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dc.contributor.authorPavon, Lorena Favaro-
dc.contributor.authorSibov, Tatiana Tais-
dc.contributor.authorOliveira, Daniela Mara de-
dc.contributor.authorMarti, Luciana C.-
dc.contributor.authorCabral, Francisco Romero-
dc.contributor.authorSouza, Jean Gabriel de-
dc.contributor.authorBoufleur, Pamela-
dc.contributor.authorMalheiros, Suzana M. F.-
dc.contributor.authorNeto, Manuel A. de Paiva-
dc.contributor.authorCruz, Edgard Ferreira da-
dc.contributor.authorTavassi, Ana Marisa Chudzinski-
dc.contributor.authorCavalheiro, Sérgio-
dc.date.accessioned2018-12-11T11:01:30Z-
dc.date.available2018-12-11T11:01:30Z-
dc.date.issued2016-05-
dc.identifier.citationPAVON, Lorena Favaro et al. Mesenchymal stem cell-like properties of CD133+ glioblastoma initiating cells. Oncotarget, Nova York, v. 7, p. 40546-40557, maio 2016. DOI: https://doi.org/10.18632/oncotarget.9658. Disponível em: http://www.impactjournals.com/oncotarget/index.php?journal=oncotarget&page=article&op=view&path[]=9658&path[]=41659. Acesso em: 11 dez. 2018.pt_BR
dc.identifier.urihttp://repositorio.unb.br/handle/10482/33159-
dc.language.isoInglêspt_BR
dc.publisherImpact Journalspt_BR
dc.rightsAcesso Abertopt_BR
dc.titleMesenchymal stem cell-like properties of CD133+ glioblastoma initiating cellspt_BR
dc.typeArtigopt_BR
dc.subject.keywordNeurosferaspt_BR
dc.subject.keywordGlicoproteínaspt_BR
dc.subject.keywordCélulas-troncopt_BR
dc.subject.keywordMicroscopia eletrônicapt_BR
dc.subject.keywordTumorespt_BR
dc.rights.licenseOncotarget - All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 License (CC BY). Fonte: http://www.oncotarget.com/index.php?journal=oncotarget&page=article&op=view&path[]=9658&path[]=41659. Acesso em: 11 dez. 2018.pt_BR
dc.identifier.doihttps://doi.org/10.18632/oncotarget.9658pt_BR
dc.description.abstract1Glioblastoma is composed of dividing tumor cells, stromal cells and tumor initiating CD133+ cells. Recent reports have discussed the origin of the glioblastoma CD133+ cells and their function in the tumor microenvironment. The present work sought to investigate the multipotent and mesenchymal properties of primary highly purified human CD133+ glioblastoma-initiating cells. To accomplish this aim, we used the following approaches: i) generation of tumor subspheres of CD133+ selected cells from primary cell cultures of glioblastoma; ii) analysis of the expression of pluripotency stem cell markers and mesenchymal stem cell (MSC) markers in the CD133+ glioblastoma-initiating cells; iii) side-by-side ultrastructural characterization of the CD133+ glioblastoma cells, MSC and CD133+ hematopoietic stem cells isolated from human umbilical cord blood (UCB); iv) assessment of adipogenic differentiation of CD133+ glioblastoma cells to test their MSC-like in vitro differentiation ability; and v) use of an orthotopic glioblastoma xenograft model in the absence of immune suppression. We found that the CD133+ glioblastoma cells expressed both the pluripotency stem cell markers (Nanog, Mush-1 and SSEA-3) and MSC markers. In addition, the CD133+ cells were able to differentiate into adipocyte-like cells. Transmission electron microscopy (TEM) demonstrated that the CD133+ glioblastoma-initiating cells had ultrastructural features similar to those of undifferentiated MSCs. In addition, when administered in vivo to non-immunocompromised animals, the CD133+ cells were also able to mimic the phenotype of the original patient’s tumor. In summary, we showed that the CD133+ glioblastoma cells express molecular signatures of MSCs, neural stem cells and pluripotent stem cells, thus possibly enabling differentiation into both neural and mesodermal cell types.pt_BR
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