THE GENETICS OF BREAST AND OVARIAN-CANCER

被引:204
作者
FORD, D
EASTON, DF
机构
[1] Section of Epidemiology, Institute of Cancer Research, Belmont, Surrey, Block D
基金
英国医学研究理事会;
关键词
BREAST CANCER; OVARIAN CANCER; INHERITED PREDISPOSITION; BRCA1; BRCA2; TP53;
D O I
10.1038/bjc.1995.417
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A number of genes are known to be involved in inherited susceptibility to breast and/or ovarian cancer. In the context of high-risk families the most important genes are BRCA1 on chromosome 17q, which is associated with a high penetrance of both breast and ovarian cancer, and BRCA2 on chromosome 13q, which causes a high risk of breast cancer but a lower risk of ovarian cancer. Other high-risk cancer genes that confer increased risks of breast or ovarian cancer in addition to other cancers include the hereditary non-polyposis colorectal cancer genes and the TP53 gene, which causes breast cancer as part of the Li-Fraumeni syndrome. The predisposing mutations in these genes are relatively rare in the population. More common genes which are associated with an increased, but lower, risk of breast cancer are the ataxia-telangiectasia gene and the HRAS1 gene. This paper reviews recent progress in mapping and cloning of these susceptibility genes, and provides estimates of the cancer risks associated with each gene and the frequency of predisposing mutations.
引用
收藏
页码:805 / 812
页数:8
相关论文
共 68 条
  • [1] AALTONEN LA, 1994, CANCER DETECT PREV, V18, P57
  • [2] SEGREGATION AND LINKAGE ANALYSIS OF 9 UTAH BREAST-CANCER PEDIGREES
    BISHOP, DT
    CANNONALBRIGHT, L
    MCLELLAN, T
    GARDNER, EJ
    SKOLNICK, MH
    [J]. GENETIC EPIDEMIOLOGY, 1988, 5 (03) : 151 - 169
  • [3] GENETIC STEPS IN COLORECTAL-CANCER
    BODMER, W
    BISHOP, T
    KARRAN, P
    [J]. NATURE GENETICS, 1994, 6 (03) : 217 - 219
  • [4] BORRESEN AL, 1992, CANCER RES, V52, P3234
  • [5] BREAST-CANCER AND OTHER CANCERS IN NORWEGIAN FAMILIES WITH ATAXIA-TELANGIECTASIA
    BORRESEN, AL
    ANDERSEN, TI
    TRETLI, S
    HEIBERG, A
    MOLLER, P
    [J]. GENES CHROMOSOMES & CANCER, 1990, 2 (04) : 339 - 340
  • [6] BROCA PP, 1866, TRAITES TUMEURS, V1, P80
  • [7] MUTATION IN THE DNA MISMATCH REPAIR GENE HOMOLOG HMLH1 IS ASSOCIATED WITH HEREDITARY NONPOLYPOSIS COLON-CANCER
    BRONNER, CE
    BAKER, SM
    MORRISON, PT
    WARREN, G
    SMITH, LG
    LESCOE, MK
    KANE, M
    EARABINO, C
    LIPFORD, J
    LINDBLOM, A
    TANNERGARD, P
    BOLLAG, RJ
    GODWIN, AR
    WARD, DC
    NORDENSKJOLD, M
    FISHEL, R
    KOLODNER, R
    LISKAY, RM
    [J]. NATURE, 1994, 368 (6468) : 258 - 261
  • [8] COMPLETE NUCLEOTIDE-SEQUENCES OF THE T24 HUMAN BLADDER-CARCINOMA ONCOGENE AND ITS NORMAL HOMOLOG
    CAPON, DJ
    CHEN, EY
    LEVINSON, AD
    SEEBURG, PH
    GOEDDEL, DV
    [J]. NATURE, 1983, 302 (5903) : 33 - 37
  • [9] ORAL-CONTRACEPTIVE USE AND BREAST-CANCER RISK IN YOUNG-WOMEN - SUBGROUP ANALYSES
    CHILVERS, CED
    [J]. LANCET, 1990, 335 (8704) : 1507 - 1509
  • [10] USING AGE OF ONSET TO DISTINGUISH BETWEEN SUBFORMS OF BREAST-CANCER
    CLAUS, EB
    RISCH, NJ
    THOMPSON, WD
    [J]. ANNALS OF HUMAN GENETICS, 1990, 54 : 169 - 177