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Erschienen in: Breast Cancer Research and Treatment 3/2012

01.12.2012 | Epidemiology

The SLC4A7 variant rs4973768 is associated with breast cancer risk: evidence from a case–control study and a meta-analysis

verfasst von: Wei Chen, Rong Zhong, Jie Ming, Li Zou, Beibei Zhu, Xuzai Lu, Juntao Ke, Yu Zhang, Li Liu, Xiaoping Miao, Tao Huang

Erschienen in: Breast Cancer Research and Treatment | Ausgabe 3/2012

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Abstract

Recent genome-wide association study has identified a genetic variant rs4973768, located in 3′-UTR of solute carrier family 4, sodium bicarbonate cotransporter, member 7 (SLC4A7), was associated with increased risk of breast cancer (BC). However, several following replication studies cannot yield consistent results. We thus conducted a hospital-based case–control study including 485 patients and 514 controls, combined a meta-analysis including 108,632 cases and 135,818 controls to explore the relationship between this variant and BC risk. Our case–control study showed that rs4973768 was significantly associated with increased BC risk with the odds ratio (OR) of 1.29 (95 % confidence interval [CI]: 1.04–1.60) under the allelic model. In addition, the meta-analysis also indicated that the variant slightly increased the risk of BC with the pooled OR of the per-allele effect being 1.08 (95 % CI: 1.04–1.11) although with significant heterogeneity between studies. Stratified analyses showed that ethnicity, sample size, and study design may explain part of the heterogeneity. Moreover, the bioinformatics analysis suggested that this variant may influence the transcriptional capacity of SLC4A7. In summary, our results showed that the SLC4A7 variant, rs4973768, is associated with risk of BC although the underlying biologic mechanism warrants further studies.
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Metadaten
Titel
The SLC4A7 variant rs4973768 is associated with breast cancer risk: evidence from a case–control study and a meta-analysis
verfasst von
Wei Chen
Rong Zhong
Jie Ming
Li Zou
Beibei Zhu
Xuzai Lu
Juntao Ke
Yu Zhang
Li Liu
Xiaoping Miao
Tao Huang
Publikationsdatum
01.12.2012
Verlag
Springer US
Erschienen in
Breast Cancer Research and Treatment / Ausgabe 3/2012
Print ISSN: 0167-6806
Elektronische ISSN: 1573-7217
DOI
https://doi.org/10.1007/s10549-012-2309-9

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