Increased invasive phenotype of CSF-1R expression in glioma cells via the ERK1/2 signaling pathway

Cancer Gene Ther. 2019 May;26(5-6):136-144. doi: 10.1038/s41417-018-0053-y. Epub 2018 Oct 26.

Abstract

Glioma is a common malignant tumor of the central nervous system (CNS) that has no effective treatment. In this study, we report that colony-stimulating factor-1 receptor (CSF-1R) is a key mediator of malignant features in glioma via modulation of the activity of extracellular signal-regulated kinase 1/2 (ERK1/2) signaling. In general, CSF-1R upregulation in glioma is associated with poor histologic grade and sursvival. Enforced expression of CSF-1R is sufficient to enhance cell growth, migration, invasion, and epithelial-mesenchymal transition, while CSF-1R silencing suppresses the above-described malignant phenotypes. Mechanistic investigations show that CSF-1R promotes activation of the ERK1/2 signaling pathway. Inhibition of the ERK1/2 pathway by SCH772984 reduces CSF-1R-induced migration, invasion, and lung metastasis of glioma cells, thus establishing a role of the ERK1/2 signaling pathway in mediating the CSF-1R effect. In summary, our results suggest that CSF-1R overexpression in gliomas contributes to the malignant behaviors of cancer cells.

MeSH terms

  • Animals
  • Brain Neoplasms / genetics
  • Brain Neoplasms / metabolism*
  • Brain Neoplasms / pathology
  • Cell Line, Tumor
  • Cell Movement / physiology
  • Cell Proliferation / physiology
  • Disease Models, Animal
  • G1 Phase Cell Cycle Checkpoints
  • Glioma / genetics
  • Glioma / metabolism*
  • Glioma / pathology
  • Heterografts
  • Humans
  • MAP Kinase Signaling System*
  • Mice
  • Mice, Nude
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3 / metabolism
  • Phenotype
  • Receptor, Macrophage Colony-Stimulating Factor / biosynthesis*
  • Receptor, Macrophage Colony-Stimulating Factor / genetics
  • S Phase
  • Transfection
  • Up-Regulation

Substances

  • Receptor, Macrophage Colony-Stimulating Factor
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3