Morphological and biochemical alterations activated by antitumor clerodane diterpenes

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 [UNESP]
dc.contributor.authorCavalheiro, Alberto José [UNESP]
dc.contributor.authorBolzani, Vanderlan da Silva [UNESP]
dc.contributor.authorSiqueira Silva, Dulce Helena [UNESP]
dc.contributor.authorPessoa, Claudia
dc.contributor.institutionUniv Fed Piaui
dc.contributor.institutionUniversidade Federal de Pernambuco (UFPE)
dc.contributor.institutionUniv Fed Ceara
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2015-03-18T15:53:21Z
dc.date.available2015-03-18T15:53:21Z
dc.date.issued2014-10-05
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.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.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.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.doi10.1016/j.cbi.2014.10.015
dc.identifier.issn0009-2797
dc.identifier.lattes2518006820764120
dc.identifier.lattes4484083685251673
dc.identifier.lattes4702004904231248
dc.identifier.urihttp://hdl.handle.net/11449/116465
dc.identifier.wosWOS:000346461800014
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofChemico-biological Interactions
dc.relation.ispartofjcr3.296
dc.relation.ispartofsjr1,033
dc.rights.accessRightsAcesso restrito
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.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
unesp.author.lattes2518006820764120[7]
unesp.author.lattes4484083685251673
unesp.author.lattes4702004904231248
unesp.author.lattes4000625974516852[6]
unesp.author.orcid0000-0002-4920-2506[6]
unesp.author.orcid0000-0001-8214-9957[7]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Química, Araraquarapt
unesp.departmentQuímica Orgânica - IQARpt

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