Systems consequences of amplicon formation in human breast cancer

Genome Res. 2014 Oct;24(10):1559-71. doi: 10.1101/gr.164871.113. Epub 2014 Sep 3.

Abstract

Chromosomal structural variations play an important role in determining the transcriptional landscape of human breast cancers. To assess the nature of these structural variations, we analyzed eight breast tumor samples with a focus on regions of gene amplification using mate-pair sequencing of long-insert genomic DNA with matched transcriptome profiling. We found that tandem duplications appear to be early events in tumor evolution, especially in the genesis of amplicons. In a detailed reconstruction of events on chromosome 17, we found large unpaired inversions and deletions connect a tandemly duplicated ERBB2 with neighboring 17q21.3 amplicons while simultaneously deleting the intervening BRCA1 tumor suppressor locus. This series of events appeared to be unusually common when examined in larger genomic data sets of breast cancers albeit using approaches with lesser resolution. Using siRNAs in breast cancer cell lines, we showed that the 17q21.3 amplicon harbored a significant number of weak oncogenes that appeared consistently coamplified in primary tumors. Down-regulation of BRCA1 expression augmented the cell proliferation in ERBB2-transfected human normal mammary epithelial cells. Coamplification of other functionally tested oncogenic elements in other breast tumors examined, such as RIPK2 and MYC on chromosome 8, also parallel these findings. Our analyses suggest that structural variations efficiently orchestrate the gain and loss of cancer gene cassettes that engage many oncogenic pathways simultaneously and that such oncogenic cassettes are favored during the evolution of a cancer.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • BRCA1 Protein / genetics*
  • Base Sequence
  • Breast Neoplasms / genetics*
  • Cell Line, Tumor
  • Chromosome Aberrations*
  • Chromosomes, Human, Pair 17 / genetics*
  • Female
  • Gene Amplification
  • Gene Duplication
  • Gene Expression Profiling
  • Gene Expression Regulation, Neoplastic
  • Humans
  • MCF-7 Cells
  • Molecular Sequence Data
  • Receptor, ErbB-2 / genetics*
  • Sequence Analysis, DNA

Substances

  • BRCA1 Protein
  • BRCA1 protein, human
  • ERBB2 protein, human
  • Receptor, ErbB-2

Associated data

  • GEO/GSE57914
  • SRA/PRJNA251354
  • SRA/PRJNA253369