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Chemical composition and antiproliferative activity of Acalypha californica

dc.contributor.authorRascon-Valenzuela, L.
dc.contributor.authorJimenez-Estrada, M.
dc.contributor.authorVelazquez-Contreras, C.
dc.contributor.authorGaribay-Escobar, A.
dc.contributor.authorVilegas, Wagner [UNESP]
dc.contributor.authorCampaner, L. [UNESP]
dc.contributor.authorCoqueiro, A. [UNESP]
dc.contributor.authorRobles-Zepeda, R. E.
dc.contributor.institutionUniv Sonora
dc.contributor.institutionUniv Nacl Autonoma Mexico
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2015-10-22T06:12:29Z
dc.date.available2015-10-22T06:12:29Z
dc.date.issued2015-07-01
dc.description.abstractAcalypha californica Benth., is a plant in the northwestern region from Mexico, commonly known as "cancer herb" and used in traditional medicine for treating cancer. In the present study we have investigated the antiproliferative activity of methanolic extract of A. californica and its fractions in cancer cell lines and phytochemical analysis and mechanism of apoptosis of the fractions with antiproliferative activity. The antiproliferative activity of methanol extract and its fractions of solvents were evaluated by MTT assay against the M12.A(k).C3.F6, RAW 264.7, HeLa and L929 cell lines. Active fractions were fractionated by molecular exclusion chromatography, HPLC and MPLC. The identification of compounds was performed by NMR and FIA-ESI-IT-MS/MS analysis. Apoptotic mechanism was analyzed by flow cytometry, determining the reduction in the mitochondrial membrane potential (JC-1) and the activity of caspases 3,8 and 9. Cell viability assays showed that the hexane fraction of the methanol extract of the plant has significant effects against cancer lines RAW 264.7 (IC50 = 52.08 +/- 1.06 mu g/mL) and HeLa (IC50 = 46.77 +/- 1.09 mu g/mL), the residual fraction showed a selective effect on cell lines M12.A(k).C3.F6 (IC50 = 59.90 +/- 1.05 mu g/mL), RAW 264.7 (IC50 = 58.93 +/- 1.26 mu g/mL) and HeLa (IC50 = 50.11 +/- 1.135 mu g/mL) compared to the control cell line L929 (IC50 = 100.00 +/- 1.09 mu g/mL). The chemical characterization of the active fractions allowed the identification of p-sitosterol and stigmasterol in hexane fraction and some phenolic acids, proanthocyanidins and flavonoids in the residual fraction. The methanol extract and hexane fraction reduces mitochondrial membrane potential significantly and activates caspases 3, 8 and 9. Because of the antiproliferative activity observed, our results provide a rational basis for the use of extracts of A. californica in treating various types of cancer in traditional medicine from Mexico. The extracts induce apoptosis via activation of caspases. (C) 2015 Elsevier B.V. All rights reserved.en
dc.description.affiliationUniv Sonora, Div Ciencias Biol &Salud, Dept Ciencias Quim Biol, Encinas Rosales Hermosil, Sonora, Mexico
dc.description.affiliationUniv Nacl Autonoma Mexico, Inst Quim, Dept Prod Nat, Mexico City 04510, DF, Mexico
dc.description.affiliationUNESP Sao Paulo State Univ, Sao Paulo, Brazil
dc.description.affiliationUnespUNESP Sao Paulo State Univ, Sao Paulo, Brazil
dc.description.sponsorshipConsejo Nacional de Ciencia y Tecnologia (CONACYT)
dc.description.sponsorshipIdConsejo Nacional de Ciencia y Tecnologia (CONACYT): 83462
dc.format.extent48-54
dc.identifier.citationIndustrial Crops And Products, v. 69, p. 48-54, 2015.
dc.identifier.doi10.1016/j.indcrop.2015.02.004
dc.identifier.issn0926-6690
dc.identifier.lattes7927877224326837
dc.identifier.orcid0000-0003-3032-2556
dc.identifier.urihttp://hdl.handle.net/11449/129595
dc.identifier.wosWOS:000355365300007
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofIndustrial Crops And Products
dc.relation.ispartofjcr3.849
dc.relation.ispartofsjr1,091
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectAntiproliferative activityen
dc.subjectChemical compositionen
dc.subjectApoptotic mechanismen
dc.titleChemical composition and antiproliferative activity of Acalypha californicaen
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.lattes7927877224326837
unesp.author.orcid0000-0002-5279-4020[8]
unesp.author.orcid0000-0003-3032-2556[5]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, São Vicentept
unesp.departmentCiências Biológicas - IBCLPpt

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