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Epigenetic regulation of ZBTB18 promotes glioblastoma progression

  • Vita Fedele
  • , Fangping Dai
  • , Anie P. Masilamani
  • , Dieter H. Heiland
  • , Eva Kling
  • , Ana M. Gätjens-Sanchez
  • , Roberto Ferrarese
  • , Leonardo Platania
  • , Doostkam Soroush
  • , Hyunsoo Kim
  • , Sven Nelander
  • , Astrid Weyerbrock
  • , Marco Prinz
  • , Andrea Califano
  • , Antonio Iavarone
  • , Markus Bredel
  • , Maria Carro

Research output: Contribution to journalArticlepeer-review

Abstract

Glioblastoma (GBM) comprises distinct subtypes characterized by their molecular profile. Mesenchymal identity in GBM has been associated with a comparatively unfavorable prognosis, primarily due to inherent resistance of these tumors to current therapies. The identification of molecular determinants of mesenchymal transformation could potentially allow for the discovery of new therapeutic targets. Zinc Finger and BTB Domain Containing 18 (ZBTB18/ZNF238/RP58) is a zinc finger transcriptional repressor with a crucial role in brain development and neuronal differentiation. Here, ZBTB18 is primarily silenced in the mesenchymal subtype of GBM through aberrant promoter methylation. Loss of ZBTB18 contributes to the aggressive phenotype of glioblastoma through regulation of poor prognosis-associated signatures. Restitution of ZBTB18 expression reverses the phenotype and impairs tumor-forming ability. These results indicate that ZBTB18 functions as a tumor suppressor in GBM through the regulation of genes associated with phenotypically aggressive properties.

Original languageEnglish (US)
Pages (from-to)998-1011
Number of pages14
JournalMolecular Cancer Research
Volume15
Issue number8
DOIs
StatePublished - Aug 2017
Externally publishedYes

Bibliographical note

Publisher Copyright:
©2017 AACR.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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