메뉴 건너뛰기




Volumn 220, Issue 2, 2005, Pages 177-184

High frequency of somatic missense mutation of BRCA2 in female breast cancer from Taiwan

Author keywords

BRCA2; Breast cancer; Somatic mutation; Taiwan

Indexed keywords

BRCA2 PROTEIN; NUCLEOTIDE; RAD51 PROTEIN;

EID: 17644411687     PISSN: 03043835     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.canlet.2004.10.024     Document Type: Article
Times cited : (8)

References (40)
  • 2
    • 17344365851 scopus 로고    scopus 로고
    • Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. the Breast Cancer Linkage Consortium
    • D. Ford, D.F. Easton, M. Stratton, S. Narod, D. Goldgar, and P. Devilee Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium Am. J. Hum. Genet. 62 1998 676 689
    • (1998) Am. J. Hum. Genet. , vol.62 , pp. 676-689
    • Ford, D.1    Easton, D.F.2    Stratton, M.3    Narod, S.4    Goldgar, D.5    Devilee, P.6
  • 3
    • 0037169354 scopus 로고    scopus 로고
    • Cancer susceptibility and the functions of BRCA1 and BRCA2
    • A.R. Venkitaraman Cancer susceptibility and the functions of BRCA1 and BRCA2 Cell 108 2002 171 182
    • (2002) Cell , vol.108 , pp. 171-182
    • Venkitaraman, A.R.1
  • 8
  • 9
    • 0029820321 scopus 로고    scopus 로고
    • A somatic truncating mutation in BRCA2 in a sporadic breast tumor
    • B.H. Weber, M. Brohm, I. Stec, J. Backe, and H. Caffier A somatic truncating mutation in BRCA2 in a sporadic breast tumor Am. J. Hum. Genet. 59 1996 962 964
    • (1996) Am. J. Hum. Genet. , vol.59 , pp. 962-964
    • Weber, B.H.1    Brohm, M.2    Stec, I.3    Backe, J.4    Caffier, H.5
  • 10
    • 0029905138 scopus 로고    scopus 로고
    • Allelic loss at chromosome 13q12-q13 is associated with poor prognosis in familial and sporadic breast cancer
    • J. van den Berg, O. Johannsson, S. Hakansson, H. Olsson, and A. Borg Allelic loss at chromosome 13q12-q13 is associated with poor prognosis in familial and sporadic breast cancer Br. J. Cancer 74 1996 1615 1619
    • (1996) Br. J. Cancer , vol.74 , pp. 1615-1619
    • Van Den Berg, J.1    Johannsson, O.2    Hakansson, S.3    Olsson, H.4    Borg, A.5
  • 11
    • 8544224972 scopus 로고    scopus 로고
    • Genomic deletions in the BRCA1, BRCA2 and TP53 regions associate with low expression of the estrogen receptor in sporadic breast carcinoma
    • R.K. Schmutzler, E. Bierhoff, T. Werkhausen, R. Fimmers, P. Speiser, and E. Kubista Genomic deletions in the BRCA1, BRCA2 and TP53 regions associate with low expression of the estrogen receptor in sporadic breast carcinoma Int. J. Cancer 74 1997 322 325
    • (1997) Int. J. Cancer , vol.74 , pp. 322-325
    • Schmutzler, R.K.1    Bierhoff, E.2    Werkhausen, T.3    Fimmers, R.4    Speiser, P.5    Kubista, E.6
  • 12
    • 0033814025 scopus 로고    scopus 로고
    • Association between loss of heterozygosity of BRCA1 and BRCA2 and morphological attributes of sporadic breast cancer
    • A. Hanby, D.P. Kelsell, H. Potts, C.E. Gillett, D.T. Bishop, N.K. Spurr, and D.M. Barnes Association between loss of heterozygosity of BRCA1 and BRCA2 and morphological attributes of sporadic breast cancer Int. J. Cancer 88 2000 204 208
    • (2000) Int. J. Cancer , vol.88 , pp. 204-208
    • Hanby, A.1    Kelsell, D.P.2    Potts, H.3    Gillett, C.E.4    Bishop, D.T.5    Spurr, N.K.6    Barnes, D.M.7
  • 13
    • 0030923394 scopus 로고    scopus 로고
    • Karnofsky Memorial Lecture. Hereditary cancer: Theme and variations
    • A.G. Knudson Karnofsky Memorial Lecture. Hereditary cancer: theme and variations J. Clin. Oncol. 15 1997 3280 3287
    • (1997) J. Clin. Oncol. , vol.15 , pp. 3280-3287
    • Knudson, A.G.1
  • 14
    • 1642618293 scopus 로고    scopus 로고
    • EMSY, a BRCA-2 partner in crime
    • D.M. Livingston EMSY, a BRCA-2 partner in crime Nat. Med. 10 2004 127 128
    • (2004) Nat. Med. , vol.10 , pp. 127-128
    • Livingston, D.M.1
  • 15
    • 0033866487 scopus 로고    scopus 로고
    • The breast cancer information core: Database design, structure and scope
    • C.I. Szabo, A. Masiello, J.F. Ryan, and L.C. Brody The breast cancer information core: database design, structure and scope Hum. Mut. 16 2000 123 131
    • (2000) Hum. Mut. , vol.16 , pp. 123-131
    • Szabo, C.I.1    Masiello, A.2    Ryan, J.F.3    Brody, L.C.4
  • 16
    • 0030902227 scopus 로고    scopus 로고
    • Population genetics of BRCA1 and BRCA2
    • C.I. Szabo, and M.C. King Population genetics of BRCA1 and BRCA2 Am. J. Hum. Genet. 60 1997 1013 1020
    • (1997) Am. J. Hum. Genet. , vol.60 , pp. 1013-1020
    • Szabo, C.I.1    King, M.C.2
  • 17
    • 0036450901 scopus 로고    scopus 로고
    • Hereditary breast and ovarian cancer in Asia: Genetic epidemiology of BRCA1 and BRCA2
    • A. Liede, and S.A. Narod Hereditary breast and ovarian cancer in Asia: genetic epidemiology of BRCA1 and BRCA2 Hum. Mutat. 20 2002 413 424
    • (2002) Hum. Mutat. , vol.20 , pp. 413-424
    • Liede, A.1    Narod, S.A.2
  • 20
    • 0012208349 scopus 로고    scopus 로고
    • Department of Health, Taiwan
    • Health Statistics, Department of Health, Taiwan, 2000.
    • (2000) Health Statistics
  • 21
    • 1842473022 scopus 로고    scopus 로고
    • High frequency of G/C transversion on p53 gene alterations in breast cancers from Taiwan
    • F.M. Chen, M. Hou, J.Y. Wang, T.C. Chen, D.C. Chen, and S.Y. Huang High frequency of G/C transversion on p53 gene alterations in breast cancers from Taiwan Cancer Lett. 207 2004 59 67
    • (2004) Cancer Lett. , vol.207 , pp. 59-67
    • Chen, F.M.1    Hou, M.2    Wang, J.Y.3    Chen, T.C.4    Chen, D.C.5    Huang, S.Y.6
  • 22
    • 0032908832 scopus 로고    scopus 로고
    • Molecular characterization of germline mutations in the BRCA1 and BRCA2 genes from breast cancer families in Taiwan
    • S.S. Li, H.M. Tseng, T.P. Yang, C.H. Liu, S.J. Teng, and H.W. Huang Molecular characterization of germline mutations in the BRCA1 and BRCA2 genes from breast cancer families in Taiwan Hum. Genet. 104 1999 201 204
    • (1999) Hum. Genet. , vol.104 , pp. 201-204
    • Li, S.S.1    Tseng, H.M.2    Yang, T.P.3    Liu, C.H.4    Teng, S.J.5    Huang, H.W.6
  • 23
    • 0031466027 scopus 로고    scopus 로고
    • RAD51 interacts with the evolutionarily conserved BRC motifs in the human breast cancer susceptibility gene brca2
    • A.K. Wong, R. Pero, P.A. Ormonde, S.V. Tavtigian, and P.L. Bartel RAD51 interacts with the evolutionarily conserved BRC motifs in the human breast cancer susceptibility gene brca2 J. Biol. Chem. 272 1997 31941 31944
    • (1997) J. Biol. Chem. , vol.272 , pp. 31941-31944
    • Wong, A.K.1    Pero, R.2    Ormonde, P.A.3    Tavtigian, S.V.4    Bartel, P.L.5
  • 27
    • 0033987736 scopus 로고    scopus 로고
    • Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion
    • J.T. Dunnen, and S.E. Antonarakis Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion Hum. Mutat. 15 2000 7 12
    • (2000) Hum. Mutat. , vol.15 , pp. 7-12
    • Dunnen, J.T.1    Antonarakis, S.E.2
  • 28
    • 0031831409 scopus 로고    scopus 로고
    • Frequent loss of heterozygosity at chromosome 13q12-13 with BRCA2 markers in sporadic male breast cancer
    • D. Prechtel, A.K. Werenskiold, K. Prechtel, G. Keller, and H. Hofler Frequent loss of heterozygosity at chromosome 13q12-13 with BRCA2 markers in sporadic male breast cancer Diag. Mol. Pathol. 7 1998 57 62
    • (1998) Diag. Mol. Pathol. , vol.7 , pp. 57-62
    • Prechtel, D.1    Werenskiold, A.K.2    Prechtel, K.3    Keller, G.4    Hofler, H.5
  • 29
    • 0037140117 scopus 로고    scopus 로고
    • Somatic mutations in the BRCA2 gene and high frequency of allelic loss of BRCA2 in sporadic male breast cancer
    • E. Kwiatkowska, M. Teresiak, D. Breborowicz, and A. Mackiewicz Somatic mutations in the BRCA2 gene and high frequency of allelic loss of BRCA2 in sporadic male breast cancer Int. J. Cancer 98 2002 943 945
    • (2002) Int. J. Cancer , vol.98 , pp. 943-945
    • Kwiatkowska, E.1    Teresiak, M.2    Breborowicz, D.3    MacKiewicz, A.4
  • 30
    • 0032953368 scopus 로고    scopus 로고
    • A somatic BRCA2 mutation in RER_ endometrial carcinomas that specifically deletes the amino-terminal transactivation domain
    • A. Koul, M. Nilbert, and A. Borg A somatic BRCA2 mutation in RER_ endometrial carcinomas that specifically deletes the amino-terminal transactivation domain Genes Chrom. Cancer 24 1999 207 212
    • (1999) Genes Chrom. Cancer , vol.24 , pp. 207-212
    • Koul, A.1    Nilbert, M.2    Borg, A.3
  • 31
    • 0142090694 scopus 로고    scopus 로고
    • High frequency of activated K-ras codon 15 mutant in colorectal carcinomas from Taiwanese patients
    • J.Y. Wang, J.S. Hsieh, F.M. Chen, C.S. Yeh, K. Alexandersen, and T.J. Huang High frequency of activated K-ras codon 15 mutant in colorectal carcinomas from Taiwanese patients Int. J. Cancer 107 2003 387 393
    • (2003) Int. J. Cancer , vol.107 , pp. 387-393
    • Wang, J.Y.1    Hsieh, J.S.2    Chen, F.M.3    Yeh, C.S.4    Alexandersen, K.5    Huang, T.J.6
  • 32
    • 0037051084 scopus 로고    scopus 로고
    • Sporadic breast cancer in young women: Prevalence of loss of heterozygosity at p53, BRCA1 and BRCA2
    • S.M. Johnson, J.A. Shaw, and R.A. Walker Sporadic breast cancer in young women: prevalence of loss of heterozygosity at p53, BRCA1 and BRCA2 Int. J. Cancer 98 2002 205 209
    • (2002) Int. J. Cancer , vol.98 , pp. 205-209
    • Johnson, S.M.1    Shaw, J.A.2    Walker, R.A.3
  • 33
    • 0342940785 scopus 로고    scopus 로고
    • Pathology of familial breast cancer: Differences between breast cancers in carriers of BRCA1 or BRCA2 mutations and sporadic cases
    • Breast Cancer Linkage Consortium Pathology of familial breast cancer: differences between breast cancers in carriers of BRCA1 or BRCA2 mutations and sporadic cases Lancet 349 1997 1505 1510
    • (1997) Lancet , vol.349 , pp. 1505-1510
    • Cancer Linkage Consortium, B.1
  • 34
    • 85010791733 scopus 로고    scopus 로고
    • A combined analysis of outcome following breast cancer: Differences in survival based on BRCA1/BRCA2 mutation status and administration of adjuvant treatment
    • M.E. Robson, P.O. Chappuis, J. Satagopan, N. Wong, J. Boyd, and J.R. Goffin A combined analysis of outcome following breast cancer: differences in survival based on BRCA1/BRCA2 mutation status and administration of adjuvant treatment Breast Cancer Res. 6 2004 R8 R17
    • (2004) Breast Cancer Res. , vol.6
    • Robson, M.E.1    Chappuis, P.O.2    Satagopan, J.3    Wong, N.4    Boyd, J.5    Goffin, J.R.6
  • 35
    • 0029794992 scopus 로고    scopus 로고
    • Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2
    • B.B. Roa, A.A. Boyd, K. Volcik, and C.S. Richards Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2 Nat. Genet. 14 1996 185 187
    • (1996) Nat. Genet. , vol.14 , pp. 185-187
    • Roa, B.B.1    Boyd, A.A.2    Volcik, K.3    Richards, C.S.4
  • 36
    • 18444364814 scopus 로고    scopus 로고
    • Incidence of non-founder BRCA1 and BRCA2 mutations in high risk Ashkenazi breast and ovarian cancer families
    • N.D. Kauff, P. Perez-Segura, M.E. Robson, L. Scheuer, B. Siegel, and A. Schluger Incidence of non-founder BRCA1 and BRCA2 mutations in high risk Ashkenazi breast and ovarian cancer families J. Med. Genet. 39 2002 611 614
    • (2002) J. Med. Genet. , vol.39 , pp. 611-614
    • Kauff, N.D.1    Perez-Segura, P.2    Robson, M.E.3    Scheuer, L.4    Siegel, B.5    Schluger, A.6
  • 37
    • 0031971484 scopus 로고    scopus 로고
    • Using gene carrier probability to select high risk families for identifying germline mutations in breast cancer susceptibility genes
    • J. Chang-Claude, J. Dong, S. Schmidt, M. Shayeghi, D. Komitowski, and H. Becher Using gene carrier probability to select high risk families for identifying germline mutations in breast cancer susceptibility genes J. Med. Genet. 35 1998 116 121
    • (1998) J. Med. Genet. , vol.35 , pp. 116-121
    • Chang-Claude, J.1    Dong, J.2    Schmidt, S.3    Shayeghi, M.4    Komitowski, D.5    Becher, H.6
  • 38
    • 0031917403 scopus 로고    scopus 로고
    • Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2
    • G. Parmigiani, D. Berry, and O. Aguilar Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2 Am. J. Hum. Genet. 62 1998 145 158
    • (1998) Am. J. Hum. Genet. , vol.62 , pp. 145-158
    • Parmigiani, G.1    Berry, D.2    Aguilar, O.3
  • 39
    • 0031832541 scopus 로고    scopus 로고
    • Sequence analysis of BRCA1 and BRCA2: Correlation of mutations with family history and ovarian cancer risk
    • T.S. Frank, S.A. Manley, O.I. Olopade, S. Cummings, J.E. Garber, and B. Bernhardt Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk J. Clin. Oncol. 16 1998 2417 2425
    • (1998) J. Clin. Oncol. , vol.16 , pp. 2417-2425
    • Frank, T.S.1    Manley, S.A.2    Olopade, O.I.3    Cummings, S.4    Garber, J.E.5    Bernhardt, B.6
  • 40
    • 10744233204 scopus 로고    scopus 로고
    • EMSY links the BRCA2 pathway to sporadic breast and ovarian cancer
    • L. Hughes-Davies, D. Huntsman, M. Ruas, F. Fuks, J. Bye, and S.F. Chin EMSY links the BRCA2 pathway to sporadic breast and ovarian cancer Cell 115 2003 523 535
    • (2003) Cell , vol.115 , pp. 523-535
    • Hughes-Davies, L.1    Huntsman, D.2    Ruas, M.3    Fuks, F.4    Bye, J.5    Chin, S.F.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.