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The Complexity of Malignant Glioma Treatment

  • Linde F.C. Kampers
  • , Dennis S. Metselaar
  • , Maria Vinci
  • , Fabio Scirocchi
  • , Sophie Veldhuijzen van Zanten
  • , Matthias Eyrich
  • , Veronica Biassoni
  • , Esther Hulleman
  • , Michael Karremann
  • , Wilfried Stücker
  • , Stefaan W. Van Gool

Onderzoeksoutput: Bijdrage aan tijdschriftArtikel recenserenpeer review

8 Citaten (Scopus)

Samenvatting

Malignant glioma is a highly aggressive, therapeutically non-responsive, and deadly disease with a unique tumor microenvironment (TME). Of the 14 currently recognized and described cancer hallmarks, five are especially implicated in malignant glioma and targetable with repurposed drugs: cancer stem-like cells, in general, and glioma stem-like cells in particular (GSCs), vascularization and hypoxia, metabolic reprogramming, tumor-promoting inflammation and sustained proliferative signaling. Each hallmark drives malignant glioma development, both individually and through interactions with other hallmarks, in which the TME plays a critical role. To combat the aggressive malignant glioma spatio-temporal heterogeneity driven by TME interactions, and to overcome its therapeutic challenges, a combined treatment strategy including anticancer therapies, repurposed drugs and multimodal immunotherapy should be the aim for future treatment approaches.

Originele taal-2Engels
Artikelnummer879
TijdschriftCancers
Volume17
Nummer van het tijdschrift5
DOI's
StatusGepubliceerd - 4 mrt 2025

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