Classifications within molecular subtypes enables identification of BRCA1/BRCA2 mutation carriers by RNA tumor profiling

PLoS One. 2013 May 21;8(5):e64268. doi: 10.1371/journal.pone.0064268. Print 2013.

Abstract

Pathogenic germline mutations in BRCA1 or BRCA2 are detected in less than one third of families with a strong history of breast cancer. It is therefore expected that mutations still remain undetected by currently used screening methods. In addition, a growing number of BRCA1/2 sequence variants of unclear pathogen significance are found in the families, constituting an increasing clinical challenge. New methods are therefore needed to improve the detection rate and aid the interpretation of the clinically uncertain variants. In this study we analyzed a series of 33 BRCA1, 22 BRCA2, and 128 sporadic tumors by RNA profiling to investigate the classification potential of RNA profiles to predict BRCA1/2 mutation status. We found that breast tumors from BRCA1 and BRCA2 mutation carriers display characteristic RNA expression patterns, allowing them to be distinguished from sporadic tumors. The majority of BRCA1 tumors were basal-like while BRCA2 tumors were mainly luminal B. Using RNA profiles, we were able to distinguish BRCA1 tumors from sporadic tumors among basal-like tumors with 83% accuracy and BRCA2 from sporadic tumors among luminal B tumors with 89% accuracy. Furthermore, subtype-specific BRCA1/2 gene signatures were successfully validated in two independent data sets with high accuracies. Although additional validation studies are required, indication of BRCA1/2 involvement ("BRCAness") by RNA profiling could potentially be valuable as a tool for distinguishing pathogenic mutations from benign variants, for identification of undetected mutation carriers, and for selecting patients sensitive to new therapeutics such as PARP inhibitors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • BRCA1 Protein / genetics*
  • BRCA2 Protein / genetics*
  • Breast Neoplasms / classification*
  • Breast Neoplasms / genetics*
  • Breast Neoplasms / pathology
  • Cluster Analysis
  • Female
  • Gene Expression Profiling*
  • Gene Expression Regulation, Neoplastic
  • Heterozygote
  • Humans
  • Middle Aged
  • Mutation / genetics*
  • RNA, Neoplasm / genetics*
  • RNA, Neoplasm / metabolism
  • Reproducibility of Results

Substances

  • BRCA1 Protein
  • BRCA2 Protein
  • RNA, Neoplasm

Grants and funding

The work was supported by Heidi Seide Jacobsen, Ministry of the Interior and Ministry of Health, University of Southern Denmark, Odense University Hospital, Danish Cancer Society, The Danish Council for Strategic Research (DBCG-TIBCAT), Dansk Kræftforsknings Fond, Breast Friends, Københavns Universitets fond for kræftforskning, Savværksejer Jeppe Juhls og hustru Ovita Juhls Mindelegat, Arvid Nilssons Fond, Agnes og Poul Friis Fond, Raimond og Dagmar Ringgård Bohns Fond, Fonden til Lægevidenskabens Fremme, Kong Christian IX og Dronning Louises Jubilæumslegat, Ingeniør K. A. Rohde og hustrus Legat, Snedkermester Sophus Jacobsens og hustru Astrid Jacobsens Fond, Fru Astrid Thaysens Legat for Lægevidenskabelig Grundforskning, Helen Rudes Fond, Karen A. Tolstrups Fond. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.