Publication:
Role of Activator Protein-1 Complex on the Phenotype of Human Osteosarcomas Generated from Mesenchymal Stem Cells

dc.contributor.authorGambera, Stefano
dc.contributor.authorAbarrategi, Ander
dc.contributor.authorRodriguez-Milla, Miguel A
dc.contributor.authorMulero, Francisca
dc.contributor.authorMenéndez, Sofía T
dc.contributor.authorRodriguez, Rene
dc.contributor.authorNavarro, Samuel
dc.contributor.authorGarcia-Castro, Javier
dc.contributor.funderInstituto de Salud Carlos III
dc.contributor.funderCentro de Investigación Biomédica en Red - CIBERONC (Cáncer)
dc.contributor.funderAgencia Estatal de Investigación (España)
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)
dc.contributor.funderComunidad de Madrid (España)
dc.contributor.funderRed Temática de Investigación Cooperativa en Cáncer (RTICC) (España)
dc.date.accessioned2023-02-28T10:45:56Z
dc.date.available2023-02-28T10:45:56Z
dc.date.issued2018-10
dc.description.abstractOsteosarcoma (OS) is a highly aggressive bone tumor that usually arises intramedullary at the extremities of long bones. Due to the fact that the peak of incidence is in the growth spurt of adolescence, the specific anatomical location, and the heterogeneity of cells, it is believed that osteosarcomagenesis is a process associated with bone development. Different studies in murine models showed that the tumor-initiating cell in OS could be an uncommitted mesenchymal stem cell (MSC) developing in a specific bone microenvironment. However, only a few studies have reported transgene-induced human MSCs transformation and mostly obtained undifferentiated sarcomas. In our study, we demonstrate that activator protein 1 family members induce osteosarcomagenesis in immortalized hMSC. c-JUN or c-JUN/c-FOS overexpression act as tumorigenic factors generating OS with fibroblastic or pleomorphic osteoblastic phenotypes, respectively. Stem Cells 2018;36:1487-1500.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThis work was supported by grants from the Fondo de Investigaciones Sanitarias (FIS: PI11/00377 [to J.G.-C.]; and RTICC: RD12/0036/0027 [to J.G.-C.], RD12/0036/0020 [to S.N.]; Consorcio CIBERONC CB16/12/00390 [to R.R.] and CB16/12/00484 [to S.N.]; Miguel Servet II Program CPII16/00049 [to R.R.]; and Sara Borrell CD16/13/00103 [to S.T.M.] and CD11/00132 [to A.A.]); The Juan de la Cierva program JCI2010-06123 [to A.A]); the Agencia Estatal de Investigación (AEI) (MINECO/Fondo Europeo de Desarrollo Regional [FEDER]: SAF2016-75286-R [to R.R.]); and the Madrid Regional Government (CellCAM; P2010/BMD-2420 [to J.G.-C.]) in Spain.es_ES
dc.format.number10es_ES
dc.format.page1487-1500es_ES
dc.format.volume36es_ES
dc.identifier.citationStem Cells. 2018 Oct;36(10):1487-1500.es_ES
dc.identifier.doi10.1002/stem.2869es_ES
dc.identifier.e-issn1549-4918es_ES
dc.identifier.journalStem cells (Dayton, Ohio)es_ES
dc.identifier.pubmedID30001480es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/15550
dc.language.isoenges_ES
dc.publisherOxford University Press
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/MINECO//RD12%2F0036%2F0020/ES/Cáncer/es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/MINECO//RD12%2F0036%2F0027/ES/Cáncer/es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/MINECO//CB16%2F12%2F00390/ES/CANCER/es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/MINECO//CB16%2F12%2F00484/ES/CANCER/es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/MINECO//CPII16%2F00049/ES/CPII16%2F00049/es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/SAF2016-75286-Res_ES
dc.relation.projectFISinfo:fis/Instituto de Salud Carlos III/null/null/Subprograma de proyectos de investigacion en salud (AES 2011) (2011)/PI11/00377es_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/CD16/13/00103es_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/CD11/00132es_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/JCI2010-06123es_ES
dc.relation.publisherversionhttps://doi.org/10.1002/stem.2869es_ES
dc.repisalud.centroISCIII::Instituto de Investigación de Enfermedades Rarases_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectMesenchymal stem cellses_ES
dc.subjectOsteosarcomaes_ES
dc.subjectp53es_ES
dc.subjectRbc-JUNes_ES
dc.subjectc-FOSes_ES
dc.subject.meshAnimalses_ES
dc.subject.meshBone Neoplasmses_ES
dc.subject.meshHeterograftses_ES
dc.subject.meshHumanses_ES
dc.subject.meshMesenchymal Stem Cellses_ES
dc.subject.meshMicees_ES
dc.subject.meshMice, SCIDes_ES
dc.subject.meshOsteosarcomaes_ES
dc.subject.meshPhenotypees_ES
dc.subject.meshTranscription Factor AP-1es_ES
dc.titleRole of Activator Protein-1 Complex on the Phenotype of Human Osteosarcomas Generated from Mesenchymal Stem Cellses_ES
dc.typeresearch articlees_ES
dc.type.hasVersionVoRes_ES
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