Retinoic acid is able to induce interferon regulatory factor 1 in squamous carcinoma cells via a STAT-1 independent signalling pathway

Cell Growth Differ. 1999 Apr;10(4):263-70.

Abstract

Interferon regulatory factor 1 (IRF-1) transcription factor binds to DNA sequence elements found in the promoters of type I IFN and IFN-inducible genes. Transient up-regulation of the IRF-1 gene by virus and IFN treatment causes the consequent induction of many IFN-inducible genes involved in cell growth control and apoptosis. We reported recently that IFN-alpha and all-trans retinoic Acid (RA) inhibit the cell proliferation of squamous carcinoma cell line ME-180 by inducing apoptotic cell death. IRF-1 expression correlates with the IFN-alpha-induced apoptosis phenomenon and, surprisingly, with the RA-induced apoptosis phenomenon. To study how these two different ligands cross-talk in the regulation of cellular antitumor responses, the signalling pathways involved in IRF-1 induction were analyzed in RA and/or IFN-alpha-treated ME-180 cells. We provide evidence indicating that RA-induced IRF-1 gene expression is independent of the STAT-1 activation pathway, despite the presence of the IFN-gamma activated sequence element in the gene promoter, but involves nuclear factor-kappaB activation. Thus, here we first describe the activation of nuclear factor-kappaB by both IFN-alpha and RA in the ME-180 cell line. The induced IRF-1 protein is successively able to bind the IFN-stimulated responsive element in the promoter of the target gene 2',5'-oligoadenylate synthetase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Squamous Cell / metabolism*
  • DNA Primers
  • DNA-Binding Proteins / metabolism*
  • DNA-Binding Proteins / physiology*
  • Dactinomycin / pharmacology
  • Electrophoresis, Polyacrylamide Gel
  • Gene Expression Regulation
  • Humans
  • Immunoblotting
  • Interferon Regulatory Factor-1
  • Interferon alpha-2
  • Interferon-alpha / pharmacology
  • NF-kappa B / metabolism
  • Phosphoproteins / metabolism*
  • Protein Synthesis Inhibitors / pharmacology
  • Recombinant Proteins
  • Reverse Transcriptase Polymerase Chain Reaction
  • STAT1 Transcription Factor
  • Signal Transduction*
  • Skin Neoplasms / metabolism*
  • Time Factors
  • Trans-Activators / physiology*
  • Transfection
  • Tretinoin / pharmacology
  • Tretinoin / physiology*
  • Tumor Cells, Cultured

Substances

  • DNA Primers
  • DNA-Binding Proteins
  • IRF1 protein, human
  • Interferon Regulatory Factor-1
  • Interferon alpha-2
  • Interferon-alpha
  • NF-kappa B
  • Phosphoproteins
  • Protein Synthesis Inhibitors
  • Recombinant Proteins
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • Trans-Activators
  • Dactinomycin
  • Tretinoin