Characterization of cyclooxygenase in laryngeal papilloma by molecular techniques

Laryngoscope. 1999 Jul;109(7 Pt 1):1137-41. doi: 10.1097/00005537-199907000-00025.

Abstract

Objectives: Demonstrate the induction of cyclooxygenase-2 (COX-2) in laryngeal papilloma Discuss the possible causal role of COX-2 in papilloma formation. Consider the potential for treatment of papilloma using selective COX-2 inhibitors.

Study design: Molecular biological analysis of COX-1 and COX-2 in laryngeal papilloma.

Methods: Tissue samples from five patients with recurrent respiratory papillomatosis (RRP) were analyzed by in situ hybridization, immunohistochemical staining, and reverse transcription polymerase chain reaction (RT-PCR) techniques.

Results: In situ hybridization to COX-2 mRNA showed strong autoradiographic signal surrounding fibrovascular cores. COX-1 autoradiographic signal was low intensity or nondetectable. Normal buccal mucosa biopsies showed low-density or nondetectable autoradiographic signal for both COX-1 and COX-2 mRNAs. In situ hybridization results were corroborated by RT-PCR studies. Levels of COX-2 mRNA were 13-fold more than those in normal mucosa. Immunohistochemical staining for COX-1 and COX-2 showed a similar pattern to that seen with in situ hybridization in both normal and papilloma tissues.

Conclusions: There is an elevation of COX-2 expression in papilloma tissues. This may represent a causal role of COX-2 in the formation and proliferation of laryngeal papilloma. There may also be a role for selective COX-2 inhibition for the treatment of

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Autoradiography
  • Blotting, Southern
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors / therapeutic use
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization
  • Isoenzymes / analysis
  • Laryngeal Neoplasms / drug therapy
  • Laryngeal Neoplasms / enzymology*
  • Membrane Proteins
  • Neoplasm Recurrence, Local / enzymology
  • Papilloma / drug therapy
  • Papilloma / enzymology*
  • Polymerase Chain Reaction
  • Prostaglandin-Endoperoxide Synthases / analysis*
  • RNA-Directed DNA Polymerase

Substances

  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors
  • Isoenzymes
  • Membrane Proteins
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • PTGS1 protein, human
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases
  • RNA-Directed DNA Polymerase