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Volumn 86, Issue 8 SUPPL., 1999, Pages 1673-1681

Inherited genetic predisposition in breast cancer: A population-based perspective

Author keywords

Breast cancer; Inherited susceptibility; Major gene; Polygene

Indexed keywords

BREAST CANCER; CANCER GENETICS; CANCER PREVENTION; CANCER RISK; CONFERENCE PAPER; GENETIC EPIDEMIOLOGY; GENETIC PREDISPOSITION; GENETIC RISK; GENETIC SUSCEPTIBILITY; HUMAN; ONCOGENE; PEDIGREE; PRIORITY JOURNAL; RISK ASSESSMENT;

EID: 0033569803     PISSN: 0008543X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1097-0142(19991015)86:8+<1673::aid-cncr6>3.0.co;2-b     Document Type: Conference Paper
Times cited : (20)

References (58)
  • 2
    • 0027433563 scopus 로고
    • Genetic linkage analysis in familial breast and ovarian cancer: Results from 214 families
    • Easton DF, Bishop DT, Ford D, Crockford GP, and the Breast Cancer Linkage Consortium. Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. Am J Hum Genet 1993;52:678-701
    • (1993) Am J Hum Genet , vol.52 , pp. 678-701
    • Easton, D.F.1    Bishop, D.T.2    Ford, D.3    Crockford, G.P.4
  • 3
    • 0032565070 scopus 로고    scopus 로고
    • Frequency of breast cancer attributable to BRCA1 in a population-based series of American women
    • Newman B, Mu H, Butler LM, Millikan RC, Moorman PG, King MC. Frequency of breast cancer attributable to BRCA1 in a population-based series of American women. JAMA 1998;279:915-21
    • (1998) JAMA , vol.279 , pp. 915-921
    • Newman, B.1    Mu, H.2    Butler, L.M.3    Millikan, R.C.4    Moorman, P.G.5    King, M.C.6
  • 4
    • 0029587042 scopus 로고
    • A tale of four syndromes: Familial adenomatous polyposis, Gardner syndrome, attenuated APC and Turcot syndrome
    • Foulkes WD. A tale of four syndromes: familial adenomatous polyposis, Gardner syndrome, attenuated APC and Turcot syndrome. QJM 1995;88:853-63.
    • (1995) QJM , vol.88 , pp. 853-863
    • Foulkes, W.D.1
  • 8
    • 0016286319 scopus 로고
    • Genetic study of breast cancer: Identification of a high risk group
    • Anderson DE. Genetic study of breast cancer: identification of a high risk group. Cancer 1974;34:1090-7.
    • (1974) Cancer , vol.34 , pp. 1090-1097
    • Anderson, D.E.1
  • 9
    • 0026092912 scopus 로고
    • Genetic analysis of breast cancer in the Cancer and Steroid Hormone Study
    • Claus EB, Risch N, Thompson WD. Genetic analysis of breast cancer in the Cancer and Steroid Hormone Study. Am J Hum Genet 1991;48:232-42.
    • (1991) Am J Hum Genet , vol.48 , pp. 232-242
    • Claus, E.B.1    Risch, N.2    Thompson, W.D.3
  • 11
    • 0028113345 scopus 로고
    • A strong candidate gene for the breast and ovarian cancer susceptibility gene BRCA 1
    • Miki Y, Swensen J, Shattuck-Eidens S, Futreal A, Harshman K, Tavigian S, et al. A strong candidate gene for the breast and ovarian cancer susceptibility gene BRCA 1. Science 1994; 266:66-71.
    • (1994) Science , vol.266 , pp. 66-71
    • Miki, Y.1    Swensen, J.2    Shattuck-Eidens, S.3    Futreal, A.4    Harshman, K.5    Tavigian, S.6
  • 12
    • 0032528265 scopus 로고    scopus 로고
    • Concise handbook of family cancer syndromes
    • Lindor NM, Greene MH, and the Mayo Familial Cancer Program. Concise handbook of family cancer syndromes. J Natl Cancer Inst 1998;90:1039-71.
    • (1998) J Natl Cancer Inst , vol.90 , pp. 1039-1071
    • Lindor, N.M.1    Greene, M.H.2
  • 13
    • 17344365851 scopus 로고    scopus 로고
    • Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in BC families
    • The BC Linkage Consortium
    • Ford D, Easton DF, Stratton M, Narod S, Goldgar D, Devilee P, et al. Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in BC families. The BC Linkage Consortium. Am J Hum Genet 1998;62:676-89.
    • (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
  • 17
    • 0028844202 scopus 로고
    • Germline variants of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype-phenotype correlation
    • Gayther SA, Warren W, Mazoyer S, Russell PA, Harrington PA, Chiano M, et al. Germline variants of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype-phenotype correlation. Nat Genet 1995;11:428-33.
    • (1995) Nat Genet , vol.11 , pp. 428-433
    • Gayther, S.A.1    Warren, W.2    Mazoyer, S.3    Russell, P.A.4    Harrington, P.A.5    Chiano, M.6
  • 18
    • 0031012305 scopus 로고    scopus 로고
    • Variation of risks of breast and ovarian cancer associated with different germline variants of the BRCA2 gene
    • Gayther SA, Mangion J, Russell P, Seal S, Barfoot R, Ponder BA, et al. Variation of risks of breast and ovarian cancer associated with different germline variants of the BRCA2 gene. Nat Genet 1997;15:103-5.
    • (1997) Nat Genet , vol.15 , pp. 103-105
    • Gayther, S.A.1    Mangion, J.2    Russell, P.3    Seal, S.4    Barfoot, R.5    Ponder, B.A.6
  • 19
    • 13344268996 scopus 로고    scopus 로고
    • Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeats (VNTR) locus
    • Phelan CM, Rebbeck TR, Weber BL, Devilee P, Ruttledge MH, Lynch HT, et al. Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeats (VNTR) locus. Nat Genet 1996;12:309-11.
    • (1996) Nat Genet , vol.12 , pp. 309-311
    • Phelan, C.M.1    Rebbeck, T.R.2    Weber, B.L.3    Devilee, P.4    Ruttledge, M.H.5    Lynch, H.T.6
  • 20
    • 0001516492 scopus 로고    scopus 로고
    • Modification of breast cancer risk in BRCA1 variant carriers by the androgen receptor CAG repeat polymorphism
    • Rebbeck TR, Kantoff PW, Krithivas K, Narod SA, Godwin AK, Daly MB, et al. Modification of breast cancer risk in BRCA1 variant carriers by the androgen receptor CAG repeat polymorphism. Am J Hum Genet 1999;64:1371-7.
    • (1999) Am J Hum Genet , vol.64 , pp. 1371-1377
    • Rebbeck, T.R.1    Kantoff, P.W.2    Krithivas, K.3    Narod, S.A.4    Godwin, A.K.5    Daly, M.B.6
  • 22
    • 0030865837 scopus 로고
    • Does oral contraceptive use increase the risk of BC in women with BRCA1/BRCA2 variants more than in other women?
    • Ursin G, Henderson BE, Haue RW, Pike MC, Zhou N, Diep A, et al. Does oral contraceptive use increase the risk of BC in women with BRCA1/BRCA2 variants more than in other women? Cancer Res 1991;57:3678-81.
    • (1991) Cancer Res , vol.57 , pp. 3678-3681
    • Ursin, G.1    Henderson, B.E.2    Haue, R.W.3    Pike, M.C.4    Zhou, N.5    Diep, A.6
  • 26
    • 0028246715 scopus 로고
    • Statistical analysis of molecular epidemiology studies employing case-series
    • Begg CB, Zhang ZF. Statistical analysis of molecular epidemiology studies employing case-series. Cancer Epidemiol Biomarkers Prev 1994;3:173-5.
    • (1994) Cancer Epidemiol Biomarkers Prev , vol.3 , pp. 173-175
    • Begg, C.B.1    Zhang, Z.F.2
  • 27
    • 0028089404 scopus 로고
    • Non-hierarchical logistic models and case-only designs for assessing susceptibility in population-based case-control studies
    • Piegorsch WW, Weinberg CR, Taylor JA. Non-hierarchical logistic models and case-only designs for assessing susceptibility in population-based case-control studies. Stat Med 1994;13:153-62.
    • (1994) Stat Med , vol.13 , pp. 153-162
    • Piegorsch, W.W.1    Weinberg, C.R.2    Taylor, J.A.3
  • 28
    • 0000575788 scopus 로고
    • Genetics of HLA disease associations: The use of the haplotype relative risk (HRR) and the "haplo-delta" (Dh) estimates in juvenile diabetes from three racial groups
    • Rubinstein P, Walker M, Carpenter C, Carrier C, Krassner J, Falk C, et al. Genetics of HLA disease associations: the use of the haplotype relative risk (HRR) and the "haplo-delta" (Dh) estimates in juvenile diabetes from three racial groups. Hum Immunol 1981;3:384-8.
    • (1981) Hum Immunol , vol.3 , pp. 384-388
    • Rubinstein, P.1    Walker, M.2    Carpenter, C.3    Carrier, C.4    Krassner, J.5    Falk, C.6
  • 29
    • 0027377799 scopus 로고
    • Transmission disequilibrium test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
    • Spielman RS, McGinnis RE, Ewens WJ. Transmission disequilibrium test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet 1993;52:506-16.
    • (1993) Am J Hum Genet , vol.52 , pp. 506-516
    • Spielman, R.S.1    McGinnis, R.E.2    Ewens, W.J.3
  • 32
    • 0023244806 scopus 로고
    • Breast and other cancers in families with ataxia-telangiectasia
    • Swift M, Reitnauer PJ, Morrell D, Chase CL. Breast and other cancers in families with ataxia-telangiectasia. N Engl J Medicine 1987;316:1289-94.
    • (1987) N Engl J Medicine , vol.316 , pp. 1289-1294
    • Swift, M.1    Reitnauer, P.J.2    Morrell, D.3    Chase, C.L.4
  • 35
    • 9344219890 scopus 로고    scopus 로고
    • The ATM gene and susceptibility to BC: Analysis of 38 breast tumors reveals no evidence for variant
    • Vorechovsky I, Rasio D, Luo L, Monaco C, Hammarstrom L, Webster AD, et al. The ATM gene and susceptibility to BC: analysis of 38 breast tumors reveals no evidence for variant. Cancer Res 1996;56:2726-32.
    • (1996) Cancer Res , vol.56 , pp. 2726-2732
    • Vorechovsky, I.1    Rasio, D.2    Luo, L.3    Monaco, C.4    Hammarstrom, L.5    Webster, A.D.6
  • 36
    • 8044220285 scopus 로고    scopus 로고
    • Recommendations for follow-up care of individuals with an inherited predisposition to cancer. I. Hereditary nonpolyposis colon cancer
    • Cancer Genetics Studies Consortium
    • Burke W, Petersen G, Lynch P, Botkin J, Daly M, Garber J, et al. Recommendations for follow-up care of individuals with an inherited predisposition to cancer. I. Hereditary nonpolyposis colon cancer. Cancer Genetics Studies Consortium. JAMA 1997;277:915-9.
    • (1997) JAMA , vol.277 , pp. 915-919
    • Burke, W.1    Petersen, G.2    Lynch, P.3    Botkin, J.4    Daly, M.5    Garber, J.6
  • 37
    • 0030910022 scopus 로고    scopus 로고
    • The risk of cancer associated with specific variants of BRCA1 and BRCA2 among Ashkenazi Jews
    • Struewing JP, Hartge P, Wacholder S, Baker SM, Berlin M, McAdams M, et al. The risk of cancer associated with specific variants of BRCA1 and BRCA2 among Ashkenazi Jews. N Engl J Med 1997;336:1401-8.
    • (1997) N Engl J Med , vol.336 , pp. 1401-1408
    • Struewing, J.P.1    Hartge, P.2    Wacholder, S.3    Baker, S.M.4    Berlin, M.5    McAdams, M.6
  • 38
    • 0025633582 scopus 로고
    • Germ line p53 variants in a familial syndrome of BC, sarcomas, and other neoplasms
    • Malkin D, Li FP, Strong LC, Fraumeni JF Jr, Nelson CE, Kim DH, et al. Germ line p53 variants in a familial syndrome of BC, sarcomas, and other neoplasms. Science 1990;250:1233-8.
    • (1990) Science , vol.250 , pp. 1233-1238
    • Malkin, D.1    Li, F.P.2    Strong, L.C.3    Fraumeni J.F., Jr.4    Nelson, C.E.5    Kim, D.H.6
  • 40
    • 0028220688 scopus 로고
    • Prevalence and diversity of constitutional variants in the p53 gene among 21 Li-Fraumeni families
    • Birch JM, Hartley AL, Ticker KJ. Prevalence and diversity of constitutional variants in the p53 gene among 21 Li-Fraumeni families. Cancer Res 1994;54:1298-1304.
    • (1994) Cancer Res , vol.54 , pp. 1298-1304
    • Birch, J.M.1    Hartley, A.L.2    Ticker, K.J.3
  • 41
    • 0018140493 scopus 로고
    • Cowden's disease: A cutaneous marker of BC
    • Brownstein MH, Wolf M, Bikowski JB. Cowden's disease: a cutaneous marker of BC. Cancer 1978 41:2393-8.
    • (1978) Cancer , vol.41 , pp. 2393-2398
    • Brownstein, M.H.1    Wolf, M.2    Bikowski, J.B.3
  • 42
    • 0030936323 scopus 로고    scopus 로고
    • PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer
    • Li J, Yen C, Liaw D, Podsypanina K, Bose S, Wang SI, et al. PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer. Science 1997;275:1943-7.
    • (1997) Science , vol.275 , pp. 1943-1947
    • Li, J.1    Yen, C.2    Liaw, D.3    Podsypanina, K.4    Bose, S.5    Wang, S.I.6
  • 44
    • 0031974516 scopus 로고    scopus 로고
    • Peutz-Jeghers syndrome is caused by variants in a novel serine threonine kinase
    • Jenne DE, Reimann H, Nezu J, Friedel W, Loff S, Jeschke R, et al. Peutz-Jeghers syndrome is caused by variants in a novel serine threonine kinase. Nat Genet 1998;18:38-43.
    • (1998) Nat Genet , vol.18 , pp. 38-43
    • Jenne, D.E.1    Reimann, H.2    Nezu, J.3    Friedel, W.4    Loff, S.5    Jeschke, R.6
  • 46
    • 0031984229 scopus 로고    scopus 로고
    • BC and CYPIA1, GSTM1, and GSTT1 polymorphisms: Evidence of a lack of association in Caucasians and African Americans
    • Bailey LR, Roodi N, Verrier CS, Yee CJ, Dupont WD, Pari FF. BC and CYPIA1, GSTM1, and GSTT1 polymorphisms: evidence of a lack of association in Caucasians and African Americans. Cancer Res 1998;58:65-70.
    • (1998) Cancer Res , vol.58 , pp. 65-70
    • Bailey, L.R.1    Roodi, N.2    Verrier, C.S.3    Yee, C.J.4    Dupont, W.D.5    Pari, F.F.6
  • 47
    • 0029813002 scopus 로고    scopus 로고
    • Lack of a relationship between the debrisoquine (CYP2D6) and mephenytoin (CYP2C19) oxidation polymorphisms and susceptibility to breast cancer
    • Jennings M, Sweetand H, Smith CAD, Wolf CR, Lennard MS, Tucker GT, et al. Lack of a relationship between the debrisoquine (CYP2D6) and mephenytoin (CYP2C19) oxidation polymorphisms and susceptibility to breast cancer. Breast 1996;5:254-8.
    • (1996) Breast , vol.5 , pp. 254-258
    • Jennings, M.1    Sweetand, H.2    Smith, C.A.D.3    Wolf, C.R.4    Lennard, M.S.5    Tucker, G.T.6
  • 50
    • 0032054961 scopus 로고    scopus 로고
    • Association between glutathione S-transferase M1, P1, and T1 genetic polymorphisms and development of BC
    • Helzlsouer KJ, Selmin O, Huang HY. Association between glutathione S-transferase M1, P1, and T1 genetic polymorphisms and development of BC. J Natl Cancer Inst 1998;90: 512-8.
    • (1998) J Natl Cancer Inst , vol.90 , pp. 512-518
    • Helzlsouer, K.J.1    Selmin, O.2    Huang, H.Y.3
  • 51
    • 17344390987 scopus 로고    scopus 로고
    • Allelic deletion at glutathione S-transferase M1 focus and its association with BC susceptibility
    • Maugard CM, Charrier J, Bignon YJ. Allelic deletion at glutathione S-transferase M1 focus and its association with BC susceptibility. Chem Biol Interact 1998;112:365-75.
    • (1998) Chem Biol Interact , vol.112 , pp. 365-375
    • Maugard, C.M.1    Charrier, J.2    Bignon, Y.J.3
  • 52
    • 0027214689 scopus 로고
    • An association between the risk of cancer and variants in the HRAS1 minisatellite locus
    • Krontiris TG, Devlin B, Karp DD, Robert NJ, Risch N. An association between the risk of cancer and variants in the HRAS1 minisatellite locus. N Engl J Med 1993;329:517-23.
    • (1993) N Engl J Med , vol.329 , pp. 517-523
    • Krontiris, T.G.1    Devlin, B.2    Karp, D.D.3    Robert, N.J.4    Risch, N.5
  • 55
    • 0032514413 scopus 로고    scopus 로고
    • Oral contraceptives and the risk of hereditary ovarian cancer
    • Hereditary Ovarian Cancer Clinical Study Group
    • Narod SA, Risch H, Moslehi R, Dorum A, Neuhausen S, Olsson H, et al. Oral contraceptives and the risk of hereditary ovarian cancer. Hereditary Ovarian Cancer Clinical Study Group. New Engl Journ Med 1998;339:424-8.
    • (1998) New Engl Journ Med , vol.339 , pp. 424-428
    • Narod, S.A.1    Risch, H.2    Moslehi, R.3    Dorum, A.4    Neuhausen, S.5    Olsson, H.6
  • 56
    • 14444276295 scopus 로고    scopus 로고
    • Genetic polymorphisms in catechol-O-methyltransferase, menopausal status, and breast cancer risk
    • Thompson PA, Shields PG, Freudenheim JL, Stone A, Vena JE, Marshall JR, et al. Genetic polymorphisms in catechol-O-methyltransferase, menopausal status, and breast cancer risk. Cancer Res 1998;58:2107-10.
    • (1998) Cancer Res , vol.58 , pp. 2107-2110
    • Thompson, P.A.1    Shields, P.G.2    Freudenheim, J.L.3    Stone, A.4    Vena, J.E.5    Marshall, J.R.6
  • 57
    • 15144339383 scopus 로고    scopus 로고
    • An association between the allele coding for a low activity variant of catechol-O-methyltransferase and the risk for breast cancer
    • Lavigne JA, Helzlsouer KJ, Huang HY, Strickland PT, Bell DA, Selmin O, et al. An association between the allele coding for a low activity variant of catechol-O-methyltransferase and the risk for breast cancer. Cancer Res. 1997;57:5493-7.
    • (1997) Cancer Res. , vol.57 , pp. 5493-5497
    • Lavigne, J.A.1    Helzlsouer, K.J.2    Huang, H.Y.3    Strickland, P.T.4    Bell, D.A.5    Selmin, O.6


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