms of these two genes may play important rol...
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/PMC3577765/ https://www.ncbi.nlm.nih.gov/pubmed/23437305 http://dx.doi.org/10.1371/journal.pone.0057043 |
_version_ | 1782259966754684928 |
---|---|
author | Liu, Kui Zhang, Lu Lin, Xialu Chen, Liangliang Shi, Hongbo Magaye, Ruth Zou, Baobo Zhao, Jinshun |
author_facet | Liu, Kui Zhang, Lu Lin, Xialu Chen, Liangliang Shi, Hongbo Magaye, Ruth Zou, Baobo Zhao, Jinshun |
author_sort | Liu, Kui |
collection | PubMed |
description | BACKGROUND: Due to the possible involvement of Glutathione S-transferase Mu-1 (GSTM1) and Glutathione S-transferase theta-1 (GSTT1) in the detoxification of environmental carcinogens, environmental toxins, and oxidative stress products, genetic polymorphisms of these two genes may play important roles in the susceptibility of human being to hepatocellular carcinoma. However, the existing research results are not conclusive. METHODS: A systematic literature search using databases (PubMed, Scopus, Embase, Chinese Biomedical Database, Chinese National Knowledge Infrastructure, Wanfang Data, etc.) for the eligible studies meeting the inclusion criteria including case-control studies or cohort studies is evaluated using an updated systematic meta-analysis. RESULTS: Significant increase in the risk of HCC in the Chinese population is found in GSTM1 null genotype (OR = 1.47, 95% CI: 1.21 to 1.79, P<0.001) and GSTT1 null genotype (OR = 1.38, 95% CI: 1.14 to 1.65, P<0.001). Analysis using the random-effects model found an increased risk of HCC in GSTM1-GSTT1 dual null population (OR = 1.79, 95% CI: 1.26 to 2.53, P<0.001). In addition, subgroup analyses showed a significant increase in the association of GST genetic polymorphisms (GSTM1, GSTT1, and GSTM1-GSTT1) with HCC in southeast and central China mainland. However, available data collected by this study fail to show an association between GST genetic polymorphisms and HCC in people from the Taiwan region (for GSTM1: OR = 0.78, 95% CI: 0.60 to 1.01, P = 0.06; for GSTT1: OR = 0.94, 95% CI: 0.78 to 1.14, P = 0.546; for GSTM1-GSTT1: OR = 1.04, 95% CI: 0.81 to 1.32, P = 0.77). Sensitivity analysis and publication bias diagnostics confirmed the reliability and stability of this meta-analysis. CONCLUSIONS: Our results indicate that both GSTM1 and GSTT1 null genotypes are associated with an increased HCC risk in Chinese population. Peoples with dual null genotypes of GSTM1-GSTT1 are more susceptible to developing HCC. In conclusion, GST genetic polymorphisms play vital roles in the development of HCC in the Chinese population. |
format | Online Article Text |
id | pubmed-3577765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35777652013-02-22 Association of GST Genetic Polymorphisms with the Susceptibility to Hepatocellular Carcinoma (HCC) in Chinese Population Evaluated by an Updated Systematic Meta-Analysis Liu, Kui Zhang, Lu Lin, Xialu Chen, Liangliang Shi, Hongbo Magaye, Ruth Zou, Baobo Zhao, Jinshun PLoS One Research Article BACKGROUND: Due to the possible involvement of Glutathione S-transferase Mu-1 (GSTM1) and Glutathione S-transferase theta-1 (GSTT1) in the detoxification of environmental carcinogens, environmental toxins, and oxidative stress products, genetic polymorphisms of these two genes may play important roles in the susceptibility of human being to hepatocellular carcinoma. However, the existing research results are not conclusive. METHODS: A systematic literature search using databases (PubMed, Scopus, Embase, Chinese Biomedical Database, Chinese National Knowledge Infrastructure, Wanfang Data, etc.) for the eligible studies meeting the inclusion criteria including case-control studies or cohort studies is evaluated using an updated systematic meta-analysis. RESULTS: Significant increase in the risk of HCC in the Chinese population is found in GSTM1 null genotype (OR = 1.47, 95% CI: 1.21 to 1.79, P<0.001) and GSTT1 null genotype (OR = 1.38, 95% CI: 1.14 to 1.65, P<0.001). Analysis using the random-effects model found an increased risk of HCC in GSTM1-GSTT1 dual null population (OR = 1.79, 95% CI: 1.26 to 2.53, P<0.001). In addition, subgroup analyses showed a significant increase in the association of GST genetic polymorphisms (GSTM1, GSTT1, and GSTM1-GSTT1) with HCC in southeast and central China mainland. However, available data collected by this study fail to show an association between GST genetic polymorphisms and HCC in people from the Taiwan region (for GSTM1: OR = 0.78, 95% CI: 0.60 to 1.01, P = 0.06; for GSTT1: OR = 0.94, 95% CI: 0.78 to 1.14, P = 0.546; for GSTM1-GSTT1: OR = 1.04, 95% CI: 0.81 to 1.32, P = 0.77). Sensitivity analysis and publication bias diagnostics confirmed the reliability and stability of this meta-analysis. CONCLUSIONS: Our results indicate that both GSTM1 and GSTT1 null genotypes are associated with an increased HCC risk in Chinese population. Peoples with dual null genotypes of GSTM1-GSTT1 are more susceptible to developing HCC. In conclusion, GST genetic polymorphisms play vital roles in the development of HCC in the Chinese population. Public Library of Science 2013-02-20 /pmc/articles/PMC3577765/ /pubmed/23437305 http://dx.doi.org/10.1371/journal.pone.0057043 Text en © 2013 Liu 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 Liu, Kui Zhang, Lu Lin, Xialu Chen, Liangliang Shi, Hongbo Magaye, Ruth Zou, Baobo Zhao, Jinshun Association of GST Genetic Polymorphisms with the Susceptibility to Hepatocellular Carcinoma (HCC) in Chinese Population Evaluated by an Updated Systematic Meta-Analysis |
title | Association of GST Genetic Polymorphisms with the Susceptibility to Hepatocellular Carcinoma (HCC) in Chinese Population Evaluated by an Updated Systematic Meta-Analysis |
title_full | Association of GST Genetic Polymorphisms with the Susceptibility to Hepatocellular Carcinoma (HCC) in Chinese Population Evaluated by an Updated Systematic Meta-Analysis |
title_fullStr | Association of GST Genetic Polymorphisms with the Susceptibility to Hepatocellular Carcinoma (HCC) in Chinese Population Evaluated by an Updated Systematic Meta-Analysis |
title_full_unstemmed | Association of GST Genetic Polymorphisms with the Susceptibility to Hepatocellular Carcinoma (HCC) in Chinese Population Evaluated by an Updated Systematic Meta-Analysis |
title_short | Association of GST Genetic Polymorphisms with the Susceptibility to Hepatocellular Carcinoma (HCC) in Chinese Population Evaluated by an Updated Systematic Meta-Analysis |
title_sort | association of gst genetic polymorphisms with the susceptibility to hepatocellular carcinoma (hcc) in chinese population evaluated by an updated systematic meta-analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3577765/ https://www.ncbi.nlm.nih.gov/pubmed/23437305 http://dx.doi.org/10.1371/journal.pone.0057043 |
work_keys_str_mv | AT liukui associationofgstgeneticpolymorphismswiththesusceptibilitytohepatocellularcarcinomahccinchinesepopulationevaluatedbyanupdatedsystematicmetaanalysis AT zhanglu associationofgstgeneticpolymorphismswiththesusceptibilitytohepatocellularcarcinomahccinchinesepopulationevaluatedbyanupdatedsystematicmetaanalysis AT linxialu associationofgstgeneticpolymorphismswiththesusceptibilitytohepatocellularcarcinomahccinchinesepopulationevaluatedbyanupdatedsystematicmetaanalysis AT chenliangliang associationofgstgeneticpolymorphismswiththesusceptibilitytohepatocellularcarcinomahccinchinesepopulationevaluatedbyanupdatedsystematicmetaanalysis AT shihongbo associationofgstgeneticpolymorphismswiththesusceptibilitytohepatocellularcarcinomahccinchinesepopulationevaluatedbyanupdatedsystematicmetaanalysis AT magayeruth associationofgstgeneticpolymorphismswiththesusceptibilitytohepatocellularcarcinomahccinchinesepopulationevaluatedbyanupdatedsystematicmetaanalysis AT zoubaobo associationofgstgeneticpolymorphismswiththesusceptibilitytohepatocellularcarcinomahccinchinesepopulationevaluatedbyanupdatedsystematicmetaanalysis AT zhaojinshun associationofgstgeneticpolymorphismswiththesusceptibilitytohepatocellularcarcinomahccinchinesepopulationevaluatedbyanupdatedsystematicmetaanalysis |