GSTP1 Ile105Val polymorphism and prostate cancer risk: evidence from a meta-analysis.

BACKGROUND: Glutathione S-transferase P1 (GSTP1) is thought to be involved in the detoxification of reactive carcinogen metabolites. Numerous epidemiological studies have evaluated the association of GSTP1 Ile105Val polymorphism with the risk of prostate cancer. However, the results remain inconclus...

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Main Authors: Bingbing Wei, You Zhou, Zhuoqun Xu, Jun Ruan, Huan Cheng, Ming Zhu, Qiang Hu, Ke Jin, Zhiqiang Yan, Deqi Zhou, Feng Xuan, Hongyi Zhou, Zhirong Wang, Xing Huang, Qiang Wang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3747220?pdf=render
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author Bingbing Wei
You Zhou
Zhuoqun Xu
Jun Ruan
Huan Cheng
Ming Zhu
Qiang Hu
Ke Jin
Zhiqiang Yan
Deqi Zhou
Feng Xuan
Hongyi Zhou
Zhirong Wang
Xing Huang
Qiang Wang
author_facet Bingbing Wei
You Zhou
Zhuoqun Xu
Jun Ruan
Huan Cheng
Ming Zhu
Qiang Hu
Ke Jin
Zhiqiang Yan
Deqi Zhou
Feng Xuan
Hongyi Zhou
Zhirong Wang
Xing Huang
Qiang Wang
author_sort Bingbing Wei
collection DOAJ
description BACKGROUND: Glutathione S-transferase P1 (GSTP1) is thought to be involved in the detoxification of reactive carcinogen metabolites. Numerous epidemiological studies have evaluated the association of GSTP1 Ile105Val polymorphism with the risk of prostate cancer. However, the results remain inconclusive. To derive a more precise estimation, a meta-analysis was performed. METHODOLOGY/PRINCIPAL FINDINGS: A comprehensive search was conducted to identify the eligible studies. We used odds ratios (ORs) with 95% confidence intervals (CIs) to assess the strength of the relationship. The overall association was not significant (Val/Val vs. Ile/Ile OR = 1.06, 95% CI = 0.90-1.25, P = 0.50; Val/Val vs. Val/Ile+Ile/Ile: OR = 1.07, 95% CI = 0.91-1.25, P = 0.44). In subgroup analyses by ethnicity and prostate cancer grade, the similar results were observed. However, in stratified analysis by clinical stage, we found a significant association with low-stage prostate cancer (Val/Val vs. Ile/Ile: OR = 2.70, 95% CI = 1.73-4.22, P<0.001; Val/Val vs. Val/Ile+Ile/Ile: OR = 2.14, 95% CI = 1.38-3.33, P = 0.001). Moreover, there was no statistically significant evidence of multiplicative interactions neither between the GSTP1 Ile105Val polymorphism and GSTM1, nor between smoking status and GSTP1 on prostate cancer risk. CONCLUSIONS: This meta-analysis showed that GSTP1 Ile105Val polymorphism might not be significantly associated with overall prostate cancer risk. Further stratified analyses showed a significant association with low-stage prostate cancer.
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spelling doaj.art-a4bf7d0480db4e63b3e054d077e581142022-12-21T17:17:42ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0188e7164010.1371/journal.pone.0071640GSTP1 Ile105Val polymorphism and prostate cancer risk: evidence from a meta-analysis.Bingbing WeiYou ZhouZhuoqun XuJun RuanHuan ChengMing ZhuQiang HuKe JinZhiqiang YanDeqi ZhouFeng XuanHongyi ZhouZhirong WangXing HuangQiang WangBACKGROUND: Glutathione S-transferase P1 (GSTP1) is thought to be involved in the detoxification of reactive carcinogen metabolites. Numerous epidemiological studies have evaluated the association of GSTP1 Ile105Val polymorphism with the risk of prostate cancer. However, the results remain inconclusive. To derive a more precise estimation, a meta-analysis was performed. METHODOLOGY/PRINCIPAL FINDINGS: A comprehensive search was conducted to identify the eligible studies. We used odds ratios (ORs) with 95% confidence intervals (CIs) to assess the strength of the relationship. The overall association was not significant (Val/Val vs. Ile/Ile OR = 1.06, 95% CI = 0.90-1.25, P = 0.50; Val/Val vs. Val/Ile+Ile/Ile: OR = 1.07, 95% CI = 0.91-1.25, P = 0.44). In subgroup analyses by ethnicity and prostate cancer grade, the similar results were observed. However, in stratified analysis by clinical stage, we found a significant association with low-stage prostate cancer (Val/Val vs. Ile/Ile: OR = 2.70, 95% CI = 1.73-4.22, P<0.001; Val/Val vs. Val/Ile+Ile/Ile: OR = 2.14, 95% CI = 1.38-3.33, P = 0.001). Moreover, there was no statistically significant evidence of multiplicative interactions neither between the GSTP1 Ile105Val polymorphism and GSTM1, nor between smoking status and GSTP1 on prostate cancer risk. CONCLUSIONS: This meta-analysis showed that GSTP1 Ile105Val polymorphism might not be significantly associated with overall prostate cancer risk. Further stratified analyses showed a significant association with low-stage prostate cancer.http://europepmc.org/articles/PMC3747220?pdf=render
spellingShingle Bingbing Wei
You Zhou
Zhuoqun Xu
Jun Ruan
Huan Cheng
Ming Zhu
Qiang Hu
Ke Jin
Zhiqiang Yan
Deqi Zhou
Feng Xuan
Hongyi Zhou
Zhirong Wang
Xing Huang
Qiang Wang
GSTP1 Ile105Val polymorphism and prostate cancer risk: evidence from a meta-analysis.
PLoS ONE
title GSTP1 Ile105Val polymorphism and prostate cancer risk: evidence from a meta-analysis.
title_full GSTP1 Ile105Val polymorphism and prostate cancer risk: evidence from a meta-analysis.
title_fullStr GSTP1 Ile105Val polymorphism and prostate cancer risk: evidence from a meta-analysis.
title_full_unstemmed GSTP1 Ile105Val polymorphism and prostate cancer risk: evidence from a meta-analysis.
title_short GSTP1 Ile105Val polymorphism and prostate cancer risk: evidence from a meta-analysis.
title_sort gstp1 ile105val polymorphism and prostate cancer risk evidence from a meta analysis
url http://europepmc.org/articles/PMC3747220?pdf=render
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