Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/1577
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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP-
dc.contributor.authorKONAN, Nzi Andre-
dc.contributor.authorLINCOPAN, Nilton-
dc.contributor.authorDIAZ, Ingrit Elida Collantes-
dc.contributor.authorJACYSYN, Jacqueline de Fatima-
dc.contributor.authorTIBA, Mirtes Midori Tanae-
dc.contributor.authorMENDES, Joao Gustavo Pessini Amarante-
dc.contributor.authorBACCHI, Elfriede Marianne-
dc.contributor.authorSPIRA, Beny-
dc.date.accessioned2013-07-30T17:53:38Z-
dc.date.available2013-07-30T17:53:38Z-
dc.date.issued2012-
dc.identifier.citationEXPERIMENTAL AND TOXICOLOGIC PATHOLOGY, v.64, n.5, p.435-440, 2012-
dc.identifier.issn0940-2993-
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/1577-
dc.description.abstractThe leaves of the Cashew plant (Anacardium occidentale L.) are used by the folk medicine in South America and West Africa. This plant is rich in flavonoids, which are polyphenolic compounds widespread in plants, and that have diverse physiological effects. In a sub-acute toxicity assay it was found that an ethanolic extract of Cashew leaves elicited lymphopenia in rats. The extract was also found to be cytotoxic and to induce apoptosis in Jurkat (acute lymphoblastic leukemia) cells. The crude ethanolic extract was fractionated and resolved by HPLC. One of the four fractions obtained led to the isolation of the biflavonoid agasthisflavone. [H-3]-thymidine incorporation assays and flow cytometry analysis showed that the isolated compound displayed a high anti-proliferative effect in Jurkat cells with an IC50 of 2.4 mu g/ml (4.45 mu M). The effect of agathisflavone on the acute promyelocytic leukemia cell line HL60, Burkitt lymphoma Raji cells and Hep-2 laryngeal carcinoma cells was also tested. The two latter ones were only mildly affected by agathisflavone. It is also shown that agathisflavone induces apoptosis in Jurkat cells and it this proposed that this is the likely mechanism of agathisflavone specific cytotoxicity.-
dc.description.sponsorshipBryan Gunn's Leukaemia Appeal (UK)-
dc.language.isoeng-
dc.publisherELSEVIER GMBH, URBAN & FISCHER VERLAG-
dc.relation.ispartofExperimental and Toxicologic Pathology-
dc.rightsrestrictedAccess-
dc.subjectCashew-
dc.subjectRats-
dc.subjectLeukemia cells-
dc.subject.otherchronic lymphocytic-leukemia-
dc.subject.othert-cells-
dc.subject.otherphosphodiesterases-
dc.subject.otherbiflavonoids-
dc.subject.otherapoptosis-
dc.subject.otheractivation-
dc.subject.otherinhibitors-
dc.subject.othertoxicity-
dc.subject.otherproteins-
dc.subject.otherextract-
dc.titleCytotoxicity of cashew flavonoids towards malignant cell lines-
dc.typearticle-
dc.rights.holderCopyright ELSEVIER GMBH, URBAN & FISCHER VERLAG-
dc.identifier.doi10.1016/j.etp.2010.10.010-
dc.identifier.pmid21106357-
dc.subject.wosPathology-
dc.subject.wosToxicology-
dc.type.categoryoriginal article-
dc.type.versionpublishedVersion-
hcfmusp.author.externalKONAN, Nzi Andre:Univ Sao Paulo, Inst Ciencias Biomed, Dept Microbiol, BR-05508 Sao Paulo, Brazil-
hcfmusp.author.externalLINCOPAN, Nilton:Univ Sao Paulo, Inst Ciencias Biomed, Dept Microbiol, BR-05508 Sao Paulo, Brazil-
hcfmusp.author.externalDIAZ, Ingrit Elida Collantes:Univ Sao Paulo, Inst Quim, Dept Quim Organ, Sao Paulo, Brazil-
hcfmusp.author.externalTIBA, Mirtes Midori Tanae:Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Farmacol, Sao Paulo, Brazil-
hcfmusp.author.externalMENDES, Joao Gustavo Pessini Amarante:Univ Sao Paulo, Inst Ciencias Biomed, Dept Imunol, BR-05508 Sao Paulo, Brazil-
hcfmusp.author.externalBACCHI, Elfriede Marianne:Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Farmacol, Sao Paulo, Brazil-
hcfmusp.author.externalSPIRA, Beny:Univ Sao Paulo, Inst Ciencias Biomed, Dept Microbiol, BR-05508 Sao Paulo, Brazil-
hcfmusp.description.beginpage435-
hcfmusp.description.endpage440-
hcfmusp.description.issue5-
hcfmusp.description.volume64-
hcfmusp.origemWOS-
hcfmusp.origem.idWOS:000304513300006-
hcfmusp.origem.id2-s2.0-84860455346-
hcfmusp.publisher.cityJENA-
hcfmusp.publisher.countryGERMANY-
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dc.description.indexMEDLINE-
hcfmusp.citation.scopus41-
hcfmusp.scopus.lastupdate2024-04-12-
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LIM/62 - Laboratório de Fisiopatologia Cirúrgica


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