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XPD Asp312Asn and Lys751Gln polymorphisms and breast cancer susceptibility: A meta-analysis
The association between xeroderma pigmentosum complementation group D (XPD) Asp312Asn and Lys751Gln gene polymorphisms and breast cancer risk has been widely reported, but the results were inconsistent. In order to derive a more precise estimation of the relationship, a meta-analysis was performed....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3967070/ https://www.ncbi.nlm.nih.gov/pubmed/24101192 http://dx.doi.org/10.1007/s13277-013-1256-3 |
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author | Yan, Yulan Liang, Hongjie Light, Morning Li, Taijie Deng, Yan Li, Meng Li, Shan Qin, Xue |
author_facet | Yan, Yulan Liang, Hongjie Light, Morning Li, Taijie Deng, Yan Li, Meng Li, Shan Qin, Xue |
author_sort | Yan, Yulan |
collection | PubMed |
description | The association between xeroderma pigmentosum complementation group D (XPD) Asp312Asn and Lys751Gln gene polymorphisms and breast cancer risk has been widely reported, but the results were inconsistent. In order to derive a more precise estimation of the relationship, a meta-analysis was performed. A comprehensive search strategy was conducted towards the electronic databases including Medline, PubMed, Web of Science, Embase, and Chinese Biomedical Literature Database (Chinese). The association between the XPD polymorphism and breast cancer risk was conducted by odds ratios (ORs) and 95 % confidence intervals (95 % CIs). A total of 22 studies with 18,136 cases and 18,351 controls were included in our meta-analysis. Among these, 12 studies with 7,667 cases and 7,480 controls for Asp312Asn polymorphism and 20 studies with 10,469 cases and 10,871 controls for Lys751Gln polymorphism. With regard to Asp312Asn polymorphism, no significantly associated was found with breast cancer risk. However, significant association was found between Lys751Gln polymorphism and breast cancer risk under all genetic models in overall populations (C vs. A—OR = 1.10, 95 % CI = 1.04–1.17, P = 0.002; CC vs. AA—OR = 1.17, 95 % CI = 1.06–1.30, P = 0.003; AC vs. AA—OR = 1.06, 95 % CI = 1.01–1.12, P = 0.032; CC vs. AC/AA—OR = 1.17, 95 % CI = 1.04–1.32, P = 0.009; CC/AC vs. AA—OR = 1.07, 95 % CI = 1.02–1.12, P = 0.005). In subgroup analysis base on ethnicity, significance was found in Caucasians and mix. The results suggest that XPD Asp312Asn polymorphism was not associated with breast cancer. The XPD Lys751Gln polymorphism significantly increased breast cancer risk, especially for Caucasian and mix. |
format | Online Article Text |
id | pubmed-3967070 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-39670702014-03-27 XPD Asp312Asn and Lys751Gln polymorphisms and breast cancer susceptibility: A meta-analysis Yan, Yulan Liang, Hongjie Light, Morning Li, Taijie Deng, Yan Li, Meng Li, Shan Qin, Xue Tumour Biol Research Article The association between xeroderma pigmentosum complementation group D (XPD) Asp312Asn and Lys751Gln gene polymorphisms and breast cancer risk has been widely reported, but the results were inconsistent. In order to derive a more precise estimation of the relationship, a meta-analysis was performed. A comprehensive search strategy was conducted towards the electronic databases including Medline, PubMed, Web of Science, Embase, and Chinese Biomedical Literature Database (Chinese). The association between the XPD polymorphism and breast cancer risk was conducted by odds ratios (ORs) and 95 % confidence intervals (95 % CIs). A total of 22 studies with 18,136 cases and 18,351 controls were included in our meta-analysis. Among these, 12 studies with 7,667 cases and 7,480 controls for Asp312Asn polymorphism and 20 studies with 10,469 cases and 10,871 controls for Lys751Gln polymorphism. With regard to Asp312Asn polymorphism, no significantly associated was found with breast cancer risk. However, significant association was found between Lys751Gln polymorphism and breast cancer risk under all genetic models in overall populations (C vs. A—OR = 1.10, 95 % CI = 1.04–1.17, P = 0.002; CC vs. AA—OR = 1.17, 95 % CI = 1.06–1.30, P = 0.003; AC vs. AA—OR = 1.06, 95 % CI = 1.01–1.12, P = 0.032; CC vs. AC/AA—OR = 1.17, 95 % CI = 1.04–1.32, P = 0.009; CC/AC vs. AA—OR = 1.07, 95 % CI = 1.02–1.12, P = 0.005). In subgroup analysis base on ethnicity, significance was found in Caucasians and mix. The results suggest that XPD Asp312Asn polymorphism was not associated with breast cancer. The XPD Lys751Gln polymorphism significantly increased breast cancer risk, especially for Caucasian and mix. Springer Netherlands 2013-10-08 /pmc/articles/PMC3967070/ /pubmed/24101192 http://dx.doi.org/10.1007/s13277-013-1256-3 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by-nc/2.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Research Article Yan, Yulan Liang, Hongjie Light, Morning Li, Taijie Deng, Yan Li, Meng Li, Shan Qin, Xue XPD Asp312Asn and Lys751Gln polymorphisms and breast cancer susceptibility: A meta-analysis |
title | XPD Asp312Asn and Lys751Gln polymorphisms and breast cancer susceptibility: A meta-analysis |
title_full | XPD Asp312Asn and Lys751Gln polymorphisms and breast cancer susceptibility: A meta-analysis |
title_fullStr | XPD Asp312Asn and Lys751Gln polymorphisms and breast cancer susceptibility: A meta-analysis |
title_full_unstemmed | XPD Asp312Asn and Lys751Gln polymorphisms and breast cancer susceptibility: A meta-analysis |
title_short | XPD Asp312Asn and Lys751Gln polymorphisms and breast cancer susceptibility: A meta-analysis |
title_sort | xpd asp312asn and lys751gln polymorphisms and breast cancer susceptibility: a meta-analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3967070/ https://www.ncbi.nlm.nih.gov/pubmed/24101192 http://dx.doi.org/10.1007/s13277-013-1256-3 |
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