Wooster R, Neuhausen S L, Mangion J, Quirk Y, Ford D, Collins N, Nguyen K, Seal S, Tran T, Averill D
Section of Molecular Carcinogenesis, Institute of Cancer Research, Sutton, Surrey, UK.
Science. 1994 Sep 30;265(5181):2088-90. doi: 10.1126/science.8091231.
A small proportion of breast cancer, in particular those cases arising at a young age, is due to the inheritance of dominant susceptibility genes conferring a high risk of the disease. A genomic linkage search was performed with 15 high-risk breast cancer families that were unlinked to the BRCA1 locus on chromosome 17q21. This analysis localized a second breast cancer susceptibility locus, BRCA2, to a 6-centimorgan interval on chromosome 13q12-13. Preliminary evidence suggests that BRCA2 confers a high risk of breast cancer but, unlike BRCA1, does not confer a substantially elevated risk of ovarian cancer.
一小部分乳腺癌,尤其是那些在年轻时发病的病例,是由于显性易感基因的遗传导致的,这些基因会使人患该病的风险很高。对15个与17号染色体q21位置上的BRCA1基因座没有连锁关系的高危乳腺癌家族进行了基因组连锁搜索。该分析将第二个乳腺癌易感基因座BRCA2定位到13号染色体q12 - 13区域的一个6厘摩区间。初步证据表明,BRCA2会使人患乳腺癌的风险很高,但与BRCA1不同的是,它不会使人患卵巢癌的风险大幅升高。