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Functional polymorphisms in the BRCA1 promoter influence transcription and are associated with decreased risk for breast cancer in Chinese women.
Functional polymorphisms in the BRCA1 promoter influence transcription and are associated with decreased risk for breast cancer in Chinese women.
- Source :
-
Journal of medical genetics [J Med Genet] 2009 Jan; Vol. 46 (1), pp. 32-9. Date of Electronic Publication: 2008 Sep 09. - Publication Year :
- 2009
-
Abstract
- Background: The BRCA1 gene is an important breast-cancer susceptibility gene. Promoter polymorphisms can alter the binding affinity of transcription factors, changing transcriptional activity and may affect susceptibility to disease.<br />Methods and Results: Using direct sequencing of the BRCA1 promoter region, we identified four polymorphisms c.-2804T-->C (rs799908:T-->C), c.-2265C-->T (rs11655505:C-->T), c.-2004A-->G (rs799906:A-->G) and c.-1896(ACA)(1)-->(ACA)(2) (rs8176071:(ACA)(1)-->(ACA)(2)) present in Hong Kong Chinese. Each polymorphism was studied independently and in combination by functional assays. Although all four variants significantly altered promoter activity, the c.-2265T allele had stronger binding than the C allele, and the most common mutant haplotype, which contains the c.-2265T allele, increased promoter activity by 70%. Risk association first tested in Hong Kong Chinese women with breast cancer and age-matched controls and replicated in a large population-based study of Shanghai Chinese, together totalling >3000 participants, showed that carriers of the c.-2265T allele had a reduced risk for breast cancer (combined odd ratio (OR) = 0.80, 95% CI 0.69 to 0.93; p = 0.003) which was more evident among women aged >or=45 years at first diagnosis of breast cancer and without a family history of breast cancer (combined OR = 0.75, 95% CI 0.61 to 0.91; p = 0.004). The most common haplotype containing the c.-2265T allele also showed significant risk association for women aged >or=45 years without a family history of breast cancer (OR = 0.64, 95% CI 0.46 to 0.89; p = 0.008).<br />Conclusion: This comprehensive study of BRCA1 promoter polymorphisms found four variants that altered promoter activity and with the most significant contribution from c.-2265C-->T, which could affect susceptibility to breast cancer in the Chinese population. Its significance in other populations remains to be investigated.
- Subjects :
- Asian People genetics
Binding Sites
Breast Neoplasms epidemiology
Case-Control Studies
China epidemiology
Cohort Studies
Electrophoretic Mobility Shift Assay
Female
Genetic Predisposition to Disease
Genotype
Hong Kong epidemiology
Humans
Risk Factors
Transcription Factors genetics
Transcription Factors metabolism
BRCA1 Protein genetics
Breast Neoplasms genetics
Polymorphism, Genetic genetics
Promoter Regions, Genetic genetics
Transcription, Genetic
Subjects
Details
- Language :
- English
- ISSN :
- 1468-6244
- Volume :
- 46
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Journal of medical genetics
- Publication Type :
- Academic Journal
- Accession number :
- 18782836
- Full Text :
- https://doi.org/10.1136/jmg.2007.057174