Cancer stem cells in neuroblastoma: Expanding the therapeutic frontier

dc.contributor.authorBahmad, Hisham F.
dc.contributor.authorChamaa, Farah
dc.contributor.authorAssi, Sahar
dc.contributor.authorChalhoub, Reda M.
dc.contributor.authorAbou-Antoun, Tamara J.
dc.contributor.authorAbou-Kheir, Wassim G.
dc.contributor.departmentAnatomy, Cell Biology, and Physiological Sciences
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:36:46Z
dc.date.available2025-01-24T11:36:46Z
dc.date.issued2019
dc.description.abstractNeuroblastoma (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.
dc.identifier.doihttps://doi.org/10.3389/fnmol.2019.00131
dc.identifier.eid2-s2.0-85069532083
dc.identifier.urihttp://hdl.handle.net/10938/28713
dc.language.isoen
dc.publisherFrontiers Media S.A.
dc.relation.ispartofFrontiers in Molecular Neuroscience
dc.sourceScopus
dc.subjectCancer stem cells
dc.subjectGenetic aberrations
dc.subjectMolecular signatures
dc.subjectNeuroblastoma
dc.subjectTherapeutic targets
dc.subjectAbc transporter subfamily g
dc.subjectAldehyde dehydrogenase isoenzyme 1
dc.subjectBmi1 protein
dc.subjectBreast cancer resistance protein
dc.subjectCd133 antigen
dc.subjectCd24 antigen
dc.subjectCisplatin
dc.subjectClomipramine
dc.subjectColony stimulating factor receptor
dc.subjectFrizzled protein
dc.subjectHermes antigen
dc.subjectHypoxia inducible factor 1alpha
dc.subjectHypoxia inducible factor 2alpha
dc.subjectLamin a
dc.subjectLamin c
dc.subjectLeucine rich repeat kinase 2
dc.subjectLithium chloride
dc.subjectMatrix metalloproteinase
dc.subjectNestin
dc.subjectNuclear receptor nr4a3
dc.subjectPolo like kinase 1
dc.subjectProbenecid
dc.subjectRapamycin
dc.subjectRetinoblastoma binding protein 1
dc.subjectRetinoic acid
dc.subjectStat3 protein
dc.subjectStem cell factor receptor
dc.subjectTemozolomide
dc.subjectTransient receptor potential channel 7
dc.subjectUnindexed drug
dc.subjectAkt signaling
dc.subjectAntineoplastic activity
dc.subjectApoptosis
dc.subjectBreast cancer
dc.subjectCancer recurrence
dc.subjectCancer resistance
dc.subjectCancer stem cell
dc.subjectCarcinogenesis
dc.subjectCell proliferation
dc.subjectChromosome aberration
dc.subjectClonogenesis
dc.subjectDlk1 gene
dc.subjectDown regulation
dc.subjectEpigenetics
dc.subjectGene
dc.subjectGene expression
dc.subjectGene knockdown
dc.subjectGene overexpression
dc.subjectGlioma
dc.subjectHif gene
dc.subjectHistology
dc.subjectHuman
dc.subjectHypoxia
dc.subjectLung cancer
dc.subjectLymphocyte subpopulation
dc.subjectMicroarray analysis
dc.subjectMolecularly targeted therapy
dc.subjectProtein expression
dc.subjectReview
dc.subjectRhabdomyosarcoma
dc.subjectStomach cancer
dc.subjectThyroid cancer
dc.subjectWnt signaling
dc.subjectXenograft
dc.titleCancer stem cells in neuroblastoma: Expanding the therapeutic frontier
dc.typeReview

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