Targeting Glioma Stem Cells: Therapeutic Opportunities and Challenges

Asma Mahdi, Mohamed Aittaleb, Fadel Tissir*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

Abstract

Glioblastoma (GBM), or grade 4 glioma, is the most common and aggressive primary brain tumor in adults with a median survival of 15 months. Increasing evidence suggests that GBM’s aggressiveness, invasiveness, and therapy resistance are driven by glioma stem cells (GSCs), a subpopulation of tumor cells that share molecular and functional characteristics with neural stem cells (NSCs). GSCs are heterogeneous and highly plastic. They evade conventional treatments by shifting their state and entering in quiescence, where they become metabolically inactive and resistant to radiotherapy and chemotherapy. GSCs can exit quiescence and be reactivated to divide into highly proliferative tumor cells which contributes to recurrence. Understanding the molecular mechanisms regulating the biology of GSCs, their plasticity, and the switch between quiescence and mitotic activity is essential to shape new therapeutic strategies. This review examines the latest evidence on GSC biology, their role in glioblastoma progression and recurrence, emerging therapeutic approaches aimed at disrupting their proliferation and survival, and the mechanisms underlying their resistance to therapy.

Original languageEnglish
Article number675
Number of pages28
JournalCells
Volume14
Issue number9
DOIs
Publication statusPublished - 6 May 2025

Keywords

  • Glioma stem cells
  • Plasticity
  • Quiescence
  • Therapeutic targets
  • Therapy resistance

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