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Erschienen in: Breast Cancer Research and Treatment 3/2011

01.02.2011 | Epidemiology

RAD51 135G/C polymorphism and breast cancer risk: a meta-analysis from 21 studies

verfasst von: Lin-Bo Gao, Xin-Min Pan, Li-Juan Li, Wei-Bo Liang, Yi Zhu, Lu-Shun Zhang, Yong-Gang Wei, Ming Tang, Lin Zhang

Erschienen in: Breast Cancer Research and Treatment | Ausgabe 3/2011

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Abstract

Growing evidence suggests that RAD51 plays a pivotal role in the repair of DNA double-strand breaks and the maintenance of genomic stability. A single nucleotide polymorphism, 135G/C, has been identified in the 5′ untranslated region of the RAD51 gene and has been shown to influence gene transcription activity. Previous studies yielded conflicting results as to the association of 135G/C polymorphism with breast cancer. We aimed to assess the effect of 135G/C of RAD51 on breast cancer susceptibility with the use of a meta-analysis. We performed a meta-analysis of 21 published case–control studies up to April 2010. We found that the CC genotype was associated with a significantly increased risk of breast cancer when compared with the GG, CG, and CG/GG genotypes. Subgroup analyses showed that individuals carrying the CC genotype were associated with an elevated tumor risk in European populations and in sporadic breast cancer. After stratified analyses according to manuscript quality, the CC genotype was associated with a significantly increased risk of breast cancer compared with the CG genotype in studies of both higher and lower quality. However, significantly elevated risk was found in studies of higher quality, but not in studies of lower quality when homozygote and a recessive comparison model were tested. This meta-analysis indicates that RAD51 135G/C polymorphism may be identified as a susceptibility locus for breast cancer.
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Metadaten
Titel
RAD51 135G/C polymorphism and breast cancer risk: a meta-analysis from 21 studies
verfasst von
Lin-Bo Gao
Xin-Min Pan
Li-Juan Li
Wei-Bo Liang
Yi Zhu
Lu-Shun Zhang
Yong-Gang Wei
Ming Tang
Lin Zhang
Publikationsdatum
01.02.2011
Verlag
Springer US
Erschienen in
Breast Cancer Research and Treatment / Ausgabe 3/2011
Print ISSN: 0167-6806
Elektronische ISSN: 1573-7217
DOI
https://doi.org/10.1007/s10549-010-0995-8

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