메뉴 건너뛰기




Volumn 225, Issue 4, 2011, Pages 535-543

Genetic polymorphisms in AURKA and BRCA1 are associated with breast cancer susceptibility in a Chinese Han population

Author keywords

AURKA; Aurora A; BRCA1; breast cancer; risk; SNP

Indexed keywords

AURORA A KINASE; BRCA1 PROTEIN;

EID: 81355147768     PISSN: 00223417     EISSN: 10969896     Source Type: Journal    
DOI: 10.1002/path.2902     Document Type: Article
Times cited : (38)

References (32)
  • 1
    • 0037685164 scopus 로고    scopus 로고
    • Breast and ovarian cancer
    • Wooster R, Weber BL,. Breast and ovarian cancer. N Engl J Med 2003; 348: 2339-2347.
    • (2003) N Engl J Med , vol.348 , pp. 2339-2347
    • Wooster, R.1    Weber, B.L.2
  • 2
    • 68649101805 scopus 로고    scopus 로고
    • Common vs. rare allele hypotheses for complex diseases
    • Schork NJ, Murray SS, Frazer KA, et al., Common vs. rare allele hypotheses for complex diseases. Curr Opin Genet Dev 2009; 19: 212-219.
    • (2009) Curr Opin Genet Dev , vol.19 , pp. 212-219
    • Schork, N.J.1    Murray, S.S.2    Frazer, K.A.3
  • 3
    • 18444369013 scopus 로고    scopus 로고
    • The structure of haplotype blocks in the human genome
    • Gabriel SB, Schaffner SF, Nguyen H, et al., The structure of haplotype blocks in the human genome. Science 2002; 296: 2225-2229.
    • (2002) Science , vol.296 , pp. 2225-2229
    • Gabriel, S.B.1    Schaffner, S.F.2    Nguyen, H.3
  • 4
    • 0043175289 scopus 로고    scopus 로고
    • Choosing haplotype-tagging SNPS based on unphased genotype data using a preliminary sample of unrelated subjects with an example from the multi-ethnic cohort study
    • Stram DO, Haiman CA, Hirschhorn JN, et al., Choosing haplotype-tagging SNPS based on unphased genotype data using a preliminary sample of unrelated subjects with an example from the multi-ethnic cohort study. Hum Hered 2003; 55: 27-36.
    • (2003) Hum Hered , vol.55 , pp. 27-36
    • Stram, D.O.1    Haiman, C.A.2    Hirschhorn, J.N.3
  • 5
    • 0034789532 scopus 로고    scopus 로고
    • Haplotype tagging for the identification of common disease genes
    • Johnson GC, Esposito L, Barratt BJ, et al., Haplotype tagging for the identification of common disease genes. Nat Genet 2001; 29: 233-237.
    • (2001) Nat Genet , vol.29 , pp. 233-237
    • Johnson, G.C.1    Esposito, L.2    Barratt, B.J.3
  • 6
    • 0034791035 scopus 로고    scopus 로고
    • High-resolution haplotype structure in the human genome
    • Daly MJ, Rioux JD, Schaffner SF, et al., High-resolution haplotype structure in the human genome. Nat Genet 2001; 29: 229-232.
    • (2001) Nat Genet , vol.29 , pp. 229-232
    • Daly, M.J.1    Rioux, J.D.2    Schaffner, S.F.3
  • 7
    • 13844313862 scopus 로고    scopus 로고
    • Whole-genome patterns of common DNA variation in three human populations
    • Hinds DA, Stuve LL, Nilsen GB, et al., Whole-genome patterns of common DNA variation in three human populations. Science 2005; 307: 1072-1079.
    • (2005) Science , vol.307 , pp. 1072-1079
    • Hinds, D.A.1    Stuve, L.L.2    Nilsen, G.B.3
  • 8
    • 23844522329 scopus 로고    scopus 로고
    • Haplotype analysis of common variants in the BRCA1 gene and risk of sporadic breast cancer
    • Cox DG, Kraft P, Hankinson SE, et al., Haplotype analysis of common variants in the BRCA1 gene and risk of sporadic breast cancer. Breast Cancer Res 2005; 7: R171-175.
    • (2005) Breast Cancer Res , vol.7
    • Cox, D.G.1    Kraft, P.2    Hankinson, S.E.3
  • 9
    • 34250188802 scopus 로고    scopus 로고
    • Common variants in the ATM, BRCA1, BRCA2, CHEK2 and TP53 cancer susceptibility genes are unlikely to increase breast cancer risk
    • Baynes C, Healey CS, Pooley KA, et al., Common variants in the ATM, BRCA1, BRCA2, CHEK2 and TP53 cancer susceptibility genes are unlikely to increase breast cancer risk. Breast Cancer Res 2007; 9: R27.
    • (2007) Breast Cancer Res , vol.9
    • Baynes, C.1    Healey, C.S.2    Pooley, K.A.3
  • 10
    • 51649095569 scopus 로고    scopus 로고
    • The Aurora kinase family in cell division and cancer
    • Vader G, Lens SM,. The Aurora kinase family in cell division and cancer. Biochim Biophys Acta 2008; 1786: 60-72.
    • (2008) Biochim Biophys Acta , vol.1786 , pp. 60-72
    • Vader, G.1    Lens, S.M.2
  • 11
    • 0031714080 scopus 로고    scopus 로고
    • Tumour amplified kinase STK15/BTAK induces centrosome amplification, aneuploidy and transformation
    • Zhou H, Kuang J, Zhong L, et al., Tumour amplified kinase STK15/BTAK induces centrosome amplification, aneuploidy and transformation. Nat Genet 1998; 20: 189-193.
    • (1998) Nat Genet , vol.20 , pp. 189-193
    • Zhou, H.1    Kuang, J.2    Zhong, L.3
  • 13
    • 37049023673 scopus 로고    scopus 로고
    • Aurora-A kinase regulates breast cancer associated gene 1 inhibition of centrosome-dependent microtubule nucleation
    • Sankaran S, Crone DE, Palazzo RE, et al., Aurora-A kinase regulates breast cancer associated gene 1 inhibition of centrosome-dependent microtubule nucleation. Cancer Res 2007; 67: 11186-11194.
    • (2007) Cancer Res , vol.67 , pp. 11186-11194
    • Sankaran, S.1    Crone, D.E.2    Palazzo, R.E.3
  • 14
    • 0037586498 scopus 로고    scopus 로고
    • AURORA-A amplification overrides the mitotic spindle assembly checkpoint, inducing resistance to Taxol
    • Anand S, Penrhyn-Lowe S, Venkitaraman AR,. AURORA-A amplification overrides the mitotic spindle assembly checkpoint, inducing resistance to Taxol. Cancer Cell 2003; 3: 51-62.
    • (2003) Cancer Cell , vol.3 , pp. 51-62
    • Anand, S.1    Penrhyn-Lowe, S.2    Venkitaraman, A.R.3
  • 16
    • 17844381081 scopus 로고    scopus 로고
    • Breast cancer risk associated with genotypic polymorphism of the mitosis-regulating gene Aurora-A/STK15/BTAK
    • Lo YL, Yu JC, Chen ST, et al., Breast cancer risk associated with genotypic polymorphism of the mitosis-regulating gene Aurora-A/STK15/BTAK. Int J Cancer 2005; 115: 276-283.
    • (2005) Int J Cancer , vol.115 , pp. 276-283
    • Lo, Y.L.1    Yu, J.C.2    Chen, S.T.3
  • 17
    • 0037069779 scopus 로고    scopus 로고
    • Prediction of the risk of myocardial infarction from polymorphisms in candidate genes
    • Yamada Y, Izawa H, Ichihara S, et al., Prediction of the risk of myocardial infarction from polymorphisms in candidate genes. N Engl J Med 2002; 347: 1916-1923.
    • (2002) N Engl J Med , vol.347 , pp. 1916-1923
    • Yamada, Y.1    Izawa, H.2    Ichihara, S.3
  • 18
    • 49849106302 scopus 로고    scopus 로고
    • Genetic factors for ischemic and hemorrhagic stroke in Japanese individuals
    • Yamada Y, Metoki N, Yoshida H, et al., Genetic factors for ischemic and hemorrhagic stroke in Japanese individuals. Stroke 2008; 39: 2211-2218.
    • (2008) Stroke , vol.39 , pp. 2211-2218
    • Yamada, Y.1    Metoki, N.2    Yoshida, H.3
  • 19
    • 0001677717 scopus 로고
    • Controlling the false discovery rate a practical and powerful approach to multiple testing
    • Benjamini Y, Hochberg Y,. Controlling the false discovery rate a practical and powerful approach to multiple testing. J Roy Statist Soc Ser B 1995; 57: 289-300.
    • (1995) J Roy Statist Soc ser B , vol.57 , pp. 289-300
    • Benjamini, Y.1    Hochberg, Y.2
  • 20
    • 8844241475 scopus 로고    scopus 로고
    • Functional Phe31Ile polymorphism in Aurora A and risk of breast carcinoma
    • Sun T, Miao X, Wang J, et al., Functional Phe31Ile polymorphism in Aurora A and risk of breast carcinoma. Carcinogenesis 2004; 25: 2225-2230.
    • (2004) Carcinogenesis , vol.25 , pp. 2225-2230
    • Sun, T.1    Miao, X.2    Wang, J.3
  • 21
    • 11144234946 scopus 로고    scopus 로고
    • Synergistic effects of STK15 gene polymorphisms and endogenous estrogen exposure in the risk of breast cancer
    • Dai Q, Cai QY, Shu XO, et al., Synergistic effects of STK15 gene polymorphisms and endogenous estrogen exposure in the risk of breast cancer. Cancer Epidemiol Biomarkers Prev 2004; 13: 2065-2070.
    • (2004) Cancer Epidemiol Biomarkers Prev , vol.13 , pp. 2065-2070
    • Dai, Q.1    Cai, Q.Y.2    Shu, X.O.3
  • 22
    • 33746768935 scopus 로고    scopus 로고
    • Inconsistent association between the STK15 F31I genetic polymorphism and breast cancer risk
    • Fletcher O, Johnson N, Palles C, et al., Inconsistent association between the STK15 F31I genetic polymorphism and breast cancer risk. J Natl Cancer Inst 2006; 98: 1014-1018.
    • (2006) J Natl Cancer Inst , vol.98 , pp. 1014-1018
    • Fletcher, O.1    Johnson, N.2    Palles, C.3
  • 23
    • 24944573674 scopus 로고    scopus 로고
    • Aurora-A STK15 T91A is a general low penetrance cancer susceptibility gene: A meta-analysis of multiple cancer types
    • Ewart-Toland A, Dai Q, Gao YT, et al., Aurora-A STK15 T91A is a general low penetrance cancer susceptibility gene: a meta-analysis of multiple cancer types. Carcinogenesis 2005; 26: 1368-1373.
    • (2005) Carcinogenesis , vol.26 , pp. 1368-1373
    • Ewart-Toland, A.1    Dai, Q.2    Gao, Y.T.3
  • 24
    • 0042093747 scopus 로고    scopus 로고
    • Identification of Stk6/STK15 as a candidate low penetrance tumor-susceptibility gene in mouse and human
    • Ewart-Toland A, Briassouli P, de Koning JP, et al., Identification of Stk6/STK15 as a candidate low penetrance tumor-susceptibility gene in mouse and human. Nat Genet 2003; 34: 403-412.
    • (2003) Nat Genet , vol.34 , pp. 403-412
    • Ewart-Toland, A.1    Briassouli, P.2    De Koning, J.P.3
  • 25
    • 77956635748 scopus 로고    scopus 로고
    • The influence of common polymorphisms on breast cancer
    • Eccles D, Tapper W,. The influence of common polymorphisms on breast cancer. Cancer Treat Res 2010; 155: 15-32.
    • (2010) Cancer Treat Res , vol.155 , pp. 15-32
    • Eccles, D.1    Tapper, W.2
  • 26
    • 0036906745 scopus 로고    scopus 로고
    • Haplotype and linkage disequilibrium architecture for human cancer-associated genes
    • Bonnen PE, Wang PJ, Kimmel M, et al., Haplotype and linkage disequilibrium architecture for human cancer-associated genes. Genome Res 2002; 12: 1846-1853.
    • (2002) Genome Res , vol.12 , pp. 1846-1853
    • Bonnen, P.E.1    Wang, P.J.2    Kimmel, M.3
  • 27
    • 23844475353 scopus 로고    scopus 로고
    • A haplotype-based case-control study of BRCA1 and sporadic breast cancer risk
    • Freedman ML, Penney KL, Stram DO, et al., A haplotype-based case-control study of BRCA1 and sporadic breast cancer risk. Cancer Res 2005; 65: 7516-7522.
    • (2005) Cancer Res , vol.65 , pp. 7516-7522
    • Freedman, M.L.1    Penney, K.L.2    Stram, D.O.3
  • 28
    • 56649094379 scopus 로고    scopus 로고
    • Mutation screening of the BRCA1 gene in sporadic breast cancer in southern Chinese populations
    • Haitian Z, Yunfei L, Jian Z, et al., Mutation screening of the BRCA1 gene in sporadic breast cancer in southern Chinese populations. Breast 2008; 17: 563-567.
    • (2008) Breast , vol.17 , pp. 563-567
    • Haitian, Z.1    Yunfei, L.2    Jian, Z.3
  • 29
    • 33748149196 scopus 로고    scopus 로고
    • The prevalence of BRCA1 and BRCA2 mutations in eastern Chinese women with breast cancer
    • Song CG, Hu Z, Wu J, et al., The prevalence of BRCA1 and BRCA2 mutations in eastern Chinese women with breast cancer. J Cancer Res Clin Oncol 2006; 132: 617-626.
    • (2006) J Cancer Res Clin Oncol , vol.132 , pp. 617-626
    • Song, C.G.1    Hu, Z.2    Wu, J.3
  • 31
    • 33847099142 scopus 로고    scopus 로고
    • SNP-SNP interactions in breast cancer susceptibility
    • Onay VU, Briollais L, Knight JA, et al., SNP-SNP interactions in breast cancer susceptibility. BMC Cancer 2006; 6: 114.
    • (2006) BMC Cancer , vol.6 , pp. 114
    • Onay, V.U.1    Briollais, L.2    Knight, J.A.3
  • 32
    • 59049101918 scopus 로고    scopus 로고
    • Genetic variants of BLM interact with RAD51 to increase breast cancer susceptibility
    • Ding SL, Yu JC, Chen ST, et al., Genetic variants of BLM interact with RAD51 to increase breast cancer susceptibility. Carcinogenesis 2009; 30: 43-49.
    • (2009) Carcinogenesis , vol.30 , pp. 43-49
    • Ding, S.L.1    Yu, J.C.2    Chen, S.T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.