GRCh38 · COSMIC v99


This section shows a summary for the selected study (COSU identifier) or publication (COSP identifier). Studies may have been performed by the Sanger Institute Cancer Genome Project, or imported from the ICGC/TCGA. You can see more information on the help pages.

Whole-Exome and RNA-Sequencing Analyses of Acinic Cell Carcinomas of the Breast.
Paper ID
Beca F, Lee SSK, Pareja F, da Cruz Paula A, Selenica P, Ferrando L, Gularte-Merida R, Wen HY, Zhang H, Guerini-Rocco E, Rakha EA, Weigelt B and Reis-Filho JS
Department of Pathology, Stanford School of Medicine, Stanford, CA, USA.
Histopathology, 2019
ISSN: 1365-2559
PMID: 31361912 (view at PubMed or Europe PMC)
Aims: Acinic cell carcinoma of the breast (ACC) is a rare histologic form of triple-negative breast cancer (TNBC). Despite its unique histology, targeted sequencing analysis has failed to identify recurrent genetic alterations other than those found in common forms of TNBC. Here, we subjected three breast ACCs to whole-exome and RNA-sequencing, seeking to define whether they would harbor a pathognomonic genetic alteration.Tumor and normal DNA and RNA samples from three breast ACCs were subjected to whole-exome sequencing. Somatic mutations, copy number alterations, mutational signatures and fusion genes were determined using state-of-the-art bioinformatics methods. Our analyses revealed TP53 hotspot mutations associated with loss of heterozygosity of the wild-type allele in two cases. Mutations affecting homologous recombination (HR) DNA repair-related genes were found in two cases, and an MLH1 pathogenic germline variant was detected in one case. In addition, copy number analysis revealed the presence of a somatic BRCA1 homozygous deletion and focal amplification of 12q14.3-12q21.1, encompassing MDM2, HMGA2, FRS2 and PTPRB. No oncogenic in-frame fusion transcript was identified in the three breast ACCs analyzed.Conclusions: No pathognomonic genetic alterations were detected in the ACCs analyzed. These tumors have somatic genetic alterations similar to those of common forms of TNBC and may display HR deficiency or microsatellite instability. These findings provide further insights as to why ACCs which are usually clinically indolent may evolve into or in parallel with high-grade TNBC. This article is protected by copyright. All rights reserved.
Paper Status