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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorAlmazan Moga, Ana
dc.contributor.authorZarzosa Martinez, Patricia
dc.contributor.authorVidal Marin, Isaac
dc.contributor.authorMolist Muñoz, Carla
dc.contributor.authorGiralt Buch, Irina
dc.contributor.authorSoriano Fernández, Aroa
dc.contributor.authorSegura Ginard, Miguel
dc.contributor.authorSánchez de Toledo Codina, Josep
dc.contributor.authorRoma Castanyer, Josep
dc.contributor.authorGallego Melcón, Soledad
dc.contributor.authorNavarro Barea, Natalia
dc.date.accessioned2021-04-22T11:29:00Z
dc.date.available2021-04-22T11:29:00Z
dc.date.issued2017-01-24
dc.identifier.citationAlmazán-Moga A, Zarzosa P, Vidal I, Molist C, Giralt I, Navarro N, et al. Hedgehog Pathway Inhibition Hampers Sphere and Holoclone Formation in Rhabdomyosarcoma. Stem Cells Int. 2017;2017:7507380.
dc.identifier.issn1687-9678
dc.identifier.urihttps://hdl.handle.net/11351/5902
dc.descriptionSoft tissue neoplasms; Hedgehog pathway; Rhabdomyosarcoma
dc.description.abstractRhabdomyosarcoma (RMS) is the most common type of soft tissue sarcoma in children and can be divided into two main subtypes: embryonal (eRMS) and alveolar (aRMS). Among the cellular heterogeneity of tumors, the existence of a small fraction of cells called cancer stem cells (CSC), thought to be responsible for the onset and propagation of cancer, has been demonstrated in some neoplasia. Although the existence of CSC has been reported for eRMS, their existence in aRMS, the most malignant subtype, has not been demonstrated to date. Given the lack of suitable markers to identify this subpopulation in aRMS, we used cancer stem cell-enriched supracellular structures (spheres and holoclones) to study this subpopulation. This strategy allowed us to demonstrate the capacity of both aRMS and eRMS cells to form these structures and retain self-renewal capacity. Furthermore, cells contained in spheres and holoclones showed significant Hedgehog pathway induction, the inhibition of which (pharmacologic or genetic) impairs the formation of both holoclones and spheres. Our findings point to a crucial role of this pathway in the maintenance of these structures and suggest that Hedgehog pathway targeting in CSC may have great potential in preventing local relapses and metastases.
dc.language.isoeng
dc.publisherHindawi
dc.relation.ispartofseriesStem Cells International;2017
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectTumors de parts toves
dc.subjectCèl·lules canceroses
dc.subject.meshRhabdomyosarcoma
dc.subject.meshNeoplastic Stem Cells
dc.subject.meshRhabdomyosarcoma
dc.titleHedgehog Pathway Inhibition Hampers Sphere and Holoclone Formation in Rhabdomyosarcoma
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1155/2017/7507380
dc.subject.decsrabdomiosarcoma
dc.subject.decscélulas madre neoplásicas
dc.subject.decsrabdomiosarcoma
dc.relation.publishversionhttps://www.hindawi.com/journals/sci/2017/7507380/
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Almazán-Moga A, Zarzosa P, Vidal I, Molist C, Giralt I, Navarro N, Soriano A, Segura MF, Roma J] Grup de Recerca translacional en càncer infantil, Vall d'Hebron Institut de Recerca (VHIR), Barcelona, Spain. Vall d'Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Barcelona, Spain. [Sánchez de Toledo J, Gallego S] Grup de Recerca translacional en càncer infantil, Vall d'Hebron Institut de Recerca (VHIR), Barcelona, Spain. Servei d’Oncologia i Hematologia Pediàtriques, Vall d'Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain
dc.identifier.pmid28243259
dc.identifier.wos000394217900001
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/1PN/2008-2011/RD12%2F0036%2F0016
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/2PN/2008-2011/PI11%2F00740
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PE2013-2016/PI14%2F00647
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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