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Antitumor activity of Kielmeyera coriacea leaf constituents in experimental melanoma, tested in vitro and in vivo in syngeneic mice

dc.contributor.authorFigueiredo, Carlos Rogério de
dc.contributor.authorMatsuo, Alisson Leonardo
dc.contributor.authorMassaoka, Mariana Hiromi
dc.contributor.authorGirola, Natália
dc.contributor.authorAzevedo, Ricardo Alexandre
dc.contributor.authorRabaça, Aline Nogueira
dc.contributor.authorFarias, Camyla Fernandes
dc.contributor.authorPereira, Felipe Valença
dc.contributor.authorMatias, Natália Silva [UNESP]
dc.contributor.authorSilva, Luciana Pereira [UNESP]
dc.contributor.authorRodrigues, Elaine Guadelupe
dc.contributor.authorLago, João Henrique Guilardi
dc.contributor.authorTravassos, Luiz Rodolpho
dc.contributor.authorSilva, Regildo Márcio Gonçalves da [UNESP]
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T16:56:31Z
dc.date.accessioned2015-05-15T13:30:28Z
dc.date.available2018-12-11T16:56:31Z
dc.date.available2015-05-15T13:30:28Z
dc.date.issued2014
dc.description.abstractPurpose: The antitumor activity of Kielmeyera coriacea (Clusiaceae), a medicinal plant used in the treatment of parasitic, as well as fungal and bacterial infections by the Brazilian Cerrado population, was investigated. Methods: A chloroform extract (CE) of K. coriacea was tested in the murine melanoma cell line (B16F10-Nex2) and a panel of human tumor cell lines. Tumor cell migration was determined by the wound-healing assay and the in vivo antitumor activity of CE was investigated in a melanoma cell metastatic model. 1H NMR and GC/MS were used to determine CE chemical composition. Results: We found that CE exhibited strong cytotoxic activity against murine melanoma cells and a panel of human tumor cell lines in vitro. CE also inhibited growth of B16F10- Nex2 cells at sub lethal concentrations, inducing cell cycle arrest at S phase, and inhibition of tumor cell migration. Most importantly, administration of CE significantly reduced the number of melanoma metastatic nodules in vivo. Chemical analysis of CE indicated the presence of the long chain fatty compounds, 1-eicosanol, 1-docosanol, and 2-nonadecanone as main constituents. Conclusion: These results indicate that K. coriacea is a promising medicinal plant in cancer therapy exhibiting antitumor activity both in vitro and in vivo against different tumor cell lines.en
dc.description.affiliationDepartment of Microbiology Immunology and Parasitology Experimental Oncology Unit (UNONEX) Federal University of São Paulo (UNIFESP), São Paulo
dc.description.affiliationDepartment of Biological Sciences - Laboratory of Herbal Medicines Universidade Estadual Paulista (UNESP- FLC/Assis), São Paulo
dc.description.affiliationInstitute of Environmental Chemical and Pharmaceutical Sciences Federal University of São Paulo (UNIFESP), Diadema, São Paulo, SP
dc.description.affiliationUnespUniversidade Estadual Paulista Júlio de Mesquita Filho, Faculdade de Ciências e Letras de Assis, Assis, Avenida Dom Antonio, 2100, Vila Universitária, CEP 19806-900, SP, Brasil
dc.format.extent429-436
dc.identifierhttp://dx.doi.org/10.5681/apb.2014.063
dc.identifier.citationAdvanced Pharmaceutical Bulletin, v. 4, n. 1, p. 429-436, 2014.
dc.identifier.doi10.5681/apb.2014.063
dc.identifier.fileISSN2251-7308-2014-04-01-429-436.pdf
dc.identifier.issn2251-7308
dc.identifier.issn2228-5881
dc.identifier.lattes5285324361162578
dc.identifier.lattes8207280726883591
dc.identifier.orcid0000-0002-0300-0247
dc.identifier.scopus2-s2.0-84906778194
dc.identifier.urihttp://hdl.handle.net/11449/181813
dc.language.isoeng
dc.relation.ispartofAdvanced Pharmaceutical Bulletin
dc.relation.ispartofsjr0,632
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.sourceCurrículo Lattes
dc.subjectAnti-tumor
dc.subjectCancer
dc.subjectCell cycle arrest
dc.subjectCell migration
dc.subjectCerrado
dc.subjectCytotoxic
dc.titleAntitumor activity of Kielmeyera coriacea leaf constituents in experimental melanoma, tested in vitro and in vivo in syngeneic miceen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublication4a016e93-a452-4c24-b800-ecc2ea22a1fd
relation.isDepartmentOfPublication.latestForDiscovery4a016e93-a452-4c24-b800-ecc2ea22a1fd
relation.isOrgUnitOfPublicationc3f68528-5ea8-4b32-a9f4-3cfbd4bba64d
relation.isOrgUnitOfPublication.latestForDiscoveryc3f68528-5ea8-4b32-a9f4-3cfbd4bba64d
unesp.author.lattes5285324361162578[14]
unesp.author.lattes8207280726883591
unesp.author.orcid0000-0002-0300-0247[14]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências e Letras, Assispt
unesp.departmentCiências Biológicas - FCLASpt

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