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ESR1 Gene Polymorphisms and Prostate Cancer Risk: A HuGE Review and Meta-Analysis

BACKGROUND: Many published data on the association between single nucleotide polymorphisms (SNPs) in the ESR1 gene and prostate cancer susceptibility are inconclusive. The aim of this Human Genome Epidemiology (HuGE) review and meta-analysis is to derive a more precise estimation of this relationshi...

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Autores principales: Wang, Yu-Mei, Liu, Zu-Wang, Guo, Jing-Bo, Wang, Xiao-Fang, Zhao, Xin-Xin, Zheng, Xuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3689664/
https://www.ncbi.nlm.nih.gov/pubmed/23805288
http://dx.doi.org/10.1371/journal.pone.0066999
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author Wang, Yu-Mei
Liu, Zu-Wang
Guo, Jing-Bo
Wang, Xiao-Fang
Zhao, Xin-Xin
Zheng, Xuan
author_facet Wang, Yu-Mei
Liu, Zu-Wang
Guo, Jing-Bo
Wang, Xiao-Fang
Zhao, Xin-Xin
Zheng, Xuan
author_sort Wang, Yu-Mei
collection PubMed
description BACKGROUND: Many published data on the association between single nucleotide polymorphisms (SNPs) in the ESR1 gene and prostate cancer susceptibility are inconclusive. The aim of this Human Genome Epidemiology (HuGE) review and meta-analysis is to derive a more precise estimation of this relationship. METHODS: A literature search of PubMed, Embase, Web of Science and Chinese Biomedical (CBM) databases was conducted from their inception through July 1st, 2012. Crude odds ratios (ORs) with 95% confidence intervals (CIs) were calculated to assess the strength of association. RESULTS: Twelve case-control studies were included with a total 2,165 prostate cancer cases and 3,361 healthy controls. When all the eligible studies were pooled into the meta-analysis, ESR1 PvuII (C>T) and XbaI (A>G) polymorphisms showed no association with the risk of prostate cancer. However, in the stratified analyses based on ethnicity and country, the results indicated that ESR1 PvuII (C>T) polymorphism was significantly associated with increased risk of prostate cancer among Asian populations, especially among Indian population; while ESR1 XbaI (A>G) polymorphism may significantly increase the risk of prostate cancer among American population. Furthermore, we also performed a pooled analysis for all eligible case-control studies to explore the role of codon 10 (T>C), codon 325 (C>G), codon 594 (G>A) and +261G>C polymorphisms in prostate cancer risk. Nevertheless, no significant associations between these polymorphisms and the risk of prostate cancer were observed. CONCLUSION: Results from the current meta-analysis indicate that ESR1 PvuII (C>T) polymorphism may be a risk factor for prostate cancer among Asian populations, especially among Indian population; while ESR1 XbaI (A>G) polymorphism may increase the risk of prostate cancer among American population.
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spelling pubmed-36896642013-06-26 ESR1 Gene Polymorphisms and Prostate Cancer Risk: A HuGE Review and Meta-Analysis Wang, Yu-Mei Liu, Zu-Wang Guo, Jing-Bo Wang, Xiao-Fang Zhao, Xin-Xin Zheng, Xuan PLoS One Research Article BACKGROUND: Many published data on the association between single nucleotide polymorphisms (SNPs) in the ESR1 gene and prostate cancer susceptibility are inconclusive. The aim of this Human Genome Epidemiology (HuGE) review and meta-analysis is to derive a more precise estimation of this relationship. METHODS: A literature search of PubMed, Embase, Web of Science and Chinese Biomedical (CBM) databases was conducted from their inception through July 1st, 2012. Crude odds ratios (ORs) with 95% confidence intervals (CIs) were calculated to assess the strength of association. RESULTS: Twelve case-control studies were included with a total 2,165 prostate cancer cases and 3,361 healthy controls. When all the eligible studies were pooled into the meta-analysis, ESR1 PvuII (C>T) and XbaI (A>G) polymorphisms showed no association with the risk of prostate cancer. However, in the stratified analyses based on ethnicity and country, the results indicated that ESR1 PvuII (C>T) polymorphism was significantly associated with increased risk of prostate cancer among Asian populations, especially among Indian population; while ESR1 XbaI (A>G) polymorphism may significantly increase the risk of prostate cancer among American population. Furthermore, we also performed a pooled analysis for all eligible case-control studies to explore the role of codon 10 (T>C), codon 325 (C>G), codon 594 (G>A) and +261G>C polymorphisms in prostate cancer risk. Nevertheless, no significant associations between these polymorphisms and the risk of prostate cancer were observed. CONCLUSION: Results from the current meta-analysis indicate that ESR1 PvuII (C>T) polymorphism may be a risk factor for prostate cancer among Asian populations, especially among Indian population; while ESR1 XbaI (A>G) polymorphism may increase the risk of prostate cancer among American population. Public Library of Science 2013-06-21 /pmc/articles/PMC3689664/ /pubmed/23805288 http://dx.doi.org/10.1371/journal.pone.0066999 Text en © 2013 Wang 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
Wang, Yu-Mei
Liu, Zu-Wang
Guo, Jing-Bo
Wang, Xiao-Fang
Zhao, Xin-Xin
Zheng, Xuan
ESR1 Gene Polymorphisms and Prostate Cancer Risk: A HuGE Review and Meta-Analysis
title ESR1 Gene Polymorphisms and Prostate Cancer Risk: A HuGE Review and Meta-Analysis
title_full ESR1 Gene Polymorphisms and Prostate Cancer Risk: A HuGE Review and Meta-Analysis
title_fullStr ESR1 Gene Polymorphisms and Prostate Cancer Risk: A HuGE Review and Meta-Analysis
title_full_unstemmed ESR1 Gene Polymorphisms and Prostate Cancer Risk: A HuGE Review and Meta-Analysis
title_short ESR1 Gene Polymorphisms and Prostate Cancer Risk: A HuGE Review and Meta-Analysis
title_sort esr1 gene polymorphisms and prostate cancer risk: a huge review and meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3689664/
https://www.ncbi.nlm.nih.gov/pubmed/23805288
http://dx.doi.org/10.1371/journal.pone.0066999
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