Abstract
Tumours from four individuals in a breast and ovarian cancer family with a known deleterious germline BRCA1 mutation, were analyzed using BRCA1 antibodies. In addition, we examined tumours from 96 female patients with early-onset breast cancer, who were not selected because of any family history. Paraffin-embedded tumour sections were examined by standard immunohistochemical analysis. Three familial tumours from BRCA1 carriers displayed focal negativity. This observation was not seen in a non-mutation carrier from the same family. It was found that 9/96 (9%) early-onset breast tumours had total BRCA1 negativity. In addition, 2/2 (100%) medullary breast carcinomas displayed negativity for both antibodies. Our results indicate that BRCA1 antibodies can discriminate between familial tumours with and without a deleterious mutation from one family. Further mutation studies in early-onset breast cancer group will be necessary to evaluate the use of immunohistochemistry as a rapid, initial screening technique to identify BRCA1 mutations. (C) 2000 Harcourt Publishers Ltd.
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CITATION STYLE
Schofied, A. C., Payne, S., Ross, V. G., Miller, I. D., Heys, S. D., & Haites, N. E. (2000). Immunohistochemical detection of a germline BRCA1 mutation in a breast and ovarian cancer family. Breast, 9(5), 286–291. https://doi.org/10.1054/brst.1999.0090
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