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Article: Functional polymorphisms in the BRCA1 promoter influence transcription and are associated with decreased risk for breast cancer in Chinese women
Title | Functional polymorphisms in the BRCA1 promoter influence transcription and are associated with decreased risk for breast cancer in Chinese women | ||||||||
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Authors | |||||||||
Issue Date | 2009 | ||||||||
Publisher | BMJ Group. The Journal's web site is located at http://jmg.bmj.com/ | ||||||||
Citation | Journal Of Medical Genetics, 2009, v. 46 n. 1, p. 32-39 How to Cite? | ||||||||
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. 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% Cl 0.69 to 0.93; p = 0.003) which was more evident among women aged ≥45 years at first diagnosis of breast cancer and without a family history of breast cancer (combined OR = 0.75, 95% Cl 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 ≥45 years without a family history of breast cancer (OR = 0.64, 95% Cl 0.46 to 0.89; p = 0.008). 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. | ||||||||
Persistent Identifier | http://hdl.handle.net/10722/58601 | ||||||||
ISSN | 2023 Impact Factor: 3.5 2023 SCImago Journal Rankings: 1.690 | ||||||||
PubMed Central ID | |||||||||
ISI Accession Number ID |
Funding Information: This study was funded by the Research Grant Council, Hong Kong SAR, China, (project code HKU 7520/05M) and the Committee on Research and Conference Grants from the University of Hong Kong (project code 200711159018). The Shanghai Breast Cancer Study is supported by RO1CA64277 and RO1CA90899 from the National Cancer Institute. | ||||||||
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DC Field | Value | Language |
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dc.contributor.author | Chan, KYK | en_HK |
dc.contributor.author | Liu, W | en_HK |
dc.contributor.author | Long, JR | en_HK |
dc.contributor.author | Yip, SP | en_HK |
dc.contributor.author | Chan, SY | en_HK |
dc.contributor.author | Shu, XO | en_HK |
dc.contributor.author | Chua, DTT | en_HK |
dc.contributor.author | Cheung, ANY | en_HK |
dc.contributor.author | Ching, JCY | en_HK |
dc.contributor.author | Cai, H | en_HK |
dc.contributor.author | Au, GKH | en_HK |
dc.contributor.author | Chan, M | en_HK |
dc.contributor.author | Foo, W | en_HK |
dc.contributor.author | Ngan, HYS | en_HK |
dc.contributor.author | Gao, YT | en_HK |
dc.contributor.author | Ngan, ESW | en_HK |
dc.contributor.author | GarciaBarceló, MM | en_HK |
dc.contributor.author | Zheng, W | en_HK |
dc.contributor.author | Khoo, US | en_HK |
dc.date.accessioned | 2010-05-31T03:33:17Z | - |
dc.date.available | 2010-05-31T03:33:17Z | - |
dc.date.issued | 2009 | en_HK |
dc.identifier.citation | Journal Of Medical Genetics, 2009, v. 46 n. 1, p. 32-39 | en_HK |
dc.identifier.issn | 0022-2593 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/58601 | - |
dc.description.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. 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% Cl 0.69 to 0.93; p = 0.003) which was more evident among women aged ≥45 years at first diagnosis of breast cancer and without a family history of breast cancer (combined OR = 0.75, 95% Cl 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 ≥45 years without a family history of breast cancer (OR = 0.64, 95% Cl 0.46 to 0.89; p = 0.008). 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. | en_HK |
dc.language | eng | en_HK |
dc.publisher | BMJ Group. The Journal's web site is located at http://jmg.bmj.com/ | en_HK |
dc.relation.ispartof | Journal of Medical Genetics | en_HK |
dc.subject.mesh | BRCA1 Protein - genetics | - |
dc.subject.mesh | Breast Neoplasms - epidemiology - genetics | - |
dc.subject.mesh | Polymorphism, Genetic - genetics | - |
dc.subject.mesh | Promoter Regions, Genetic - genetics | - |
dc.subject.mesh | Transcription, Genetic | - |
dc.title | Functional polymorphisms in the BRCA1 promoter influence transcription and are associated with decreased risk for breast cancer in Chinese women | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0022-2593&volume=46&spage=32&epage=39&date=2009&atitle=Functional+polymorphisms+in+the+BRCA1+promoter+influence+transcription+and+are+associated+with+decreased+risk+for+breast+cancer+in+Chinese+women. | en_HK |
dc.identifier.email | Chan, KYK: kelvinc@pathology.hku.hk | en_HK |
dc.identifier.email | Chua, DTT: dttchua@hkucc.hku.hk | en_HK |
dc.identifier.email | Cheung, ANY: anycheun@hkucc.hku.hk | en_HK |
dc.identifier.email | Ngan, HYS: hysngan@hkucc.hku.hk | en_HK |
dc.identifier.email | Ngan, ESW: engan@hku.hk | en_HK |
dc.identifier.email | GarciaBarceló, MM: mmgarcia@hku.hk | en_HK |
dc.identifier.email | Khoo, US: uskhoo@hku.hk | en_HK |
dc.identifier.authority | Chan, KYK=rp00453 | en_HK |
dc.identifier.authority | Chua, DTT=rp00415 | en_HK |
dc.identifier.authority | Cheung, ANY=rp00542 | en_HK |
dc.identifier.authority | Ngan, HYS=rp00346 | en_HK |
dc.identifier.authority | Ngan, ESW=rp00422 | en_HK |
dc.identifier.authority | GarciaBarceló, MM=rp00445 | en_HK |
dc.identifier.authority | Khoo, US=rp00362 | en_HK |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1136/jmg.2007.057174 | en_HK |
dc.identifier.pmid | 18782836 | - |
dc.identifier.pmcid | PMC2782922 | - |
dc.identifier.scopus | eid_2-s2.0-58549086564 | en_HK |
dc.identifier.hkuros | 166040 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-58549086564&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 46 | en_HK |
dc.identifier.issue | 1 | en_HK |
dc.identifier.spage | 32 | en_HK |
dc.identifier.epage | 39 | en_HK |
dc.identifier.eissn | 1468-6244 | - |
dc.identifier.isi | WOS:000262198000005 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.relation.project | Gene-based and haplotype analysis of the estrogen receptor genes for breast cancer susceptibility | - |
dc.identifier.scopusauthorid | Chan, KYK=7406034195 | en_HK |
dc.identifier.scopusauthorid | Liu, W=36078432200 | en_HK |
dc.identifier.scopusauthorid | Long, JR=7403446542 | en_HK |
dc.identifier.scopusauthorid | Yip, SP=7102133673 | en_HK |
dc.identifier.scopusauthorid | Chan, SY=36466096800 | en_HK |
dc.identifier.scopusauthorid | Shu, XO=7102525083 | en_HK |
dc.identifier.scopusauthorid | Chua, DTT=7006773480 | en_HK |
dc.identifier.scopusauthorid | Cheung, ANY=54927484100 | en_HK |
dc.identifier.scopusauthorid | Ching, JCY=15735635300 | en_HK |
dc.identifier.scopusauthorid | Cai, H=12802855000 | en_HK |
dc.identifier.scopusauthorid | Au, GKH=7003748615 | en_HK |
dc.identifier.scopusauthorid | Chan, M=7402597760 | en_HK |
dc.identifier.scopusauthorid | Foo, W=7003318564 | en_HK |
dc.identifier.scopusauthorid | Ngan, HYS=34571944100 | en_HK |
dc.identifier.scopusauthorid | Gao, YT=34770682500 | en_HK |
dc.identifier.scopusauthorid | Ngan, ESW=22234827500 | en_HK |
dc.identifier.scopusauthorid | GarciaBarceló, MM=6701767303 | en_HK |
dc.identifier.scopusauthorid | Zheng, W=35381589100 | en_HK |
dc.identifier.scopusauthorid | Khoo, US=7004195799 | en_HK |
dc.identifier.issnl | 0022-2593 | - |