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Antitumor activity of extracts from Peperomia elongata

dc.contributor.authorde Castro Campos, Patricia Bonavides
dc.contributor.authorTorres Gama, Juliana Julian [UNESP]
dc.contributor.authorPereira, Licia Pacheco
dc.contributor.authorCosta-Lotufo, Leticia Veras
dc.contributor.authorde Moraes, Manoel Odorico
dc.contributor.authorGuimaraes, Elsie Franklin
dc.contributor.authorKato, Massuo Jorge
dc.contributor.authorFurlan, Maysa [UNESP]
dc.contributor.authorPessoa, Claudia
dc.contributor.institutionUniversidade Federal do Ceará (UFC)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionInst Pesquisas Jardim Bot Rio de Janeiro
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-20T15:27:34Z
dc.date.available2014-05-20T15:27:34Z
dc.date.issued2007-01-01
dc.description.abstractThe cytotoxic potential of ethanol extracts from Peperomia elongata H. B. & K. (Piperaceae) were evaluated against human cancer cell lines by the MTT method. The samples considered cytotoxic were tested for antimitotic activity with the sea urchin egg development test and for hemolytic activity using mice erythrocytes. The extracts from leaves (hexane), stems (ethanol, hexane, hexane: AcOEt, AcOEt, and MeOH: H2O insoluble), and roots (R4) presented potential cytotoxic action. The stems extracts showed the highest toxicity in all tumor cell lines tested, with an IC50 <= 9.0 mu g/mL for ethanol extract, IC50 <= 11.6 mu g/mL for MeOH:H2O insoluble, IC50 <= 7.3 mu g/mL for hexane extract, IC50 <= 11.4 mu g/mL for hexane: AcOEt, and IC50 <= 16.2 mu g/mL for AcOEt extract. All extracts considered cytotoxic for tumoral cell lines presented antimitotic activity. The samples from roots (R4) and stems (ethanol, MeOH: H2O insoluble, and hexane extract from leaves) were found to possess lytic activity in mice erythrocytes but in higher doses (> 125 mu g/mL). Further studies for the isolation and identification of the active principles of these extracts should be undertaken.en
dc.description.affiliationUniv Fed Ceara, Expt Oncol Lab, Fortaleza, Ceara, Brazil
dc.description.affiliationUniv Estadual Paulista, Inst Quim, Araraquara, SP, Brazil
dc.description.affiliationInst Pesquisas Jardim Bot Rio de Janeiro, Rio de Janeiro, Brazil
dc.description.affiliationUniv São Paulo, Inst Quim, São Paulo, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Inst Quim, Araraquara, SP, Brazil
dc.format.extent760-765
dc.identifierhttp://dx.doi.org/10.1080/13880200701585857
dc.identifier.citationPharmaceutical Biology. Philadelphia: Taylor & Francis Inc., v. 45, n. 10, p. 760-765, 2007.
dc.identifier.doi10.1080/13880200701585857
dc.identifier.issn1388-0209
dc.identifier.lattes1308042794786872
dc.identifier.urihttp://hdl.handle.net/11449/37519
dc.identifier.wosWOS:000251972600006
dc.language.isoeng
dc.publisherTaylor & Francis Inc
dc.relation.ispartofPharmaceutical Biology
dc.relation.ispartofjcr1.918
dc.relation.ispartofsjr0,563
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectantitumorpt
dc.subjectcytotoxic activitypt
dc.subjectMTT assaypt
dc.subjectPeperomiapt
dc.subjectpiperaceaept
dc.titleAntitumor activity of extracts from Peperomia elongataen
dc.typeArtigopt
dcterms.licensehttp://journalauthors.tandf.co.uk/permissions/reusingOwnWork.asp
dcterms.rightsHolderTaylor & Francis Inc
dspace.entity.typePublication
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscoverybc74a1ce-4c4c-4dad-8378-83962d76c4fd
unesp.author.lattes1308042794786872
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentQuímica Orgânica - IQARpt

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