Tonin P, Moslehi R, Green R, Rosen B, Cole D, Boyd N, Cutler C, Margolese R, Carter R, McGillivray B
Department of Medicine, McGill University, Montreal, Quebec, Canada.
Hum Genet. 1995 May;95(5):545-50. doi: 10.1007/BF00223867.
We have examined 26 Canadian families with hereditary breast or ovarian cancer for linkage to markers flanking the BRCA1 gene on chromosome 17q12-q21. Of the 15 families that contain cases of ovarian cancer, 94% were estimated to be linked to BRCA1. In contrast, there was no overall evidence of linkage in the group of 10 families with breast cancer without ovarian cancer. A genetic recombinant in a breast-ovarian cancer family indicates a placement of BRCA1 telomeric to D17S776, and helps to define the region of assignment of the cancer susceptibility gene. Other cancers of interest that appeared in the BRCA1-linked families included primary peritoneal cancer, cancer of the fallopian tube, and malignant melanoma.
我们研究了26个患有遗传性乳腺癌或卵巢癌的加拿大家庭,以确定其与位于17号染色体q12 - q21区域的BRCA1基因侧翼标记的连锁关系。在15个包含卵巢癌病例的家庭中,估计94%与BRCA1连锁。相比之下,在10个无卵巢癌的乳腺癌家庭组中,没有整体的连锁证据。一个乳腺癌 - 卵巢癌家庭中的基因重组表明BRCA1位于D17S776的端粒侧,并有助于确定癌症易感基因的定位区域。在与BRCA1连锁的家庭中出现的其他相关癌症包括原发性腹膜癌、输卵管癌和恶性黑色素瘤。