Publicação:
Preclinical anticancer effectiveness of a fraction from Casearia sylvestris and its component Casearin X: in vivo and ex vivo methods and microscopy examinations

dc.contributor.authorPinheiro Ferreira, Paulo Michel
dc.contributor.authorBezerra, Daniel Pereira
dc.contributor.authorSilva, Jurandy do Nascimento
dc.contributor.authorCosta, Marcilia Pinheiro da
dc.contributor.authorOliveira Ferreira, Jose Roberto de
dc.contributor.authorNunes Alencar, Nylane Maria
dc.contributor.authorTavares de Figueiredo, Ingrid Samantha
dc.contributor.authorCavalheiro, Alberto Jose [UNESP]
dc.contributor.authorLongo Machado, Camila Maria [UNESP]
dc.contributor.authorChammas, Roger [UNESP]
dc.contributor.authorNegreiros Nunes Alves, Ana Paula
dc.contributor.authorMoraes, Manoel Odorico de
dc.contributor.authorPessoa, Claudia
dc.contributor.institutionUniv Fed Piaui
dc.contributor.institutionFundacao Oswaldo Cruz
dc.contributor.institutionUniv Fed Ceara
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-11-27T16:55:43Z
dc.date.available2018-11-27T16:55:43Z
dc.date.issued2016-06-20
dc.description.abstractEthnopharmacological relevance: Casearia sylvestris (Salicaceae) is found in South America and presents antiulcerogenic, cytotoxic, antimicrobial, anti-inflammatory and antihypertensive activities. Aim of the study: To assess the in vivo and ex vivo antitumor action of a fraction with casearins (FC) and its main component- Casearin X-isolated from C sylvestris leaves. Materials and methods: Firstly, Sarcoma 180 bearing Swiss mice were treated with FC and Cas X for 7 days. Secondly, BALB/c nude animals received hollow fibers with colon carcinoma (HCT-116) or glioblastoma (SF-295) cells and were treated with FC for 4 days. On 5th day, proliferation was determined by MIT assay. Results: FC 10 and 25 mg/kg/day i.p. and 50 mg/kg/day oral and Cas X 25 mg/kg/day i.p. and 50 mg/kg/ day oral revealed tumor growth inhibition rates of 35.8, 86.2, 53.7, 90.0 and 65.5% and such tumors demonstrated rare mitoses and coagulation necrosis areas. Similarly, FC reduced multiplying of HCT-116 and SF-295 cells when evaluated by the Hollow Fiber Assay (2.5 and 5 mg/kg/day i.p. and 25 and 50 mg/ kg/day oral), with cell growth inhibition rates ranging from 33.3 to 67.4% (p < 0.05). Flow cytometry experiments revealed that FC reduced membrane integrity and induced DNA fragmentation and mitochondrial depolarization (p < 0.05). Conclusions: FC and Cas X were efficient antitumor substances against murine and human cancer cells and caused reversible morphological changes in liver, kidneys and spleens, emphasizing clerodane diterpenes as an emerging class of anticancer molecules. (C) 2016 Elsevier Ireland Ltd. All rights reserved.en
dc.description.affiliationUniv Fed Piaui, Dept Physiol & Biophys, Expt Cancerol Lab, Teresina, Brazil
dc.description.affiliationUniv Fed Piaui, Postgrad Program Pharmaceut Sci, Teresina, Brazil
dc.description.affiliationUniv Fed Piaui, Postgrad Program Biotechnol, Teresina, Brazil
dc.description.affiliationFundacao Oswaldo Cruz, Salvador, BA, Brazil
dc.description.affiliationUniv Fed Piaui, Dept Pharm, Teresina, Brazil
dc.description.affiliationUniv Fed Ceara, Fac Med, Dept Physiol & Pharmacol, Fortaleza, Ceara, Brazil
dc.description.affiliationState Univ Sao Paulo, Inst Chem, Araraquara, Brazil
dc.description.affiliationState Univ Sao Paulo, Ctr Med Nucl, Radioisotopes Res Lab, Sao Paulo, Brazil
dc.description.affiliationState Univ Sao Paulo, Fac Med, Dept Radiol, Sao Paulo, Brazil
dc.description.affiliationUniv Fed Ceara, Dept Clin Odontol, Fortaleza, Ceara, Brazil
dc.description.affiliationFundacao Oswaldo Cruz, Fortaleza, Ceara, Brazil
dc.description.affiliationUnespState Univ Sao Paulo, Inst Chem, Araraquara, Brazil
dc.description.affiliationUnespState Univ Sao Paulo, Ctr Med Nucl, Radioisotopes Res Lab, Sao Paulo, Brazil
dc.description.affiliationUnespState Univ Sao Paulo, Fac Med, Dept Radiol, Sao Paulo, Brazil
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdCNPq: 473167/2012-3
dc.description.sponsorshipIdCNPq: 301976/2013-9
dc.format.extent270-279
dc.identifierhttp://dx.doi.org/10.1016/j.jep.2016.04.011
dc.identifier.citationJournal Of Ethnopharmacology. Clare: Elsevier Ireland Ltd, v. 186, p. 270-279, 2016.
dc.identifier.doi10.1016/j.jep.2016.04.011
dc.identifier.fileWOS000377832000029.pdf
dc.identifier.issn0378-8741
dc.identifier.urihttp://hdl.handle.net/11449/165207
dc.identifier.wosWOS:000377832000029
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofJournal Of Ethnopharmacology
dc.relation.ispartofsjr1,150
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.subjectCasearin X
dc.subjectHollow fiber assay
dc.subjectSarcoma 180
dc.subjectAntineoplastic
dc.subjectLeukogram
dc.subjectToxicity
dc.titlePreclinical anticancer effectiveness of a fraction from Casearia sylvestris and its component Casearin X: in vivo and ex vivo methods and microscopy examinationsen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
unesp.author.lattes2518006820764120[8]
unesp.author.orcid0000-0001-6862-6497[1]
unesp.author.orcid0000-0003-0342-8726[10]
unesp.author.orcid0000-0001-8214-9957[8]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Química, Araraquarapt
unesp.departmentQuímica Orgânica - IQARpt

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