Lack of an association between two BER gene polymorphisms and breast cancer risk: a meta-analysis.

The base excision repair (BER) pathway removes DNA damage caused by ionizing radiation, reactive oxidative species and methylating agents. ADPRT and APE1 are two important genes in the BER pathway. Several studies have evaluated the association between polymorphisms in the two BER genes (ADPRT Val76...

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Main Authors: Bian Wu, Hong-Li Liu, Sheng Zhang, Xiao-Rong Dong, Gang Wu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3522727?pdf=render
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spelling doaj-4637e2aa206f404ba038d6cb5dcbd09b2020-11-24T20:50:08ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01712e5085710.1371/journal.pone.0050857Lack of an association between two BER gene polymorphisms and breast cancer risk: a meta-analysis.Bian WuHong-Li LiuSheng ZhangXiao-Rong DongGang WuThe base excision repair (BER) pathway removes DNA damage caused by ionizing radiation, reactive oxidative species and methylating agents. ADPRT and APE1 are two important genes in the BER pathway. Several studies have evaluated the association between polymorphisms in the two BER genes (ADPRT Val762Ala and APE1 Asp148Glu) and breast cancer risk. However, the results are inconsistent.In this study, we conducted a meta-analysis to derive a more precise estimation. A total of 8 studies were included in the meta-analysis (6 studies with 2,521 cases and 2,652 controls for ADPRT Val762Ala polymorphism and 5 studies with 2,539 cases and 2,572 controls for APE1 Asp148Glu polymorphism). For ADPRT Val762Ala polymorphism, no obvious associations were found for all genetic models (Val/Ala vs. Val/Val: OR = 0.960, 95% CI = 0.845-1.090; Ala/Ala vs. Val/Val: OR = 0.897, 95% CI = 0.683-1.178; dominant model: OR = 0.953, 95% CI = 0.843-1.077; and recessive model: OR = 1.084, 95% CI = 0.838-1.403). For APE1 Asp148Glu polymorphism, also no obvious associations were found for all genetic models (Asp/Glu vs. Asp/Asp: OR = 0.947, 95% CI = 0.829-1.082; Glu/Glu vs. Asp/Asp: OR = 0.958, 95% CI = 0.813-1.129; dominant model: OR = 0.946, 95% CI = 0.835-1.072; and recessive model: OR = 1.004, 95% CI = 0.873-1.155). In the subgroup analysis by ethnicity or study design, still no obvious associations were found.This meta-analysis indicates that ADPRT Val762Ala and APE1 Asp148Glu polymorphisms are not associated with increased breast cancer risk.http://europepmc.org/articles/PMC3522727?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Bian Wu
Hong-Li Liu
Sheng Zhang
Xiao-Rong Dong
Gang Wu
spellingShingle Bian Wu
Hong-Li Liu
Sheng Zhang
Xiao-Rong Dong
Gang Wu
Lack of an association between two BER gene polymorphisms and breast cancer risk: a meta-analysis.
PLoS ONE
author_facet Bian Wu
Hong-Li Liu
Sheng Zhang
Xiao-Rong Dong
Gang Wu
author_sort Bian Wu
title Lack of an association between two BER gene polymorphisms and breast cancer risk: a meta-analysis.
title_short Lack of an association between two BER gene polymorphisms and breast cancer risk: a meta-analysis.
title_full Lack of an association between two BER gene polymorphisms and breast cancer risk: a meta-analysis.
title_fullStr Lack of an association between two BER gene polymorphisms and breast cancer risk: a meta-analysis.
title_full_unstemmed Lack of an association between two BER gene polymorphisms and breast cancer risk: a meta-analysis.
title_sort lack of an association between two ber gene polymorphisms and breast cancer risk: a meta-analysis.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description The base excision repair (BER) pathway removes DNA damage caused by ionizing radiation, reactive oxidative species and methylating agents. ADPRT and APE1 are two important genes in the BER pathway. Several studies have evaluated the association between polymorphisms in the two BER genes (ADPRT Val762Ala and APE1 Asp148Glu) and breast cancer risk. However, the results are inconsistent.In this study, we conducted a meta-analysis to derive a more precise estimation. A total of 8 studies were included in the meta-analysis (6 studies with 2,521 cases and 2,652 controls for ADPRT Val762Ala polymorphism and 5 studies with 2,539 cases and 2,572 controls for APE1 Asp148Glu polymorphism). For ADPRT Val762Ala polymorphism, no obvious associations were found for all genetic models (Val/Ala vs. Val/Val: OR = 0.960, 95% CI = 0.845-1.090; Ala/Ala vs. Val/Val: OR = 0.897, 95% CI = 0.683-1.178; dominant model: OR = 0.953, 95% CI = 0.843-1.077; and recessive model: OR = 1.084, 95% CI = 0.838-1.403). For APE1 Asp148Glu polymorphism, also no obvious associations were found for all genetic models (Asp/Glu vs. Asp/Asp: OR = 0.947, 95% CI = 0.829-1.082; Glu/Glu vs. Asp/Asp: OR = 0.958, 95% CI = 0.813-1.129; dominant model: OR = 0.946, 95% CI = 0.835-1.072; and recessive model: OR = 1.004, 95% CI = 0.873-1.155). In the subgroup analysis by ethnicity or study design, still no obvious associations were found.This meta-analysis indicates that ADPRT Val762Ala and APE1 Asp148Glu polymorphisms are not associated with increased breast cancer risk.
url http://europepmc.org/articles/PMC3522727?pdf=render
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