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Association Between rs2981582 Polymorphism in the FGFR2 Gene and the Risk of Breast Cancer in Mexican Women.

Authors :
Murillo-Zamora, Efrén
Moreno-Macías, Hortensia
Ziv, Elad
Romieu, Isabelle
Lazcano-Ponce, Eduardo
Ángeles-Llerenas, Angélica
Pérez-Rodríguez, Edelmiro
Vidal-Millán, Silvia
Fejerman, Laura
Torres-Mejía, Gabriela
Source :
Archives of Medical Research. Aug2013, Vol. 44 Issue 6, p459-466. 8p.
Publication Year :
2013

Abstract

Background and Aims: The rs2981582 single nucleotide polymorphism in the fibroblast growth factor receptor 2 gene has been consistently associated with an increased risk of breast cancer. We evaluated the effect of rs2981582 polymorphism in the FGFR2 gene on the risk of breast cancer and its interaction with non-genetic risk factors. Methods: A population-based case-control study was conducted in Mexico. Data from 687 cases and 907 controls were analyzed. Results: The T allele of the rs2981582 polymorphism was associated with an increased risk of breast cancer (ORper allele = 1.24, 95% CI 1.06–1.46). There was also an interaction between this polymorphism and alcohol consumption (p = 0.043). The effect of alcohol consumption on the risk of breast cancer varied according to the allelic variants of the rs2981582 polymorphism in the FGFR2 gene: OR = 3.97 (95% CI 2.10–7.49), OR = 2.01 (95% CI 1.23–3.29) and OR = 1.21 (95% CI 0.48–3.05) for genotypes CC, CT and TT, respectively. Conclusions: This is the first study exploring the association between rs2981582 polymorphism in the FGFR2 gene and breast cancer risk in Mexican women. The interaction found may be of great public health interest because alcohol consumption is a modifiable breast cancer risk factor. Therefore, replication of this finding is of foremost importance. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
01884409
Volume :
44
Issue :
6
Database :
Academic Search Index
Journal :
Archives of Medical Research
Publication Type :
Academic Journal
Accession number :
90627530
Full Text :
https://doi.org/10.1016/j.arcmed.2013.08.006