Antitumor effect of cell therapy with mesenchymal stem cells on murine melanoma B16-F10

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dc.contributorLaboratório de Biologia Molecularpt_BR
dc.contributor.authorMenezes, Fernanda Carrilho dept_BR
dc.contributor.authorCabral, Laertty Garcia de Sousapt_BR
dc.contributor.authorPetrellis, Maria Carlapt_BR
dc.contributor.authorFesta Neto, Cyropt_BR
dc.contributor.authorMaria, Durvanei Augustopt_BR
dc.date.accessioned2020-07-09T21:27:57Z-
dc.date.available2020-07-09T21:27:57Z-
dc.date.issued2020-
dc.identifier.citationMenezes FC, Cabral LGS, Petrellis MC, Festa Neto C, Maria DA. Antitumor effect of cell therapy with mesenchymal stem cells on murine melanoma B16-F10. Biomed. Pharmacother.. 2020 Aug;128:110294. doi:10.1016/j.biopha.2020.110294.pt_BR
dc.identifier.issn0753-3322-
dc.identifier.issn1950-6007-
dc.identifier.urihttps://repositorio.butantan.gov.br/handle/butantan/3054-
dc.description.abstractIn this study, the antitumor and immunomodulatory effects of mesenchymal stem cells (MSC) obtained from bone marrow in the treatment of dorsal melanoma B16-F10. The MSC cells were obtained from the bone marrow of isogenic C57BL/6J mice, characterized and inoculated by two routes, intratumor (it) and intravenous (iv). The hematological profile, expression markers and receptors, phases of the cell cycle and mitochondrial electrical potential were evaluated by flow cytometry. The dorsal tumor mass showed a significant reduction after treatment by the two routes of administration with a significant effect by the intravenous route. MSC showed immunomodulatory potential and did not induce an increase in the markers involved in tumor control and progression. The number of cells in the sub-G1 phase increased significantly after treatments compared to the control group. The percentage of cells in phases G0/G1, S and G2/M decreased, with only the group (it) showing a significant reduction. The intratumor group showed a significant decrease in the G2/M phase. Treatment with MSC provided a significant decrease in the percentage of metabolically active tumor cells, demonstrating its intrinsic effect in the control of cell proliferation. Regarding the mechanism of cell death, MSCs modulated the expression of proteins involved in the regulation of the cell cycle, angiogenesis receptors and pro-apoptotic proteins by intrinsic and extrinsic routes. Therefore, the use of undifferentiated MSC, administered intratumor and intravenous is possibly a promising treatment for melanoma.pt_BR
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)pt_BR
dc.format.extent110294pt_BR
dc.languageengpt_BR
dc.publisherEditions Scientifiques Elsevierpt_BR
dc.relation.ispartofBiomedicine & Pharmacotherapypt_BR
dc.rightsOpen Accesspt_BR
dc.titleAntitumor effect of cell therapy with mesenchymal stem cells on murine melanoma B16-F10pt_BR
dc.typeArticlept_BR
dc.identifier.doi10.1016/j.biopha.2020.110294pt_BR
dc.identifier.urlhttps://doi.org/10.1016/j.biopha.2020.110294pt_BR
dc.contributor.externalUniversidade de São Paulo (USP)¦¦Brasilpt_BR
dc.publisher.cityParispt_BR
dc.identifier.citationvolume128pt_BR
dc.subject.keywordTumorpt_BR
dc.subject.keywordMelanomapt_BR
dc.subject.keywordMesenchymal stem cellspt_BR
dc.subject.keywordImmunomodulatorypt_BR
dc.subject.keywordApoptosispt_BR
dc.relation.ispartofabbreviatedBiomed. Pharmacother.pt_BR
dc.identifier.citationabntv. 128, 110294, ago. 2020pt_BR
dc.identifier.citationvancouver2020 Aug;128:110294pt_BR
dc.publisher.countryFrancept_BR
dc.contributor.butantanCabral, Laertty Garcia de Sousa|:Aluno|:Laboratório de Biologia Molecular|:pt_BR
dc.contributor.butantanPetrellis, Maria Carla|:Aluno|:Laboratório de Biologia Molecular|:pt_BR
dc.contributor.butantanMaria, Durvanei Augusto|:Pesquisador|:Laboratório de Biologia Molecular|:Autor de correspondênciapt_BR
dc.sponsorship.butantanConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)¦¦306124/2015-7pt_BR
dc.identifier.bvsccBR78.1pt_BR
dc.identifier.bvsdbIBProdpt_BR
item.openairetypeArticle-
item.fulltextCom Texto completo-
item.grantfulltextembargo_29990101-
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