Medulloblastoma cancer stem cells: Molecular signatures and therapeutic targets

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BMJ Publishing Group

Abstract

Medulloblastoma (MB) is the most common malignant primary intracranial neoplasm diagnosed in childhood. Although numerous efforts have been made during the past few years to exploit novel targeted therapies for this aggressive neoplasm, there still exist substantial hitches hindering successful management of MB. Lately, progress in cancer biology has shown evidence that a subpopulation of cells within the tumour, namely cancer stem cells (CSCs), are thought to be responsible for the resistance to most chemotherapeutic agents and radiation therapy, accounting for cancer recurrence. Hence, it is crucial to identify the molecular signatures and genetic aberrations that characterise those CSCs and develop therapies that specifically target them. In this review, we aim to give an overview of the main genetic and molecular cues that depict MB-CSCs and provide a synopsis of the novel therapeutic approaches that specifically target this population of cells to attain enhanced antitumorous effects and therefore overcome resistance to therapy. © Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.

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Brain tumours, Genetics, Molecular oncology, Molecular pathology, Antineoplastic agents, Biomarkers, tumor, Cerebellar neoplasms, Drug resistance, neoplasm, Gene expression regulation, neoplastic, Humans, Medulloblastoma, Neoplastic stem cells, Antineoplastic agent, Cd133 antigen, Myc protein, Phosphatidylinositol 3 kinase, Polycomb group protein, Sonic hedgehog protein, Urokinase receptor, Tumor marker, Antineoplastic activity, Cancer chemotherapy, Cancer classification, Cancer radiotherapy, Cancer recurrence, Cancer stem cell, Hedgehog signaling, Human, Nonhuman, Priority journal, Recurrent disease, Review, Cerebellum tumor, Drug effect, Drug resistance, Gene expression regulation, Metabolism, Physiology

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