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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/116465
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dc.contributor.authorPinheiro Ferreira, Paulo Michel-
dc.contributor.authorGadelha Militao, Gardenia Carmen-
dc.contributor.authorBarbosa Lima, Daisy Jereissati-
dc.contributor.authorJesus Costa, Nagilla Daniela de-
dc.contributor.authorMachado, Katia da Conceicao-
dc.contributor.authorSantos, Andre Gonzaga dos-
dc.contributor.authorCavalheiro, Alberto José-
dc.contributor.authorBolzani, Vanderlan da Silva-
dc.contributor.authorSiqueira Silva, Dulce Helena-
dc.contributor.authorPessoa, Claudia-
dc.date.accessioned2015-03-18T15:53:21Z-
dc.date.accessioned2016-10-25T20:24:51Z-
dc.date.available2015-03-18T15:53:21Z-
dc.date.available2016-10-25T20:24:51Z-
dc.date.issued2014-10-05-
dc.identifierhttp://dx.doi.org/10.1016/j.cbi.2014.10.015-
dc.identifier.citationChemico-biological Interactions. Clare: Elsevier Ireland Ltd, v. 222, p. 112-125, 2014.-
dc.identifier.issn0009-2797-
dc.identifier.urihttp://hdl.handle.net/11449/116465-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/116465-
dc.description.abstractCasearia sylvestris Swartz (Salicaceae) is a plant commonly widespread in the Americas. It has oxygenated tricyclic bioactive clerodane diterpenes with antimicrobial, antiulcer, larvicidal, chemopreventive, anti-inflammatory, antioxidant and antiproliferative properties. Due to this requirement for the developing of new anticancer drugs, it was initially evaluated the cytotoxic activity of a fraction with Casearins (FC) and its clerodane diterpenes Casearin B (Cas B), D (Cas D), X (Cas X) and Caseargrewiin F (Cas F) isolated from C. sylvestris leaves against 7 tumor cell lines, Sarcoma 180 cells (S180) and on normal peripheral blood mononuclear cells (PBMC). All substances tested showed cytotoxic potential. Cas F and X were the most active compounds. Cell death analyzes with Cas F (0.5 and 1 mu M) and Cas X (0.7 and 1.5 mu M) using the HL-60 leukemia line as experimental model showed DNA synthesis and membrane integrity reduction, DNA fragmentation and mitochondrial depolarization, specially after 24 h exposure, cell cycle arrest in G(0)/G(1) phase caused by Cas X, activation of the initiator -8/-9 and effector -3/-7 caspases and phosphatidylserine externalization, all biochemical features of apoptosis corroborated by chromatinic condensation, karyorrhexis, cytoplasmic vacuolation and rarefaction and cellular shrinkage, morphological findings specially observed after 12 and 24 h of incubation. Therefore, Cas X and F were the most functional molecules with more pronounced lethal and discriminating effects on tumor cells and antiproliferative action predominantly mediated by apoptosis, highlighting clerodane dipertenes as promising lead antineoplastic compounds. (C) 2014 Elsevier Ireland Ltd. All rights reserved.en
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.description.sponsorshipBrazilian agency Fundacao Cearense de Apoio ao Desenvolvimento Cientifico e Tecnologico (FUNCAP)-
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipBrazilian agency Fundacao de Amparo a Pesquisa do Estado do Piaui (FAPEPI)-
dc.format.extent112-125-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectCasearia sylvestrisen
dc.subjectCytotoxicityen
dc.subjectAntiproliferative actionen
dc.subjectApoptosisen
dc.subjectHuman cellsen
dc.subjectMurine cellsen
dc.titleMorphological and biochemical alterations activated by antitumor clerodane diterpenesen
dc.typeoutro-
dc.contributor.institutionUniv Fed Piaui-
dc.contributor.institutionUniversidade Federal de Pernambuco (UFPE)-
dc.contributor.institutionUniv Fed Ceara-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUniv Fed Piaui, Dept Physiol & Biophys, Teresina, Brazil-
dc.description.affiliationUniv Fed Piaui, Postgrad Program Pharmaceut Sci, Teresina, Brazil-
dc.description.affiliationUniv Fed Pernambuco, Dept Physiol & Pharmacol, Recife, PE, Brazil-
dc.description.affiliationUniv Fed Piaui, Dept Biol Sci, Picos, Brazil-
dc.description.affiliationUniv Fed Ceara, Dept Physiol & Pharmacol, Fortaleza, Ceara, Brazil-
dc.description.affiliationState Univ Sao Paulo Julio Mesquita Filho, Fac Pharmaceut Sci, Araraquara, Brazil-
dc.description.affiliationState Univ Sao Paulo Julio Mesquita Filho, Inst Chem, Araraquara, Brazil-
dc.description.affiliationUnespState Univ Sao Paulo Julio Mesquita Filho, Fac Pharmaceut Sci, Araraquara, Brazil-
dc.description.affiliationUnespState Univ Sao Paulo Julio Mesquita Filho, Inst Chem, Araraquara, Brazil-
dc.identifier.doi10.1016/j.cbi.2014.10.015-
dc.identifier.wosWOS:000346461800014-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofChemico-biological Interactions-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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