Skip to main navigation Skip to search Skip to main content

DNA methylation–based deconvolution study of glioblastoma heterogeneity and identification of cell compositions associated with patient survival

  • Aviel Iluz
  • , Nir Lavi
  • , Hanna Charbit
  • , Mijal Gutreiman
  • , Masha Idelson
  • , Debora Steiner
  • , Etti Ben-Shushan
  • , Aviad Zick
  • , Amir Eden
  • , Anat Mordechai
  • , Moscovici Samuel
  • , Yakov Fellig
  • , Alexander Lossos
  • , Joshua Moss
  • , Benjamin E. Reubinoff
  • , Iris Lavon*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Background Isocitrate dehydrogenase (IDH)-wildtype glioblastoma (GBM) is an aggressive, heterogeneous brain tumor with limited treatment options. This study employs DNA methylation-based deconvolution of GBM to define its cellular composition and its association with patient outcomes. Methods We generated oligodendroglial precursor cells at various developmental stages from enriched human neural progenitor cultures and used their DNA methylation signatures, along with published signatures of brain tumor cell types and the tumor microenvironment, to deconvolve 263 adult GBMs (Heidelberg cohort). An independent cohort of 199 GBMs from The Cancer Genome Atlas (TCGA) and GEO, all treated with standard-of-care therapy, was similarly deconvolved. Kaplan-Meier survival analysis was used to assess the prognostic value of the neoplastic components. Results GBM deconvolution uncovered distinct cellular compositions that differed between the neoplastic and non-neoplastic component. The neoplastic fractions averaged 70% of the tumor bulk and were predominantly composed of oligodendrocyte-like (43%) cell populations, in addition to oligodendrocyte precursor-like (27%), astrocyte-like (19%), and mesenchymal stem cell-like (11%) populations. The non-neoplastic fractions were enriched for macrophages, vascular cells, and immune cell populations. A higher oligodendrocyte-like signature was linked to poorer survival (median survival 14.3 vs. 15.3 months; P = .017), while a higher astrocyte-like signature correlated with improved survival (15.3 vs. 13.4 months; P = .044). Further, a higher astrocyte-to-oligodendrocyte ratio was associated with significantly longer survival (15.8 vs. 11.9 months; P < .00011). Conclusions The methylation-based deconvolution data and analyses provided insight into GBM heterogeneity and highlighted the prognostic potential of the astrocyte-to-oligodendrocyte ratio and its application in personalized treatment strategies.

Original languageEnglish
JournalNeuro-Oncology Advances
Volume8
Issue number1
DOIs
StatePublished - 1 Jan 2026

Bibliographical note

Publisher Copyright:
© The Author(s) 2026. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology.

Keywords

  • central nervous system tumor
  • deconvolution
  • methylation signature
  • tumor heterogeneity
  • ­glioblastoma

Fingerprint

Dive into the research topics of 'DNA methylation–based deconvolution study of glioblastoma heterogeneity and identification of cell compositions associated with patient survival'. Together they form a unique fingerprint.

Cite this