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Association between ERα gene Pvu II polymorphism and breast cancer susceptibility: A meta-analysis

BACKGROUND: Estrogen has played an important role in the development of breast cancer. ER-α PvuII gene polymorphism is in close association with the occurrence risk of breast cancer, but no consensus has been achieved currently. METHODS: PubMed, Embase, China National Knowledge Infrastructure (CNKI)...

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Autores principales: Zhang, Zhen-lian, Zhang, Cui-zhen, Li, Yan, Zhao, Zhen-hui, Yang, Shun-e
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944501/
https://www.ncbi.nlm.nih.gov/pubmed/29702977
http://dx.doi.org/10.1097/MD.0000000000010317
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author Zhang, Zhen-lian
Zhang, Cui-zhen
Li, Yan
Zhao, Zhen-hui
Yang, Shun-e
author_facet Zhang, Zhen-lian
Zhang, Cui-zhen
Li, Yan
Zhao, Zhen-hui
Yang, Shun-e
author_sort Zhang, Zhen-lian
collection PubMed
description BACKGROUND: Estrogen has played an important role in the development of breast cancer. ER-α PvuII gene polymorphism is in close association with the occurrence risk of breast cancer, but no consensus has been achieved currently. METHODS: PubMed, Embase, China National Knowledge Infrastructure (CNKI) database, Wanfang database, and VIP database were retrieved to collect the case–control studies on association between ERα gene Pvu II polymorphism and breast cancer risk published before September 1, 2017. Newcastle–Ottawa Scale (NOS) was used to assess the quality of the literatures, Stata 14.0 software was applied for meta-analysis, and the pooled odds ratio (OR) and 95% confidence interval (95% CI) were calculated. The subgroup analysis was performed to assess the confounding factors, followed by assessment of publication bias and sensitivity analysis. RESULTS: A total of 26 studies were enrolled in the analysis based on inclusion criteria, which included 15,360 patients and 26,423 controls. The results demonstrated that ERα gene Pvu II polymorphism was in significant association with the decrease of breast cancer risk in 3 genetic models (C vs T, OR = 0.962, 95% CI = 0.933–0.992, P = .012; CC vs TT, OR = 0.911, 95% CI = 0.856–0.969, P = .003; CC vs TT/CT, OR = 0.923, 95% CI = 0.874–0.975, P = .004). Subgroup analysis was conducted on the basis of ethnicity and source of controls, whose results illustrated that ERα gene Pvu II polymorphism was in significant association with the decrease of breast cancer risk in Asians rather than in Caucasians (CC vs TT, OR = 0.862, 95% CI = 0.750–0.922, P = .038; CC vs TT/CT, OR = 0.851, 95% CI = 0.755–0.959, P = .008). In population-based subgroup rather than in hospital-based subgroup, ERα gene Pvu II polymorphism was in significant association with the decrease of breast cancer risk in the allele model, homozygous model, dominant model, and recessive model (C vs T, OR = 0.943, 95% CI = 0.911–0.977, P = .001; CC vs TT, OR = 0.878, 95% CI = 0.817–0.944, P = .000; CC/CT vs TT, OR = 0.936, 95% CI = 0.881–0.994, P = .031; CC vs TT/CT, OR = 0.902, 95% CI = 0.847–0.960, P = .001). CONCLUSION: ERα gene Pvu II polymorphism exerts an important function in the progression of breast cancer.
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spelling pubmed-59445012018-05-15 Association between ERα gene Pvu II polymorphism and breast cancer susceptibility: A meta-analysis Zhang, Zhen-lian Zhang, Cui-zhen Li, Yan Zhao, Zhen-hui Yang, Shun-e Medicine (Baltimore) Research Article BACKGROUND: Estrogen has played an important role in the development of breast cancer. ER-α PvuII gene polymorphism is in close association with the occurrence risk of breast cancer, but no consensus has been achieved currently. METHODS: PubMed, Embase, China National Knowledge Infrastructure (CNKI) database, Wanfang database, and VIP database were retrieved to collect the case–control studies on association between ERα gene Pvu II polymorphism and breast cancer risk published before September 1, 2017. Newcastle–Ottawa Scale (NOS) was used to assess the quality of the literatures, Stata 14.0 software was applied for meta-analysis, and the pooled odds ratio (OR) and 95% confidence interval (95% CI) were calculated. The subgroup analysis was performed to assess the confounding factors, followed by assessment of publication bias and sensitivity analysis. RESULTS: A total of 26 studies were enrolled in the analysis based on inclusion criteria, which included 15,360 patients and 26,423 controls. The results demonstrated that ERα gene Pvu II polymorphism was in significant association with the decrease of breast cancer risk in 3 genetic models (C vs T, OR = 0.962, 95% CI = 0.933–0.992, P = .012; CC vs TT, OR = 0.911, 95% CI = 0.856–0.969, P = .003; CC vs TT/CT, OR = 0.923, 95% CI = 0.874–0.975, P = .004). Subgroup analysis was conducted on the basis of ethnicity and source of controls, whose results illustrated that ERα gene Pvu II polymorphism was in significant association with the decrease of breast cancer risk in Asians rather than in Caucasians (CC vs TT, OR = 0.862, 95% CI = 0.750–0.922, P = .038; CC vs TT/CT, OR = 0.851, 95% CI = 0.755–0.959, P = .008). In population-based subgroup rather than in hospital-based subgroup, ERα gene Pvu II polymorphism was in significant association with the decrease of breast cancer risk in the allele model, homozygous model, dominant model, and recessive model (C vs T, OR = 0.943, 95% CI = 0.911–0.977, P = .001; CC vs TT, OR = 0.878, 95% CI = 0.817–0.944, P = .000; CC/CT vs TT, OR = 0.936, 95% CI = 0.881–0.994, P = .031; CC vs TT/CT, OR = 0.902, 95% CI = 0.847–0.960, P = .001). CONCLUSION: ERα gene Pvu II polymorphism exerts an important function in the progression of breast cancer. Wolters Kluwer Health 2018-04-27 /pmc/articles/PMC5944501/ /pubmed/29702977 http://dx.doi.org/10.1097/MD.0000000000010317 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Research Article
Zhang, Zhen-lian
Zhang, Cui-zhen
Li, Yan
Zhao, Zhen-hui
Yang, Shun-e
Association between ERα gene Pvu II polymorphism and breast cancer susceptibility: A meta-analysis
title Association between ERα gene Pvu II polymorphism and breast cancer susceptibility: A meta-analysis
title_full Association between ERα gene Pvu II polymorphism and breast cancer susceptibility: A meta-analysis
title_fullStr Association between ERα gene Pvu II polymorphism and breast cancer susceptibility: A meta-analysis
title_full_unstemmed Association between ERα gene Pvu II polymorphism and breast cancer susceptibility: A meta-analysis
title_short Association between ERα gene Pvu II polymorphism and breast cancer susceptibility: A meta-analysis
title_sort association between erα gene pvu ii polymorphism and breast cancer susceptibility: a meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944501/
https://www.ncbi.nlm.nih.gov/pubmed/29702977
http://dx.doi.org/10.1097/MD.0000000000010317
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