The pathology of familial breast cancer:: Predictive value of immunohistochemical markers estrogen receptor, progesterone receptor, HER-2, and p53 in patients with mutations in BRCA1 and BRCA2

被引:636
作者
Lakhani, SR
van de Vijver, MJ
Jacquemier, J
Anderson, TJ
Osin, PP
McGuffog, L
Easton, DF
机构
[1] Inst Canc Res, Breakthrough Toby Robins Breast Canc Res Ctr, Chester Beatty Labs, London SW3 6JB, England
[2] Royal Marsden Hosp, London SW3 6JJ, England
[3] UCL Royal Free & Univ Coll Med Sch, Dept Histopathol, London, England
[4] Univ Edinburgh, Sch Med, Dept Pathol, Edinburgh, Midlothian, Scotland
[5] CRC, Genet Epidemiol Unit, Strangeways Res Lab, Cambridge, England
[6] Netherlands Canc Inst, Antoni Van Leeuwenhoek Huis, Amsterdam, Netherlands
[7] Inst J Paoli I Calmettes, Dept Genet Oncol & Canc Control, F-13009 Marseille, France
关键词
D O I
10.1200/JCO.2002.09.023
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose : The morphologic and molecular phenotype of breast cancers may help identify patients who are likely to carry germline mutations in BRCA1 and BRCA2. This study evaluates the immunohistochemical profiles of tumors arising in patients with mutations in these genes. Materials and Methods: Samples of breast cancers obtained from the International Breast Cancer Linkage Consortium were characterized morphologically and immunohistochemically using antibodies to estrogen receptor, progesterone receptor, HER-2 (c-erbB-2 oncogene), and p53 protein. Results: Breast cancers in patients with BRCA1 germline mutations are more often negative for estrogen receptor, progesterone receptor, and HER-2, and are more likely to be positive for p53 protein compared with controls. In contrast, BRCA2 tumors do not show a significant difference in the expression of any of these proteins compared with controls. Conclusion: BRCA1 has a distinctive morphology and immunohistochemical phenotype. The combined morphologic and immunohistochemical data can be used to predict the risk of a young patient harboring a germline mutation in BRCA1. The BRCA2 phenotype is currently not well defined. (C) 2002 by American Society of Clinical Oncology.
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页码:2310 / 2318
页数:9
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