Tumoroid Model Reveals Synergistic Impairment of Metabolism by Iron Chelators and Temozolomide in Chemo-Resistant Patient-derived Glioblastoma Cells

Adv Sci (Weinh). 2025 May;12(20):e2412505. doi: 10.1002/advs.202412505. Epub 2025 Apr 26.

Abstract

Chemoresistance poses a significant clinical challenge in managing glioblastoma (GBM), limiting the long-term success of traditional treatments. Here, a 3D tumoroid model is used to investigate the metabolic sensitivity of temozolomide (TMZ)-resistant GBM cells to iron chelation by deferoxamine (DFO) and deferiprone (DFP). This work shows that TMZ-resistant GBM cells acquire stem-like characteristics, higher intracellular iron levels, higher expression of aconitase, and elevated reliance on oxidative phosphorylation and proteins associated with iron metabolism. Using a microphysiological model of GBM-on-a-chip consisting of extracellular matrix (ECM)-incorporated tumoroids, this work demonstrates that the combination of iron chelators with TMZ induces a synergistic effect on an in vitro tumoroid model of newly diagnosed and recurrent chemo-resistant patient-derived GBM and reduced their size and invasion. Investigating downstream metabolic variations reveal reduced intracellular iron, increased reactive oxygen species (ROS), upregulated hypoxia-inducible factor-1α, reduced viability, increased autophagy, upregulated ribonucleotide reductase (RRM2), arrested proliferation, and induced cell death in normoxic TMZ-resistant cells. Hypoxic cells, while showing similar results, display reduced responses to iron deficiency, less blebbing, and an induced autophagic flux, suggesting an adaptive mechanism associated with hypoxia. These findings show that co-treatment with iron chelators and TMZ induces a synergistic effect, making this combination a promising GBM therapy.

Keywords: chemoresistance; glioblastoma; iron metabolism; metabolic sensitivity; tumoroid model.

MeSH terms

  • Brain Neoplasms* / drug therapy
  • Brain Neoplasms* / metabolism
  • Cell Line, Tumor
  • Deferiprone / pharmacology
  • Deferoxamine / pharmacology
  • Drug Resistance, Neoplasm* / drug effects
  • Drug Synergism
  • Glioblastoma* / drug therapy
  • Glioblastoma* / metabolism
  • Glioblastoma* / pathology
  • Humans
  • Iron / metabolism
  • Iron Chelating Agents* / pharmacology
  • Reactive Oxygen Species / metabolism
  • Temozolomide* / pharmacology

Substances

  • Temozolomide
  • Iron Chelating Agents
  • Reactive Oxygen Species
  • Deferoxamine
  • Deferiprone
  • Iron