UCN-01, a protein kinase C inhibitor, inhibits endothelial cell proliferation and angiogenic hypoxic response

Invasion Metastasis. 1998;18(4):209-18. doi: 10.1159/000024514.

Abstract

Angiogenesis is required for tumor formation and growth; inhibition of angiogenesis is a promising new approach in cancer therapy. UCN-01, a protein kinase C (PKC) inhibitor, induces growth arrest and apoptosis in cancer cells and was recently introduced in a phase I clinical trial. We demonstrate that UCN-01, at concentrations lower than those necessary to inhibit cancer cell growth, inhibit proliferation of human endothelial cells in vitro. Moreover, UCN-01, at concentrations as low as 32 nM, prevent microvessel outgrowth from explant cultures of rat aortic rings. Since hypoxia activates hypoxia-inducible factor (HIF-1)-dependent transcription in cancer cells that, in a paracrine fashion, drive tumor angiogenesis, we investigated the effects of UCN-01 on HIF-1-responsive promoter constructs. We report that, in addition to direct inhibitory effects on endothelial cell growth, UCN-01 abrogates hypoxia-mediated transactivation of HIF-1-responsive promoters in a prostate cancer cell line. We conclude that UCN-01, at clinically relevant concentrations, exerts an anti-neovascularization effect by blocking two important steps in vessel formation: (1) the response of cancer cells to hypoxia, and (2) endothelial cell proliferation.

MeSH terms

  • Alkaloids / pharmacology*
  • Angiogenesis Inhibitors / pharmacology*
  • Animals
  • Aorta, Thoracic / cytology
  • Cell Hypoxia / drug effects*
  • DNA-Binding Proteins / physiology
  • Endothelium, Vascular / drug effects*
  • Endothelium, Vascular / enzymology
  • Endothelium, Vascular / pathology
  • Enzyme Inhibitors / pharmacology*
  • Humans
  • Hypoxia-Inducible Factor 1
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Male
  • Neoplasm Proteins / antagonists & inhibitors*
  • Neovascularization, Pathologic / drug therapy*
  • Nuclear Proteins / physiology
  • Organ Culture Techniques
  • Prostatic Neoplasms / pathology
  • Protein Kinase C / antagonists & inhibitors*
  • Rats
  • Rats, Sprague-Dawley
  • Staurosporine / analogs & derivatives
  • Transcription Factors*
  • Transcription, Genetic / drug effects
  • Tumor Cells, Cultured / drug effects

Substances

  • Alkaloids
  • Angiogenesis Inhibitors
  • DNA-Binding Proteins
  • Enzyme Inhibitors
  • HIF1A protein, human
  • Hif1a protein, rat
  • Hypoxia-Inducible Factor 1
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Neoplasm Proteins
  • Nuclear Proteins
  • Transcription Factors
  • 7-hydroxystaurosporine
  • Protein Kinase C
  • Staurosporine