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Sci Rep. 2017 Feb 17;7:41921. doi: 10.1038/srep41921.

Palindromic amplification of the ERBB2 oncogene in primary HER2-positive breast tumors.

Author information

1
Lerner Research Institute and Cleveland Clinic, Cleveland, OH, USA.
2
Institute of Medical Science, University of Tokyo, Tokyo, Japan.
3
Department of Surgery, Cedars-Sinai Medical Center, West Hollywood, CA, USA.
4
Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH, USA.

Abstract

Oncogene amplification confers a growth advantage to tumor cells for clonal expansion. There are several, recurrently amplified oncogenes throughout the human genome. However, it remains unclear whether this recurrent amplification is solely a manifestation of increased fitness resulting from random amplification mechanisms, or if a genomic locus-specific amplification mechanism plays a role. Here we show that the ERBB2 oncogene at 17q12 is susceptible to palindromic gene amplification, a mechanism characterized by the inverted (palindromic) duplication of genomic segments, in HER2-positive breast tumors. We applied two genomic approaches to investigate amplification mechanisms: sequencing of DNA libraries enriched with tumor-derived palindromic DNA (Genome-wide Analysis of Palindrome Formation) and whole genome sequencing (WGS). We observed significant enrichment of palindromic DNA within amplified ERBB2 genomic segments. Palindromic DNA was particularly enriched at amplification peaks and at boundaries between amplified and normal copy-number regions. Thus, palindromic gene amplification shaped the amplified ERBB2 locus. The enrichment of palindromic DNA throughout the amplified segments leads us to propose that the ERBB2 locus is amplified through the mechanism that repeatedly generates palindromic DNA, such as Breakage-Fusion-Bridge cycles. The genomic architecture surrounding ERBB2 in the normal genome, such as segmental duplications, could promote the locus-specific mechanism.

PMID:
28211519
PMCID:
PMC5314454
DOI:
10.1038/srep41921
[Indexed for MEDLINE]
Free PMC Article

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