The Hippo-TAZ axis mediates vascular endothelial growth factor C in glioblastoma-derived exosomes to promote angiogenesis

Cancer Lett. 2021 Aug 10:513:1-13. doi: 10.1016/j.canlet.2021.05.002. Epub 2021 May 16.

Abstract

Glioblastoma (GBM) is one of the most highly vascularized human cancers. The role of exosomes in cancer angiogenesis has attracted recent interest. However, proangiogenic biomolecules transported by exosomes to facilitate angiogenesis in GBM have not yet been identified. Here, we found a specific 120-kDa isoform of vascular endothelial growth factor (VEGF) in GBM-derived exosomes and confirmed it as VEGF-C. By binding to VEGF receptor 2 (VEGFR2), VEGF-C from GBM-derived exosomes showed a strong stimulatory effect on tafazzin (TAZ) expression in endothelial cells by inhibiting the Hippo signaling pathway, which eventually stimulates endothelial cell viability, migration, and tubulation. In human glioma samples, the expression of VEGF-C in tumor cells positively correlated with TAZ expression in endothelial cells. We further demonstrated that an inhibitor of exosomal release had a cooperative inhibitory effect with bevacizumab on GBM xenograft subcutaneous tumor growth and angiogenesis. Taken together, our findings revealed a novel VEGF-C isoform in GBM-derived exosomes with a role in angiogenesis and highlighted the importance of recognizing its unique signaling pathway when considering drug treatment strategies for GBM.

Keywords: Angiogenesis; Bevacizumab; Exosome; GBM; VEGF-C.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Animals
  • Brain Neoplasms / blood supply*
  • Brain Neoplasms / metabolism
  • Cell Line, Tumor
  • Exosomes / metabolism*
  • Female
  • Glioblastoma / blood supply*
  • Glioblastoma / metabolism
  • Heterografts
  • Hippo Signaling Pathway
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Neovascularization, Pathologic / metabolism
  • Neovascularization, Pathologic / pathology
  • Protein Serine-Threonine Kinases / metabolism*
  • Signal Transduction
  • Transcriptional Coactivator with PDZ-Binding Motif Proteins
  • Vascular Endothelial Growth Factor C / metabolism*

Substances

  • Intracellular Signaling Peptides and Proteins
  • Transcriptional Coactivator with PDZ-Binding Motif Proteins
  • VEGFC protein, human
  • Vascular Endothelial Growth Factor C
  • WWTR1 protein, human
  • Protein Serine-Threonine Kinases