Polycomb-mediated repression of EphrinA5 promotes growth and invasion of glioblastoma

Oncogene. 2020 Mar;39(12):2523-2538. doi: 10.1038/s41388-020-1161-3. Epub 2020 Jan 27.

Abstract

Glioblastoma (GBM) is the most common and most aggressive intrinsic brain tumour in adults. Integrated transcriptomic and epigenomic analyses of glioblastoma initiating cells (GIC) in a mouse model uncovered a novel epigenetic regulation of EfnA5. In this model, Bmi1 enhances H3K27me3 at the EfnA5 locus and reinforces repression of selected target genes in a cellular context-dependent fashion. EfnA5 mediates Bmi1-dependent proliferation and invasion in vitro and tumour formation in an allograft model. Importantly, we show that this novel Polycomb feed-forward loop is also active in human GIC and we provide pre-clinical evidence of druggability of the EFNA5 signalling pathway in GBM xenografts overexpressing Bmi1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antihypertensive Agents / pharmacology
  • Cell Proliferation
  • Doxazosin / pharmacology
  • Drug Delivery Systems
  • Ephrin-A5 / antagonists & inhibitors
  • Ephrin-A5 / metabolism*
  • Epigenesis, Genetic
  • Gene Expression Regulation, Neoplastic
  • Glioblastoma / metabolism*
  • Glioblastoma / pathology
  • Histones / metabolism
  • Humans
  • Lysine / metabolism
  • Mice
  • Mice, Transgenic
  • Neoplasm Invasiveness
  • Neural Stem Cells / metabolism
  • Neurogenesis
  • Polycomb Repressive Complex 1 / genetics
  • Polycomb Repressive Complex 1 / metabolism*
  • Tumor Cells, Cultured

Substances

  • Antihypertensive Agents
  • BMI1 protein, human
  • Ephrin-A5
  • Histones
  • Polycomb Repressive Complex 1
  • Lysine
  • Doxazosin