TY - JOUR
T1 - The Complexity of Malignant Glioma Treatment
AU - Kampers, Linde F.C.
AU - Metselaar, Dennis S.
AU - Vinci, Maria
AU - Scirocchi, Fabio
AU - Veldhuijzen van Zanten, Sophie
AU - Eyrich, Matthias
AU - Biassoni, Veronica
AU - Hulleman, Esther
AU - Karremann, Michael
AU - Stücker, Wilfried
AU - Van Gool, Stefaan W.
N1 - Publisher Copyright:
© 2025 by the authors.
PY - 2025/3/4
Y1 - 2025/3/4
N2 - 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.
AB - 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.
KW - immunotherapy
KW - malignant glioma
KW - tumor microenvironment
UR - https://www.scopus.com/pages/publications/86000801729
UR - https://www.mendeley.com/catalogue/03f2715b-29e9-368d-9fd8-86f11830fb6f/
U2 - 10.3390/cancers17050879
DO - 10.3390/cancers17050879
M3 - Review article
C2 - 40075726
AN - SCOPUS:86000801729
SN - 2072-6694
VL - 17
JO - Cancers
JF - Cancers
IS - 5
M1 - 879
ER -