Immunohistochemical detection of a germline BRCA1 mutation in a breast and ovarian cancer family

4Citations
Citations of this article
11Readers
Mendeley users who have this article in their library.
Get full text

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free