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Recent advances in glioblastoma multiforme therapy: A focus on autophagy regulation
Mehdi Sanati1, Maryam Moradi Binabaj2, Seyed Sajad Ahmadi3
1Department of Pharmacology and Toxicology, Faculty of Pharmacy, Birjand University of Medical Sciences, Birjand, Iran; Experimental and Animal Study Center, Birjand University of Medical Sciences, Birjand, Iran.
Abstract:
Despite conventional treatment options including chemoradiation, patients with the most aggressive primary brain tumor, glioblastoma multiforme (GBM), experience an average survival time of less than 15 months. Regarding the malignant nature of GBM, extensive research and discovery of novel treatments are urgently required to improve the patients' prognosis. Autophagy, a crucial physiological pathway for the degradation and recycling of cell components, is one of the exciting targets of GBM studies. Interventions aimed at autophagy activation or inhibition have been explored as potential GBM therapeutics. This review, which delves into therapeutic techniques to block or activate autophagy in preclinical and clinical research, aims to expand our understanding of available therapies battling GBM.
Insights
Glioblastoma multiforme (GBM) is an aggressive brain cancer with poor survival rates. Targeting autophagy, a cellular recycling process, offers promising new therapeutic strategies for GBM treatment.
Area of Science:
- Oncology
- Cell Biology
- Neuro-oncology
Background:
- Glioblastoma multiforme (GBM) is an aggressive primary brain tumor with a median survival of under 15 months despite conventional treatments like chemoradiation.
- Novel therapeutic strategies are urgently needed to improve patient prognosis for GBM.
- Autophagy, a fundamental cellular process for degrading and recycling cellular components, is increasingly recognized as a potential therapeutic target in GBM.
Purpose of the Study:
- To review current therapeutic strategies targeting autophagy in glioblastoma multiforme (GBM).
- To explore the potential of modulating autophagy (activation or inhibition) as a treatment for GBM.
- To consolidate preclinical and clinical findings on autophagy-modulating therapies for GBM.
Main Methods:
- Systematic review of preclinical and clinical research studies.
- Analysis of therapeutic interventions focused on modulating autophagy in GBM models and patients.
- Synthesis of data on the efficacy and mechanisms of autophagy-targeting agents.
Main Results:
- Autophagy modulation (both activation and inhibition) has shown potential in preclinical GBM models.
- Specific agents targeting autophagy pathways are under investigation in clinical trials for GBM.
- Understanding the dual role of autophagy in GBM is crucial for developing effective therapies.
Conclusions:
- Targeting autophagy represents a promising avenue for novel glioblastoma multiforme (GBM) therapeutics.
- Further research is needed to optimize autophagy-modulating strategies for clinical application in GBM.
- Modulating autophagy holds potential to improve survival outcomes for GBM patients.
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