Activation of Sp1-mediated vascular permeability factor/vascular endothelial growth factor transcription requires specific interaction with protein kinase C zeta

J Biol Chem. 1998 Oct 9;273(41):26277-80. doi: 10.1074/jbc.273.41.26277.

Abstract

The transcription factor Sp1 is ubiquitously expressed and plays a significant role in the constitutive and induced expression of a variety of mammalian genes and may even contribute to tumorigenesis. Here, we describe a novel pathway whereby Sp1 promotes the transcription of vascular permeability factor/vascular endothelial growth factor (VPF/VEGF), a potent angiogenic factor, by interacting directly and specifically with protein kinase C zeta (PKC zeta) isoform in renal cell carcinoma. PKC zeta binds and phosphorylates the zinc finger region of Sp1. Moreover, in the presence of the wild type von Hippel-Lindau gene product, the interaction of Sp1 with PKC zeta is inhibited, and in this manner steady state levels of Sp1 phosphorylation are decreased significantly. Co-transfection of renal cell carcinoma cells and human fibrosarcoma cells with a plasmid overexpressing PKC zeta and VPF/VEGF promoter luciferase constructs results in activation of Sp1-mediated transcription, whereas expression of a dominant-negative mutant of PKC zeta repressed this activation. Taken together, our results suggest a new pathway of cell signaling through PKC zeta and provide an insight into PKC zeta and Sp1-dependent transcriptional regulation of VPF/VEGF expression and thus tumor angiogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Renal Cell / enzymology
  • Carcinoma, Renal Cell / metabolism
  • Carcinoma, Renal Cell / pathology
  • Endothelial Growth Factors / genetics*
  • Fibrosarcoma / enzymology
  • Fibrosarcoma / metabolism
  • Fibrosarcoma / pathology
  • Humans
  • Kidney Neoplasms / enzymology
  • Kidney Neoplasms / metabolism
  • Kidney Neoplasms / pathology
  • Ligases*
  • Lymphokines / genetics*
  • Phosphorylation
  • Promoter Regions, Genetic
  • Protein Binding
  • Protein Kinase C / metabolism*
  • Proteins / metabolism
  • Recombinant Fusion Proteins / metabolism
  • Sp1 Transcription Factor / metabolism*
  • Transcription, Genetic*
  • Tumor Cells, Cultured
  • Tumor Suppressor Proteins*
  • Ubiquitin-Protein Ligases*
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors
  • Von Hippel-Lindau Tumor Suppressor Protein

Substances

  • Endothelial Growth Factors
  • Lymphokines
  • Proteins
  • Recombinant Fusion Proteins
  • Sp1 Transcription Factor
  • Tumor Suppressor Proteins
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors
  • Ubiquitin-Protein Ligases
  • Von Hippel-Lindau Tumor Suppressor Protein
  • protein kinase C zeta
  • Protein Kinase C
  • Ligases
  • VHL protein, human