Oligodendrocytes Up-regulate the Invasive Activity of Glioblastoma Cells via the Angiopoietin-2 Signaling Pathway

Anticancer Res. 2019 Feb;39(2):577-584. doi: 10.21873/anticanres.13150.

Abstract

Background/aim: Glioblastoma (GBM) is one of the most lethal solid cancers due to its highly invasive nature. The malignant potential of GBM cells might be partially regulated by surrounding normal cells, such as oligodendrocytes or fibroblasts. The aim of this study was to examine the interaction between stromal cells and GBM cells.

Materials and methods: Two GBM cell lines were used. The effect of stromal cells, oligodendrocytes or fibroblasts, on the invasive ability of GBM cells was examined by wound-healing assay and invasion assay.

Results: Oligodendrocytes, in contrast to fibroblasts, significantly increased the migration and invasive ability of GBM cells. Angiopoietin-2 levels were high in the conditioned medium obtained from oligodendrocytes. Angiopoietin-2 significantly increased the motility of GBM, and the motility-stimulating activity of the oligodendrocytes-derived conditioned medium was significantly decreased by anti-angiopoietin-2-neutralizing antibody.

Conclusion: Glioma stromal cells, oligodendrocytes, might up-regulate the invasiveness of GBM cells via angiopoietin-2 signaling.

Keywords: Glioblastoma; angiopoietin-2; fibroblasts; invasion; oligodendrocyte.

MeSH terms

  • Angiopoietin-2 / metabolism*
  • Antibodies, Neutralizing / chemistry
  • Brain Neoplasms / metabolism*
  • Brain Neoplasms / pathology
  • Cell Line, Tumor
  • Cell Movement
  • Cell Proliferation
  • Culture Media, Conditioned
  • Fibroblasts / metabolism
  • Gene Expression Regulation, Neoplastic
  • Glioblastoma / metabolism*
  • Glioblastoma / pathology
  • Glioma / metabolism
  • Humans
  • Neoplasm Invasiveness
  • Oligodendroglia / cytology*
  • Proteome
  • Signal Transduction*
  • Stromal Cells / metabolism
  • Up-Regulation

Substances

  • ANGPT2 protein, human
  • Angiopoietin-2
  • Antibodies, Neutralizing
  • Culture Media, Conditioned
  • Proteome