Antitumor effect of cell therapy with mesenchymal stem cells on murine melanoma B16-F10
dc.contributor | Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP | |
dc.contributor.author | MENEZES, Fernanda Carrilho de | |
dc.contributor.author | CABRAL, Laertty Garcia de Sousa | |
dc.contributor.author | PETRELLIS, Maria Carla | |
dc.contributor.author | FESTA NETO, Cyro | |
dc.contributor.author | MARIA, Durvanei Augusto | |
dc.date.accessioned | 2020-10-15T14:33:07Z | |
dc.date.available | 2020-10-15T14:33:07Z | |
dc.date.issued | 2020 | |
dc.description.abstract | In 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 GO/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. | eng |
dc.description.index | MEDLINE | eng |
dc.description.sponsorship | CNPqNational Council for Scientific and Technological Development (CNPq) [306124/2015-7] | |
dc.identifier.citation | BIOMEDICINE & PHARMACOTHERAPY, v.128, article ID 110294, 12p, 2020 | |
dc.identifier.doi | 10.1016/j.biopha.2020.110294 | |
dc.identifier.eissn | 1950-6007 | |
dc.identifier.issn | 0753-3322 | |
dc.identifier.uri | https://observatorio.fm.usp.br/handle/OPI/37721 | |
dc.language.iso | eng | |
dc.publisher | ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER | eng |
dc.relation.ispartof | Biomedicine & Pharmacotherapy | |
dc.rights | openAccess | eng |
dc.rights.holder | Copyright ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER | eng |
dc.subject | Tumor | eng |
dc.subject | Melanoma | eng |
dc.subject | Mesenchymal stem cells | eng |
dc.subject | Immunomodulatory | eng |
dc.subject | Apoptosis | eng |
dc.subject.other | cutaneous melanoma | eng |
dc.subject.other | angiogenesis | eng |
dc.subject.other | delivery | eng |
dc.subject.other | strategy | eng |
dc.subject.wos | Medicine, Research & Experimental | eng |
dc.subject.wos | Pharmacology & Pharmacy | eng |
dc.title | Antitumor effect of cell therapy with mesenchymal stem cells on murine melanoma B16-F10 | eng |
dc.type | article | eng |
dc.type.category | original article | eng |
dc.type.version | publishedVersion | eng |
dspace.entity.type | Publication | |
hcfmusp.author.external | CABRAL, Laertty Garcia de Sousa:Butantan Inst, Mol Biol Lab, Av Dr Vital Brasil 1500, BR-05599000 Sao Paulo, Brazil | |
hcfmusp.author.external | PETRELLIS, Maria Carla:Butantan Inst, Mol Biol Lab, Av Dr Vital Brasil 1500, BR-05599000 Sao Paulo, Brazil | |
hcfmusp.author.external | MARIA, Durvanei Augusto:Butantan Inst, Mol Biol Lab, Av Dr Vital Brasil 1500, BR-05599000 Sao Paulo, Brazil | |
hcfmusp.citation.scopus | 3 | |
hcfmusp.contributor.author-fmusphc | FERNANDA CARRILHO DE MENEZES | |
hcfmusp.contributor.author-fmusphc | CYRO FESTA NETO | |
hcfmusp.description.articlenumber | 110294 | |
hcfmusp.description.volume | 128 | |
hcfmusp.origem | WOS | |
hcfmusp.origem.pubmed | 32485571 | |
hcfmusp.origem.scopus | 2-s2.0-85085571633 | |
hcfmusp.origem.wos | WOS:000561739400007 | |
hcfmusp.publisher.city | ISSY-LES-MOULINEAUX | eng |
hcfmusp.publisher.country | FRANCE | eng |
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hcfmusp.scopus.lastupdate | 2024-05-10 | |
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relation.isAuthorOfPublication | 02795968-5c04-4c21-863d-e11038aba5b8 | |
relation.isAuthorOfPublication.latestForDiscovery | dfc3734a-a125-4997-9406-5db312e21417 |
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