Evaluation of c-MYC status in primary acquired cholesteatoma by using fluorescence in situ hybridization technique

Otol Neurotol. 2006 Aug;27(5):588-91. doi: 10.1097/01.mao.0000226290.04048.d9.

Abstract

Objective: The object of study was to investigate the status of c-MYC oncogene in primary acquired cholesteatoma.

Study design: Descriptive study.

Methods: Cholesteatoma samples were obtained from 15 patients with primary acquired cholesteatoma during surgical operation. Fluorescence in situ hybridization with a mixed DNA probe, which is specific for c-MYC located on 8q24 and chromosome 8 specific-alpha-satellite DNA probe (dual color), was used on the interphase nuclei.

Results: Copy number of c-MYC oncogene and aneuploidy of chromosome 8 were 21.2% +/- 14.4% and 21.7% +/- 14.8%, respectively. There was no significant difference between copy number of c-MYC and frequency of chromosome 8 aneuploidy (p > 0.05). Ten of 15 cases showed different percentage of c-MYC and chromosome 8 aneuploidy, whereas 5 (33.3%) of 15 cases showed a normal distribution of c-MYC and chromosome 8 signals.

Conclusion: The copy number of c-MYC in 10 of 15 cases was found to be high as observed for chromosome 8 aneuploidy in primary acquired cholesteatoma. These findings suggest that the ability of hyperproliferation of primary acquired cholesteatoma might have been related to c-MYC copy number by deregulating c-MYC expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aneuploidy
  • Cholesteatoma, Middle Ear / genetics*
  • Cholesteatoma, Middle Ear / pathology
  • Chromosomes, Human, Pair 8*
  • DNA-Binding Proteins / analysis*
  • Female
  • Genes, myc*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Interphase
  • Male
  • Middle Aged
  • Transcription Factors / analysis*

Substances

  • DNA-Binding Proteins
  • MYCBP protein, human
  • Transcription Factors