Repurposing of Anticancer Stem Cell Drugs in Brain Tumors
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SAGE Publications Ltd
Abstract
Brain tumors in adults may be infrequent when compared with other cancer etiologies, but they remain one of the deadliest with bleak survival rates. Current treatment modalities encompass surgical resection, chemotherapy, and radiotherapy. However, increasing resistance rates are being witnessed, and this has been attributed, in part, to cancer stem cells (CSCs). CSCs are a subpopulation of cancer cells that reside within the tumor bulk and have the capacity for self-renewal and can differentiate and proliferate into multiple cell lineages. Studying those CSCs enables an increasing understanding of carcinogenesis, and targeting CSCs may overcome existing treatment resistance. One approach to weaponize new drugs is to target these CSCs through drug repurposing which entails using drugs, which are Food and Drug Administration–approved and safe for one defined disease, for a new indication. This approach serves to save both time and money that would otherwise be spent in designing a totally new therapy. In this review, we will illustrate drug repurposing strategies that have been used in brain tumors and then further elaborate on how these approaches, specifically those that target the resident CSCs, can help take the field of drug repurposing to a new level. © The Author(s) 2021.
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Angiogenesis, Brain tumors, Cancer stem cells, Drug repurposing, Glioblastoma, Meningioma, Stemness, Tumor heterogeneity, Tumor immune infiltrate, Tumor microenvironment, Anthelmintics, Antineoplastic agents, Biomarkers, tumor, Brain neoplasms, Cell differentiation, Cell proliferation, Drug approval, Drug repositioning, Humans, Hypoglycemic agents, Molecular targeted therapy, Neoplastic stem cells, United states, United states food and drug administration, Aldehyde dehydrogenase, Anthelmintic agent, Anticonvulsive agent, Antidepressant agent, Antidiabetic agent, Antihypertensive agent, Antilipemic agent, Antineoplastic agent, Cell surface marker, Glycogen synthase kinase 3 inhibitor, Glycogen synthase kinase 3beta, Neuroleptic agent, Nonsteroid antiinflammatory agent, Transcription factor, Tumor marker, Adult, Asymmetric cell division, Brain tumor, Cancer chemotherapy, Cancer stem cell, Cell lineage, Cell subpopulation, Childhood cancer, Drug cost, Drug efficacy, Drug safety, Enzyme activity, Human, Human cell, Investment, Nonhuman, Population research, Repeat procedure, Review, Stem cell self-renewal, Time, Tumor gene, Cytology, Drug effect, Food and drug administration, Molecularly targeted therapy, Procedures