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PMID: 16687925 Published · ppublish English Journal Article Review

The basal phenotype of BRCA1-related breast cancer: past, present and future.

Cell cycle (Georgetown, Tex.) ·Vol. 5 ·No. 9 ·2006-05-00 ·Pages 963-7

Tischkowitz MD, Foulkes WD

Abstract

Many BRCA1-related tumors have a distinct histological characteristics which together have been called "basal-like." Typically such tumors are ER-, HER2- and express cytokeratin 5/6, cytokeratin 8/18, EGFR and vimentin. These characteristics can be used to predict which breast cancers are most likely to be associated with germline BRCA1 mutations which has important implications for breast pathologists. Moreover, BRCA1-related breast cancers generally have a poorer prognosis which may paradoxically be more pronounced in node negative cancers. This may relate in part to a different pattern of metastatic spread with in increased frequency of brain and lung metastases in BRCA1 carriers. Conversely, BRCA1-related tumors may respond better to neoadjuvant chemotherapy and their characteristic molecular signature may provide opportunities to develop specific molecular targeted therapies akin to traztuzumab in HER2+ cancers. Finally, many of the phenotypic features of BRCA1-related tumors might also be found in putative breast stem cells and therefore characterization of the BRCA1 breast cancer phenotype will improve our understanding of sporadic breast carcinogenesis.

MeSH Terms
Biomarkers, Tumor Breast Neoplasms/genetics,pathology,therapy Female Genes, BRCA1 Humans Mutation Neoplastic Stem Cells/pathology Phenotype Prognosis
Chemicals
Biomarkers, Tumor
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Tischkowitz Marc D
Cancer Prevention Centre, Sir M.B. Davis Jewish General Hospital, McGill University, Montreal, QC, Canada. marc.tischkowitz@mcgill.ca
Foulkes William D
Article Info
Journal
Cell cycle (Georgetown, Tex.)
Abbr.
Cell Cycle
ISSN
1551-4005
Published
2006-05-00
Epub
2006-00-01
Pages
963-7
Language
English
Region
United States
NLM ID
101137841
Subset
IM
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