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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...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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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 |
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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 |
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