Cancer stem cells in neuroblastoma: Expanding the therapeutic frontier
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Frontiers Media S.A.
Abstract
Neuroblastoma (NB) is the most common extracranial solid tumor often diagnosed in childhood. Despite intense efforts to develop a successful treatment, current available therapies are still challenged by high rates of resistance, recurrence and progression, most notably in advanced cases and highly malignant tumors. Emerging evidence proposes that this might be due to a subpopulation of cancer stem cells (CSCs) or tumor-initiating cells (TICs) found in the bulk of the tumor. Therefore, the development of more targeted therapy is highly dependent on the identification of the molecular signatures and genetic aberrations characteristic to this subpopulation of cells. This review aims at providing an overview of the key molecular players involved in NB CSCs and focuses on the experimental evidence from NB cell lines, patient-derived xenografts and primary tumors. It also provides some novel approaches of targeting multiple drivers governing the stemness of CSCs to achieve better anti-tumor effects than the currently used therapeutic agents. © 2019 Bahmad, Chamaa, Assi, Chalhoub, Abou-Antoun and Abou-Kheir.
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Keywords
Cancer stem cells, Genetic aberrations, Molecular signatures, Neuroblastoma, Therapeutic targets, Abc transporter subfamily g, Aldehyde dehydrogenase isoenzyme 1, Bmi1 protein, Breast cancer resistance protein, Cd133 antigen, Cd24 antigen, Cisplatin, Clomipramine, Colony stimulating factor receptor, Frizzled protein, Hermes antigen, Hypoxia inducible factor 1alpha, Hypoxia inducible factor 2alpha, Lamin a, Lamin c, Leucine rich repeat kinase 2, Lithium chloride, Matrix metalloproteinase, Nestin, Nuclear receptor nr4a3, Polo like kinase 1, Probenecid, Rapamycin, Retinoblastoma binding protein 1, Retinoic acid, Stat3 protein, Stem cell factor receptor, Temozolomide, Transient receptor potential channel 7, Unindexed drug, Akt signaling, Antineoplastic activity, Apoptosis, Breast cancer, Cancer recurrence, Cancer resistance, Cancer stem cell, Carcinogenesis, Cell proliferation, Chromosome aberration, Clonogenesis, Dlk1 gene, Down regulation, Epigenetics, Gene, Gene expression, Gene knockdown, Gene overexpression, Glioma, Hif gene, Histology, Human, Hypoxia, Lung cancer, Lymphocyte subpopulation, Microarray analysis, Molecularly targeted therapy, Protein expression, Review, Rhabdomyosarcoma, Stomach cancer, Thyroid cancer, Wnt signaling, Xenograft