T-oligo treatment decreases constitutive and UVB-induced COX-2 levels through p53- and NFkappaB-dependent repression of the COX-2 promoter

J Biol Chem. 2005 Sep 16;280(37):32379-88. doi: 10.1074/jbc.M503245200. Epub 2005 Jul 26.

Abstract

Chronically irradiated murine skin and UV light-induced squamous cell carcinomas overexpress the inducible isoform of cyclooxygenase (COX-2), and COX-2 inhibition reduces photocarcinogenesis in mice. We have reported previously that DNA oligonucleotides substantially homologous to the telomere 3'-overhang (T-oligos) induce DNA repair capacity and multiple other cancer prevention responses, in part through up-regulation and activation of p53. To determine whether T-oligos affect COX-2 expression, human newborn keratinocytes and fibroblasts were pretreated with T-oligos or diluent alone for 24 h, UV-irradiated, and processed for Western blotting. In both cell types, T-oligos transcriptionally down-regulated base-line and UV light-induced COX-2 expression, coincident with p53 activation. In fibroblasts with wild type versus dominant negative p53 (p53(WT) versus p53(DN)), T-oligos decreased constitutive expression of a COX-2 reporter plasmid by >50%. We then examined NFkappaB, a known positive regulator of COX-2 transcription. In p53(WT) but not in p53(DN) fibroblasts and in human keratinocytes, T-oligos decreased readout of an NFkappaB promoter-driven reporter plasmid and decreased NFkappaB binding to DNA. After T-oligo treatment and subsequent UV irradiation, binding of the transcriptional co-activator protein p300 to NFkappaB was decreased, whereas binding of p300 to p53 was increased. Human skin explants provided with T-oligos had markedly decreased COX-2 immunostaining both at base-line and post-UV light, coincident with increased p53 immunostaining. We conclude that T-oligos transcriptionally down-regulate COX-2 expression in human skin via activation and up-regulation of p53, at least in part by inhibiting NFkappaB transcriptional activation. Decreased COX-2 expression may contribute to the observed ability of T-oligos to reduce photocarcinogenesis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acetyltransferases / metabolism
  • Adult
  • Aged
  • Blotting, Western
  • Cell Cycle Proteins / metabolism
  • Cells, Cultured
  • Cyclooxygenase 2
  • DNA / chemistry
  • DNA Repair
  • Down-Regulation
  • Fibroblasts / metabolism
  • Gene Expression Regulation, Enzymologic*
  • Histone Acetyltransferases
  • Humans
  • Immunoblotting
  • Immunohistochemistry
  • Keratinocytes / metabolism
  • Light
  • Membrane Proteins
  • Microscopy, Fluorescence
  • Middle Aged
  • NF-kappa B / metabolism*
  • Oligonucleotides / chemistry
  • Promoter Regions, Genetic*
  • Prostaglandin-Endoperoxide Synthases / biosynthesis*
  • Prostaglandin-Endoperoxide Synthases / genetics*
  • Protein Isoforms
  • Skin / metabolism
  • Transcription Factors / metabolism
  • Transcriptional Activation
  • Transfection
  • Tumor Suppressor Protein p53 / metabolism*
  • Ultraviolet Rays*
  • Up-Regulation
  • p300-CBP Transcription Factors

Substances

  • Cell Cycle Proteins
  • Membrane Proteins
  • NF-kappa B
  • Oligonucleotides
  • Protein Isoforms
  • Transcription Factors
  • Tumor Suppressor Protein p53
  • DNA
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases
  • Acetyltransferases
  • Histone Acetyltransferases
  • p300-CBP Transcription Factors
  • p300-CBP-associated factor