Cargando…

The association between ATM D1853N polymorphism and breast cancer susceptibility: a meta-analysis

BACKGROUND: Emerging evidence suggests that ataxia telangiectasia-mutated (ATM) is involved in numerous damage repair signaling pathways and cell-cycle checkpoints. Heterozygous carriers of ATM-mutations have an increased risk for the development of breast cancer. The purpose of this study is to eva...

Descripción completa

Detalles Bibliográficos
Autores principales: Gao, Lin-Bo, Pan, Xin-Min, Sun, Hong, Wang, Xia, Rao, Li, Li, Li-Juan, Liang, Wei-Bo, Lv, Mei-Li, Yang, Wen-Zhong, Zhang, Lin
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936337/
https://www.ncbi.nlm.nih.gov/pubmed/20799949
http://dx.doi.org/10.1186/1756-9966-29-117
_version_ 1782186471701086208
author Gao, Lin-Bo
Pan, Xin-Min
Sun, Hong
Wang, Xia
Rao, Li
Li, Li-Juan
Liang, Wei-Bo
Lv, Mei-Li
Yang, Wen-Zhong
Zhang, Lin
author_facet Gao, Lin-Bo
Pan, Xin-Min
Sun, Hong
Wang, Xia
Rao, Li
Li, Li-Juan
Liang, Wei-Bo
Lv, Mei-Li
Yang, Wen-Zhong
Zhang, Lin
author_sort Gao, Lin-Bo
collection PubMed
description BACKGROUND: Emerging evidence suggests that ataxia telangiectasia-mutated (ATM) is involved in numerous damage repair signaling pathways and cell-cycle checkpoints. Heterozygous carriers of ATM-mutations have an increased risk for the development of breast cancer. The purpose of this study is to evaluate the association between ATM exon39 5557G > A (D1853N, rs1801516) polymorphism and breast cancer susceptibility with the use of a meta-analysis. METHODS: By searching PubMed and Embase databases, a total of 9 epidemiological studies with 4,191 cases and 3,780 controls were identified. Crude odds ratios (ORs) and their corresponding 95% confidence intervals (CIs) for ATM D1853N polymorphism and breast cancer risk were calculated using fixed- or random-effects model based on the degree of heterogeneity among studies. RESULTS: No significant association between the ATM D1853N polymorphism and breast cancer risk was observed in overall analysis (GA versus GG: OR = 1.18; 95% CI, 0.90-1.53; AA versus GG: OR = 0.77; 95% CI, 0.58-1.03; dominant model: OR = 1.16; 95% CI, 0.89-1.51; and recessive model: OR = 0.78; 95% CI, 0.59-1.04, respectively). CONCLUSION: Our results indicate that ATM D1853N polymorphism is not a risk factor for developing breast cancer.
format Text
id pubmed-2936337
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-29363372010-09-10 The association between ATM D1853N polymorphism and breast cancer susceptibility: a meta-analysis Gao, Lin-Bo Pan, Xin-Min Sun, Hong Wang, Xia Rao, Li Li, Li-Juan Liang, Wei-Bo Lv, Mei-Li Yang, Wen-Zhong Zhang, Lin J Exp Clin Cancer Res Research BACKGROUND: Emerging evidence suggests that ataxia telangiectasia-mutated (ATM) is involved in numerous damage repair signaling pathways and cell-cycle checkpoints. Heterozygous carriers of ATM-mutations have an increased risk for the development of breast cancer. The purpose of this study is to evaluate the association between ATM exon39 5557G > A (D1853N, rs1801516) polymorphism and breast cancer susceptibility with the use of a meta-analysis. METHODS: By searching PubMed and Embase databases, a total of 9 epidemiological studies with 4,191 cases and 3,780 controls were identified. Crude odds ratios (ORs) and their corresponding 95% confidence intervals (CIs) for ATM D1853N polymorphism and breast cancer risk were calculated using fixed- or random-effects model based on the degree of heterogeneity among studies. RESULTS: No significant association between the ATM D1853N polymorphism and breast cancer risk was observed in overall analysis (GA versus GG: OR = 1.18; 95% CI, 0.90-1.53; AA versus GG: OR = 0.77; 95% CI, 0.58-1.03; dominant model: OR = 1.16; 95% CI, 0.89-1.51; and recessive model: OR = 0.78; 95% CI, 0.59-1.04, respectively). CONCLUSION: Our results indicate that ATM D1853N polymorphism is not a risk factor for developing breast cancer. BioMed Central 2010-08-27 /pmc/articles/PMC2936337/ /pubmed/20799949 http://dx.doi.org/10.1186/1756-9966-29-117 Text en Copyright ©2010 Gao et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Gao, Lin-Bo
Pan, Xin-Min
Sun, Hong
Wang, Xia
Rao, Li
Li, Li-Juan
Liang, Wei-Bo
Lv, Mei-Li
Yang, Wen-Zhong
Zhang, Lin
The association between ATM D1853N polymorphism and breast cancer susceptibility: a meta-analysis
title The association between ATM D1853N polymorphism and breast cancer susceptibility: a meta-analysis
title_full The association between ATM D1853N polymorphism and breast cancer susceptibility: a meta-analysis
title_fullStr The association between ATM D1853N polymorphism and breast cancer susceptibility: a meta-analysis
title_full_unstemmed The association between ATM D1853N polymorphism and breast cancer susceptibility: a meta-analysis
title_short The association between ATM D1853N polymorphism and breast cancer susceptibility: a meta-analysis
title_sort association between atm d1853n polymorphism and breast cancer susceptibility: a meta-analysis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936337/
https://www.ncbi.nlm.nih.gov/pubmed/20799949
http://dx.doi.org/10.1186/1756-9966-29-117
work_keys_str_mv AT gaolinbo theassociationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis
AT panxinmin theassociationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis
AT sunhong theassociationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis
AT wangxia theassociationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis
AT raoli theassociationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis
AT lilijuan theassociationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis
AT liangweibo theassociationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis
AT lvmeili theassociationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis
AT yangwenzhong theassociationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis
AT zhanglin theassociationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis
AT gaolinbo associationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis
AT panxinmin associationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis
AT sunhong associationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis
AT wangxia associationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis
AT raoli associationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis
AT lilijuan associationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis
AT liangweibo associationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis
AT lvmeili associationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis
AT yangwenzhong associationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis
AT zhanglin associationbetweenatmd1853npolymorphismandbreastcancersusceptibilityametaanalysis