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Erschienen in: Journal of Cancer Research and Clinical Oncology 11/2009

01.11.2009 | Original Paper

Polymorphisms in BRCA1, BRCA1-interacting genes and susceptibility of breast cancer in Chinese women

verfasst von: Xiang Huo, Cheng Lu, Xinen Huang, Zhibin Hu, Guangfu Jin, Hongxia Ma, Xuechen Wang, Jianwei Qin, Xinru Wang, Hongbing Shen, Jinhai Tang

Erschienen in: Journal of Cancer Research and Clinical Oncology | Ausgabe 11/2009

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Abstract

Purpose

BRCA1-interacting protein C-terminal helicase 1 (BRIP1) and zinc finger protein 350 (ZNF350) work with BRCA1 in tumor suppression procedures. Low penetrance variants of these three genes may jointly affect individuals’ breast cancer susceptibility in general population.

Methods

We focused on potentially functional single nucleotide polymorphisms (SNPs) in the coding regions of BRIP1, ZNF350 and BRCA1 and pairwise-tagging approach was used to minimize the number of SNPs. Five SNPs were selected and genotyped by PCR-restriction fraction length polymorphism or PCR-primer introduced restriction analysis assays in a case–control study with 568 breast cancer cases and 624 controls in a Chinese population.

Results

All of the five SNPs except rs2278415 of ZNF350 conferred a modestly increased risk, although, with no statistical significance. Joint effect analyses indicated that all the variant genotypes of ZNF350 polymorphisms accounted for increased breast cancer risk among subjects carrying variant homozygote of BRCA1 rs799917, particularly for ZNF350 rs4986773 (OR = 2.03, 95%CI = 1.02–4.05, the test for gene–gene interaction P int = 0.059).

Conclusion

BRCA1 and ZNF350 may jointly contribute to individuals’ susceptibility of breast cancer in Chinese women. Further functional studies are warranted to validate our findings.
Literatur
Zurück zum Zitat Bhatti P, Church DM, Rutter JL, Struewing JP, Sigurdson AJ (2006) Candidate single nucleotide polymorphism selection using publicly available tools: a guide for epidemiologists. Am J Epidemiol 164(8):794–804. doi:10.1093/aje/kwj269 PubMedCrossRef Bhatti P, Church DM, Rutter JL, Struewing JP, Sigurdson AJ (2006) Candidate single nucleotide polymorphism selection using publicly available tools: a guide for epidemiologists. Am J Epidemiol 164(8):794–804. doi:10.​1093/​aje/​kwj269 PubMedCrossRef
Zurück zum Zitat Dunning AM, Chiano M, Smith NR, Dearden J, Gore M, Oakes S et al (1997) Common BRCA1 variants and susceptibility to breast and ovarian cancer in the general population. Hum Mol Genet 6(2):285–289. doi:10.1093/hmg/6.2.285 PubMedCrossRef Dunning AM, Chiano M, Smith NR, Dearden J, Gore M, Oakes S et al (1997) Common BRCA1 variants and susceptibility to breast and ovarian cancer in the general population. Hum Mol Genet 6(2):285–289. doi:10.​1093/​hmg/​6.​2.​285 PubMedCrossRef
Zurück zum Zitat Eelen G, Vanden Bempt I, Verlinden L, Drijkoningen M, Smeets A, Neven P et al (2008) Expression of the BRCA1-interacting protein BRIP1/BACH1/FANCJ is driven by E2F and correlates with human breast cancer malignancy. Oncogene [Epub ahead of print] Eelen G, Vanden Bempt I, Verlinden L, Drijkoningen M, Smeets A, Neven P et al (2008) Expression of the BRCA1-interacting protein BRIP1/BACH1/FANCJ is driven by E2F and correlates with human breast cancer malignancy. Oncogene [Epub ahead of print]
Zurück zum Zitat Ford D, Easton DF, Peto J (1995) Estimates of the gene frequency of BRCA1 and its contribution to breast and ovarian cancer incidence. Am J Hum Genet 57(6):1457–1462PubMed Ford D, Easton DF, Peto J (1995) Estimates of the gene frequency of BRCA1 and its contribution to breast and ovarian cancer incidence. Am J Hum Genet 57(6):1457–1462PubMed
Zurück zum Zitat Furuta S, Wang JM, Wei S, Jeng YM, Jiang X, Gu B et al (2006) Removal of BRCA1/CtIP/ZBRK1 repressor complex on ANG1 promoter leads to accelerated mammary tumor growth contributed by prominent vasculature. Cancer Cell 10(1):13–24PubMedCrossRef Furuta S, Wang JM, Wei S, Jeng YM, Jiang X, Gu B et al (2006) Removal of BRCA1/CtIP/ZBRK1 repressor complex on ANG1 promoter leads to accelerated mammary tumor growth contributed by prominent vasculature. Cancer Cell 10(1):13–24PubMedCrossRef
Zurück zum Zitat García-Closas M, Egan KM, Newcomb PA, Brinton LA, Titus-Ernstoff L, Chanock S et al (2006) Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: two population-based studies in USA and Poland, and meta-analyses. Hum Genet 119(4):376–388. doi:10.1007/s00439-006-0135-z PubMedCrossRef García-Closas M, Egan KM, Newcomb PA, Brinton LA, Titus-Ernstoff L, Chanock S et al (2006) Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: two population-based studies in USA and Poland, and meta-analyses. Hum Genet 119(4):376–388. doi:10.​1007/​s00439-006-0135-z PubMedCrossRef
Zurück zum Zitat Huo X, Hu Z, Zhai X, Wang Y, Wang S, Wang X et al (2007) Common non-synonymous polymorphisms in the BRCA1 Associated RING Domain (BARD1) gene are associated with breast cancer susceptibility: a case–control analysis. Breast Cancer Res Treat 102(3):329–337. doi:10.1007/s10549-006-9332-7 PubMedCrossRef Huo X, Hu Z, Zhai X, Wang Y, Wang S, Wang X et al (2007) Common non-synonymous polymorphisms in the BRCA1 Associated RING Domain (BARD1) gene are associated with breast cancer susceptibility: a case–control analysis. Breast Cancer Res Treat 102(3):329–337. doi:10.​1007/​s10549-006-9332-7 PubMedCrossRef
Zurück zum Zitat Rutter JL, Smith AM, Dávila MR, Sigurdson AJ, Giusti RM, Pineda MA et al (2003) Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2-negative probands from breast-ovarian cancer families and among early-onset breast cancer cases and reference individuals. Hum Mutat 22(2):121–128. doi:10.1002/humu.10238 PubMedCrossRef Rutter JL, Smith AM, Dávila MR, Sigurdson AJ, Giusti RM, Pineda MA et al (2003) Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2-negative probands from breast-ovarian cancer families and among early-onset breast cancer cases and reference individuals. Hum Mutat 22(2):121–128. doi:10.​1002/​humu.​10238 PubMedCrossRef
Zurück zum Zitat Sigurdson AJ, Hauptmann M, Chatterjee N, Alexander BH, Doody MM, Rutter JL et al (2004) Kin-cohort estimates for familial breast cancer risk in relation to variants in DNA base excision repair, BRCA1 interacting and growth factor genes. BMC Cancer 4:9. doi:10.1186/1471-2407-4-9 PubMedCrossRef Sigurdson AJ, Hauptmann M, Chatterjee N, Alexander BH, Doody MM, Rutter JL et al (2004) Kin-cohort estimates for familial breast cancer risk in relation to variants in DNA base excision repair, BRCA1 interacting and growth factor genes. BMC Cancer 4:9. doi:10.​1186/​1471-2407-4-9 PubMedCrossRef
Zurück zum Zitat Soucek P, Borovanova T, Pohlreich P, Kleibl Z, Novotny J (2007) Role of single nucleotide polymorphisms and haplotypes in BRCA1 in breast cancer: Czech case–control study. Breast Cancer Res Treat 103(2):219–224. doi:10.1007/s10549-006-9367-9 PubMedCrossRef Soucek P, Borovanova T, Pohlreich P, Kleibl Z, Novotny J (2007) Role of single nucleotide polymorphisms and haplotypes in BRCA1 in breast cancer: Czech case–control study. Breast Cancer Res Treat 103(2):219–224. doi:10.​1007/​s10549-006-9367-9 PubMedCrossRef
Metadaten
Titel
Polymorphisms in BRCA1, BRCA1-interacting genes and susceptibility of breast cancer in Chinese women
verfasst von
Xiang Huo
Cheng Lu
Xinen Huang
Zhibin Hu
Guangfu Jin
Hongxia Ma
Xuechen Wang
Jianwei Qin
Xinru Wang
Hongbing Shen
Jinhai Tang
Publikationsdatum
01.11.2009
Verlag
Springer-Verlag
Erschienen in
Journal of Cancer Research and Clinical Oncology / Ausgabe 11/2009
Print ISSN: 0171-5216
Elektronische ISSN: 1432-1335
DOI
https://doi.org/10.1007/s00432-009-0604-6

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