A subset of pancreatic adenocarcinomas demonstrates coamplification of topoisomerase IIα and HER2/neu: Use of immunolabeling and multicolor FISH for potential patient screening and treatment

Donna E. Hansel, Raheela Ashfaq, Ayman Rahman, Dana Wanzer, Charles J. Yeo, Robb E. Wilentz, Anirban Maitra

Research output: Contribution to journalArticle

Abstract

We sought to identify the frequency of amplification of the topoisomerase IIα gene (TOP2A) in pancreatic cancer and determine the usefulness of TOP2A immunolabeling in screening for TOP2A and human epidermal growth factor receptor (HER)2/neu amplification. We examined 55 pancreatic adenocarcinoma specimens for TOP2A immunolabeling and identified TOP2A protein expression in all specimens with a nuclear labeling index (NLI; positive nuclei/total nuclei × 100) of 5% to 80%. Normal pancreatic ductal epithelium, proposed to give rise to pancreatic adenocarcinoma, did not demonstrate detectable TOP2A expression. In a subset of specimens selected for fluorescence in situ hybridization analysis of TOP2A and HER2/neu amplification using a recently developed multicolor probe, 7 of 8 lesions with an NLI of 25% or more demonstrated TOP2A amplification, in contrast with 2 of 14 lesions with a TOP2A NLI of less than 25%. In 8 of 9 TOP2A-amplified cases, coamplification of HER2/neu was present, suggesting a potential relationship between TOP2A and HER2/neu in pancreatic adenocarcinoma. We propose that TOP2A immunolabeling be used in conjunction with a newly developed multicolor probe to screen patients with pancreatic adenocarcinoma to determine the best potential therapeutic modalities, such as TOP2A inhibitors, trastuzumab, or both.

Original languageEnglish (US)
Pages (from-to)28-35
Number of pages8
JournalAmerican Journal of Clinical Pathology
Volume123
Issue number1
DOIs
StatePublished - Jan 2005

Keywords

  • Cancer
  • FISH
  • Fluorescence in situ hybridization
  • Immunolabeling
  • Pancreas
  • Screening

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

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