Metastatic breast carcinomas display genomic and transcriptomic heterogeneity Journal Article


Authors: Weigelt, B.; Ng, C. K. Y.; Shen, R.; Popova, T.; Schizas, M.; Natrajan, R.; Mariani, O.; Stern, M. H.; Norton, L.; Vincent-Salomon, A.; Reis-Filho, J. S.
Article Title: Metastatic breast carcinomas display genomic and transcriptomic heterogeneity
Abstract: Metaplastic breast carcinoma is a rare and aggressive histologic type of breast cancer, preferentially displaying a triple-negative phenotype. We sought to define the transcriptomic heterogeneity of metaplastic breast cancers on the basis of current gene expression microarray-based classifiers, and to determine whether these tumors display gene copy number profiles consistent with those of BRCA1-associated breast cancers. Twenty-eight consecutive triple-negative metaplastic breast carcinomas were reviewed, and the metaplastic component present in each frozen specimen was defined (ie, spindle cell, squamous, chondroid metaplasia). RNA and DNA extracted from frozen sections with tumor cell content >60% were subjected to gene expression (Illumina HumanHT-12 v4) and copy number profiling (Affymetrix SNP 6.0), respectively. Using the best practice PAM50/claudin-low microarray-based classifier, all metaplastic breast carcinomas with spindle cell metaplasia were of claudin-low subtype, whereas those with squamous or chondroid metaplasia were preferentially of basal-like subtype. Triple-negative breast cancer subtyping using a dedicated website (http://cbc.mc.vanderbilt.edu/tnbc/) revealed that all metaplastic breast carcinomas with chondroid metaplasia were of mesenchymal-like subtype, spindle cell carcinomas preferentially of unstable or mesenchymal stem-like subtype, and those with squamous metaplasia were of multiple subtypes. None of the cases was classified as immunomodulatory or luminal androgen receptor subtype. Integrative clustering, combining gene expression and gene copy number data, revealed that metaplastic breast carcinomas with spindle cell and chondroid metaplasia were preferentially classified as of integrative clusters 4 and 9, respectively, whereas those with squamous metaplasia were classified into six different clusters. Eight of the 26 metaplastic breast cancers subjected to SNP6 analysis were classified as BRCA1-like. The diversity of histologic features of metaplastic breast carcinomas is reflected at the transcriptomic level, and an association between molecular subtypes and histology was observed. BRCA1-like genomic profiles were found only in a subset (31%) of metaplastic breast cancers, and were not associated with a specific molecular or histologic subtype. © 2015 USCAP, Inc. All rights reserved.
Keywords: immunohistochemistry; clinical article; human tissue; allele; gene expression; gene expression profiling; gene frequency; brca1 protein; transcriptomics; tumor cell; genomics; androgen receptor; gene dosage; cancer classification; spindle cell carcinoma; genetic heterogeneity; copy number variation; triple negative breast cancer; squamous cell metaplasia; claudin; human; priority journal; article; triple negative metaplastic breast carcinoma
Journal Title: Modern Pathology
Volume: 28
Issue: 3
ISSN: 0893-3952
Publisher: Nature Research  
Date Published: 2015-03-01
Start Page: 340
End Page: 351
Language: English
DOI: 10.1038/modpathol.2014.142
PROVIDER: scopus
PUBMED: 25412848
PMCID: PMC4523239
DOI/URL:
Notes: Export Date: 2 September 2015 -- Source: Scopus
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MSK Authors
  1. Larry Norton
    760 Norton
  2. Ronglai Shen
    206 Shen
  3. Britta Weigelt
    641 Weigelt
  4. Kiu Yan Charlotte Ng
    155 Ng
  5. Michail Schizas
    27 Schizas