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Molecular Pathways Implicated in Radioresistance of Glioblastoma Multiforme: What Is the Role of Extracellular Vesicles?

Journal

Publisher

MDPI
DOI: 10.3390/ijms24054883

Keywords

glioblastoma multiforme; radioresistance; extracellular vesicles; intercellular communication; stem cells; tumor heterogeneity; tumor microenvironment; hypoxia; metabolic reprogramming; chaperone system; non-coding RNA; DNA repair; theranostics; personalized medicine

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Glioblastoma multiforme (GBM) is an aggressive and treatment-resistant primary brain tumor with high anaplasia and proliferation. Factors contributing to radioresistance include stem cells, tumor heterogeneity, tumor microenvironment, hypoxia, metabolic reprogramming, chaperone system, non-coding RNAs, DNA repair, and extracellular vesicles (EVs). EVs show promise as diagnostic tools and nanodevices for targeted delivery of anticancer agents. Personalized medicine may involve isolating EVs from a GBM patient, modifying them to have anticancer properties, and reinjecting them.
Glioblastoma multiforme (GBM) is a primary brain tumor that is very aggressive, resistant to treatment, and characterized by a high degree of anaplasia and proliferation. Routine treatment includes ablative surgery, chemotherapy, and radiotherapy. However, GMB rapidly relapses and develops radioresistance. Here, we briefly review the mechanisms underpinning radioresistance and discuss research to stop it and install anti-tumor defenses. Factors that participate in radioresistance are varied and include stem cells, tumor heterogeneity, tumor microenvironment, hypoxia, metabolic reprogramming, the chaperone system, non-coding RNAs, DNA repair, and extracellular vesicles (EVs). We direct our attention toward EVs because they are emerging as promising candidates as diagnostic and prognostication tools and as the basis for developing nanodevices for delivering anti-cancer agents directly into the tumor mass. EVs are relatively easy to obtain and manipulate to endow them with the desired anti-cancer properties and to administer them using minimally invasive procedures. Thus, isolating EVs from a GBM patient, supplying them with the necessary anti-cancer agent and the capability of recognizing a specified tissue-cell target, and reinjecting them into the original donor appears, at this time, as a reachable objective of personalized medicine.

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