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Drug Repurposing for Glioblastoma and Current Advances in Drug Delivery-A Comprehensive Review of the Literature
- Source :
- Biomolecules, Biomolecules, Vol 11, Iss 1870, p 1870 (2021)
- Publication Year :
- 2021
-
Abstract
- Glioblastoma (GBM) is the most common primary malignant brain tumor in adults with an extremely poor prognosis. There is a dire need to develop effective therapeutics to overcome the intrinsic and acquired resistance of GBM to current therapies. The process of developing novel anti-neoplastic drugs from bench to bedside can incur significant time and cost implications. Drug repurposing may help overcome that obstacle. A wide range of drugs that are already approved for clinical use for the treatment of other diseases have been found to target GBM-associated signaling pathways and are being repurposed for the treatment of GBM. While many of these drugs are undergoing pre-clinical testing, others are in the clinical trial phase. Since GBM stem cells (GSCs) have been found to be a main source of tumor recurrence after surgery, recent studies have also investigated whether repurposed drugs that target these pathways can be used to counteract tumor recurrence. While several repurposed drugs have shown significant efficacy against GBM cell lines, the blood–brain barrier (BBB) can limit the ability of many of these drugs to reach intratumoral therapeutic concentrations. Localized intracranial delivery may help to achieve therapeutic drug concentration at the site of tumor resection while simultaneously minimizing toxicity and side effects. These strategies can be considered while repurposing drugs for GBM.
- Subjects :
- Clinical Trials as Topic
Brain Neoplasms
Drug Repositioning
repurposed drugs
Antineoplastic Agents
Review
Biochemistry
Microbiology
QR1-502
Gene Expression Regulation, Neoplastic
Drug Delivery Systems
Blood-Brain Barrier
Drug Resistance, Neoplasm
glioma
drug delivery
Neoplastic Stem Cells
Humans
Glioblastoma
Molecular Biology
brain tumor
Signal Transduction
Subjects
Details
- ISSN :
- 2218273X
- Volume :
- 11
- Issue :
- 12
- Database :
- OpenAIRE
- Journal :
- Biomolecules
- Accession number :
- edsair.doi.dedup.....ef0255940ebfa8f3b0337b03e77d29cc