Detection of hTERT mRNA in colonic brush specimens as an adjunct to cytopathologic diagnosis of colonic adenocarcinoma

Acta Cytol. 2002 Nov-Dec;46(6):1069-74. doi: 10.1159/000327109.

Abstract

Objective: To investigate the role of reverse transcriptase polymerase chain reaction (RT-PCR) in determining telomerase catalytic subunit (hTERT) mRNA to assist with the diagnosis of colonic adenocarcinoma (CCA) in colonic brush cytology specimens.

Study design: Twenty-seven colonic brushes of CCA were obtained. Initial cytologic diagnoses included CCA, suspicious for CCA (SFC), atypical (ATY) and unsatisfactory. The cytologic specimens were reviewed. A homogeneous RT-PCR assay for hTERT mRNA was performed on 27 colonic brushes of CCA and 24 controls (10 negative brushes, 6 resected CCA and 8 benign colonic mucosa from resected specimens). A RT-PCR assay for beta 2-microglobulin was used as an internal control for mRNA quality.

Results: On review, the initial cytopathologic diagnosis of CCA was confirmed in all 7 cases. In addition, 7 of 19 initially interpreted as SFC and ATY seemed to demonstrate unequivocal cytomorphologic features of malignancy. Telomerase mRNA was more often expressed in CCA than in negative controls in both brush (30%) and resected specimens (57%) (P < .05). Seven cases with hTERT mRNA expression were initially diagnosed as CCA (three), SFC (three) and ATY (one).

Conclusion: CCA may be underdiagnosed in brush cytopathology. The expression of hTERT mRNA may be determined by RT-PCR in brush specimens and may eventually prove to be a useful diagnostic adjunct in the interpretation of inconclusive cases of CCA. Sparse cellularity in brush specimens may result in a relatively low rate of hTERT detection in colonic brushes of CCA; inflammatory changes may contribute to a higher-than-expected rate of hTERT expression in benign colonic epithelium.

MeSH terms

  • Adenocarcinoma / pathology*
  • Biomarkers, Tumor
  • Biopsy
  • Colonic Neoplasms / pathology*
  • DNA-Binding Proteins
  • Gene Expression Regulation, Neoplastic
  • Humans
  • RNA, Messenger / analysis
  • Reverse Transcriptase Polymerase Chain Reaction
  • Telomerase / genetics*
  • beta 2-Microglobulin / genetics

Substances

  • Biomarkers, Tumor
  • DNA-Binding Proteins
  • RNA, Messenger
  • beta 2-Microglobulin
  • Telomerase