Association of GSTM1 null allele with prostate cancer risk: evidence from 36 case-control studies.
BACKGROUND: Glutathione S-transferase M1 (GSTM1) is thought to be involved in detoxifying several carcinogens and may play a vital role in tumorigenesis. Numerous studies have evaluated the association between GSTM1 null/present polymorphism and risk of prostate cancer (PCa). However, the results re...
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doaj-279e4fcbb2c74d98b2468fab158f51cc2020-11-25T00:12:15ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01710e4698210.1371/journal.pone.0046982Association of GSTM1 null allele with prostate cancer risk: evidence from 36 case-control studies.Bingbing WeiZhuoqun XuYou ZhouJun RuanHuan ChengBo XiMing ZhuKe JinDeqi ZhouQiang HuQiang WangZhirong WangZhiqiang YanFeng XuanXing HuangJian ZhangHongyi ZhouBACKGROUND: Glutathione S-transferase M1 (GSTM1) is thought to be involved in detoxifying several carcinogens and may play a vital role in tumorigenesis. Numerous studies have evaluated the association between GSTM1 null/present polymorphism and risk of prostate cancer (PCa). However, the results remain inconsistent. To derive a more precise estimation, we performed a meta-analysis. METHODOLOGY/PRINCIPAL FINDINGS: A comprehensive search was conducted to identify all eligible case-control studies. We used odds ratios (ORs) with 95% confidence intervals (CIs) to assess the strength of the association. The overall association was significant (OR = 1.28, 95% CI: 1.11-1.48, P = 0.001). Moreover, subgroup analyses showed GSTM1 null genotype significantly associated with PCa risk among Asians (OR = 1.35, 95% CI: 1.03-1.78, P = 0.03) but not among Caucasians (OR = 1.12, 95% CI: 0.96-1.31, P = 0.16). In addition, we did not find that smoking modified the genotype effect on the risk of PCa. CONCLUSIONS/SIGNIFICANCE: The present meta-analysis suggested that GSTM1 null allele was a low-penetrant risk factor for PCa among Asians.http://europepmc.org/articles/PMC3468624?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Bingbing Wei Zhuoqun Xu You Zhou Jun Ruan Huan Cheng Bo Xi Ming Zhu Ke Jin Deqi Zhou Qiang Hu Qiang Wang Zhirong Wang Zhiqiang Yan Feng Xuan Xing Huang Jian Zhang Hongyi Zhou |
spellingShingle |
Bingbing Wei Zhuoqun Xu You Zhou Jun Ruan Huan Cheng Bo Xi Ming Zhu Ke Jin Deqi Zhou Qiang Hu Qiang Wang Zhirong Wang Zhiqiang Yan Feng Xuan Xing Huang Jian Zhang Hongyi Zhou Association of GSTM1 null allele with prostate cancer risk: evidence from 36 case-control studies. PLoS ONE |
author_facet |
Bingbing Wei Zhuoqun Xu You Zhou Jun Ruan Huan Cheng Bo Xi Ming Zhu Ke Jin Deqi Zhou Qiang Hu Qiang Wang Zhirong Wang Zhiqiang Yan Feng Xuan Xing Huang Jian Zhang Hongyi Zhou |
author_sort |
Bingbing Wei |
title |
Association of GSTM1 null allele with prostate cancer risk: evidence from 36 case-control studies. |
title_short |
Association of GSTM1 null allele with prostate cancer risk: evidence from 36 case-control studies. |
title_full |
Association of GSTM1 null allele with prostate cancer risk: evidence from 36 case-control studies. |
title_fullStr |
Association of GSTM1 null allele with prostate cancer risk: evidence from 36 case-control studies. |
title_full_unstemmed |
Association of GSTM1 null allele with prostate cancer risk: evidence from 36 case-control studies. |
title_sort |
association of gstm1 null allele with prostate cancer risk: evidence from 36 case-control studies. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2012-01-01 |
description |
BACKGROUND: Glutathione S-transferase M1 (GSTM1) is thought to be involved in detoxifying several carcinogens and may play a vital role in tumorigenesis. Numerous studies have evaluated the association between GSTM1 null/present polymorphism and risk of prostate cancer (PCa). However, the results remain inconsistent. To derive a more precise estimation, we performed a meta-analysis. METHODOLOGY/PRINCIPAL FINDINGS: A comprehensive search was conducted to identify all eligible case-control studies. We used odds ratios (ORs) with 95% confidence intervals (CIs) to assess the strength of the association. The overall association was significant (OR = 1.28, 95% CI: 1.11-1.48, P = 0.001). Moreover, subgroup analyses showed GSTM1 null genotype significantly associated with PCa risk among Asians (OR = 1.35, 95% CI: 1.03-1.78, P = 0.03) but not among Caucasians (OR = 1.12, 95% CI: 0.96-1.31, P = 0.16). In addition, we did not find that smoking modified the genotype effect on the risk of PCa. CONCLUSIONS/SIGNIFICANCE: The present meta-analysis suggested that GSTM1 null allele was a low-penetrant risk factor for PCa among Asians. |
url |
http://europepmc.org/articles/PMC3468624?pdf=render |
work_keys_str_mv |
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