Different amplification patterns of the human telomerase RNA gene in invasive cervical carcinomas and cervical intraepithelial neoplasia grade III

Diagn Cytopathol. 2012 Oct;40(10):849-55. doi: 10.1002/dc.21635. Epub 2011 Mar 4.

Abstract

The aim of this study was to compare the amplification patterns of the human telomerase RNA gene (hTERC) in invasive cervical carcinomas (ICC) and cervical intraepithelial neoplasia grade III (CIN III) and to define their potential clinical implications. Cervical liquid-based cytological (LBC) specimens were collected from 53 squamous cell carcinomas (SCC), 14 CIN III, and 20 normal controls. Copy numbers of the hTERC gene were measured by fluorescence in situ hybridization (FISH) using a dual-color probe containing the hTERC probe and the control, chromosome 3 centromere-specific probe (CSP3). Nucleus with abnormal FISH pattern for hTERC was observed in 0.94-90.65% of SCC cells and in 0-85.59% of CIN III cells. Using the threshold of 5.89%, the occurrence of hTERC amplification in SCC and CIN III was similar (90.6% vs. 85.7%, P = 0.630). However, the median percentage of cells with extra gains of hTERC (hTERC:CSP3 > 1) in SCC was higher than in CIN III (64.3% vs. 31.7%, P = 0.001). Among those cells, the 3:2 signal pattern was the leading pattern for both SCC and CIN III; high-level amplification of hTERC was more common in SCC than in CIN III (60.9% vs. 48.9%, P = 0.002). In SCC, it was not found that extra gains of hTERC were associated with any clinicopathological parameters. Thus, hTERC amplification was common in cervical exfoliated cells from SCC and CIN III. More complex amplification patterns of hTERC were present in ICC. Clinical usefulness of hTERC amplification in LBC samples was limited in ICC.

MeSH terms

  • Adult
  • Carcinoma, Squamous Cell / genetics*
  • Case-Control Studies
  • Chromosomes, Human, Pair 3 / chemistry
  • Chromosomes, Human, Pair 3 / genetics
  • Female
  • Gene Amplification*
  • Gene Dosage
  • Humans
  • In Situ Hybridization, Fluorescence
  • RNA
  • RNA, Long Noncoding / genetics*
  • Telomerase / genetics*
  • Uterine Cervical Dysplasia / genetics*
  • Uterine Cervical Neoplasms / genetics*

Substances

  • RNA, Long Noncoding
  • telomerase RNA
  • RNA
  • Telomerase