p190RhoGAP can act to inhibit PDGF-induced gliomas in mice: a putative tumor suppressor encoded on human chromosome 19q13.3

Genes Dev. 2003 Feb 15;17(4):476-87. doi: 10.1101/gad.1040003.

Abstract

p190RhoGAP and Rho are key regulators of oligodendrocyte differentiation. The gene encoding p190RhoGAP is located at 19q13.3 of the human chromosome, a locus that is deleted in 50%-80% of oligodendrogliomas. Here we provide evidence that p190RhoGAP may suppress gliomagenesis by inducing a differentiated glial phenotype. Using a cell culture model of autocrine loop PDGF stimulation, we show that reduced Rho activity via p190RhoGAP overexpression or Rho kinase inhibition induced cellular process extension, a block in proliferation, and reduced expression of the neural precursor marker nestin. In vivo infection of mice with retrovirus expressing PDGF and the p190 GAP domain caused a decreased incidence of oligodendrogliomas compared with that observed with PDGF alone. Independent experiments revealed that the retroviral vector insertion site in 3 of 50 PDGF-induced gliomas was within the p190RhoGAP gene. This evidence strongly suggests that p190 regulates critical components of PDGF oncogenesis and can act as a tumor suppressor in PDGF-induced gliomas by down-regulating Rho activity.

Publication types

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

MeSH terms

  • Animals
  • Brain Neoplasms / genetics
  • Brain Neoplasms / pathology*
  • Cell Differentiation / drug effects
  • Cell Differentiation / genetics
  • Cells, Cultured
  • Chromosomes, Human, Pair 19
  • DNA-Binding Proteins
  • Down-Regulation
  • GTPase-Activating Proteins
  • Genes, Tumor Suppressor
  • Glioma / genetics
  • Glioma / metabolism
  • Glioma / pathology*
  • Guanine Nucleotide Exchange Factors / genetics
  • Guanine Nucleotide Exchange Factors / metabolism*
  • Humans
  • Intermediate Filament Proteins / metabolism
  • Mice
  • Mice, Inbred Strains
  • Nerve Tissue Proteins*
  • Nestin
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • Oligodendroglioma / genetics
  • Oligodendroglioma / pathology
  • Phthalazines / pharmacology
  • Platelet-Derived Growth Factor / drug effects
  • Platelet-Derived Growth Factor / genetics
  • Platelet-Derived Growth Factor / metabolism*
  • Pyridines*
  • Repressor Proteins
  • Retroviridae / genetics

Substances

  • ARHGAP35 protein, human
  • ARHGAP5 protein, human
  • Arhgap35 protein, mouse
  • Arhgap5 protein, mouse
  • DNA-Binding Proteins
  • GTPase-Activating Proteins
  • Guanine Nucleotide Exchange Factors
  • Intermediate Filament Proteins
  • NES protein, human
  • Nerve Tissue Proteins
  • Nes protein, mouse
  • Nestin
  • Nuclear Proteins
  • Phthalazines
  • Platelet-Derived Growth Factor
  • Pyridines
  • Repressor Proteins
  • vatalanib