Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/165960
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dc.contributor.authorGallego, Ana-
dc.contributor.authorMetón Teijeiro, Isidoro-
dc.contributor.authorBaanante, Isabel V.-
dc.contributor.authorOuazzani , Jamal-
dc.contributor.authorAdelin, Amelie-
dc.contributor.authorPalazón Barandela, Javier-
dc.contributor.authorBonfill Baldrich, Ma. Mercedes-
dc.contributor.authorMoyano Claramunt, Elisabet-
dc.date.accessioned2020-06-17T07:52:26Z-
dc.date.available2020-06-17T07:52:26Z-
dc.date.issued2017-03-01-
dc.identifier.issn0753-3322-
dc.identifier.urihttp://hdl.handle.net/2445/165960-
dc.description.abstractThe increasing rate of cancer incidence has encouraged the search for novel natural sources of anticancer compounds. The presence of small quantities of taxol and taxanes in Corylus avellana L. has impelled new potential applications for this plant in the field of biomedicine. In the present work, the cell viability-reducing activity of stems and leaves from three different hazel trees was studied against three human-derived cancer cell lines (HeLa, HepG2 and MCF-7). Both leaf and stem extracts significantly reduced viability of the three cell lines either after maceration with methanol or using taxane extraction methods. Since maceration reduced cell viability to a greater extent than taxane extraction methods, we scaled up the maceration extraction process using a method for solid/liquid extraction (Zippertex technology). Methanol leaf extracts promoted a higher reduction in viability of all cell lines assayed than stem extracts. Fractionation of methanol leaf extracts using silica gel chromatography led to the purification and identification of two compounds by HPLC-MS and NMR: (3R,5R)-3,5-dihydroxy-1,7-bis(4-hydroxyphenyl) heptane 3-O-β-d-glucopyranoside and quercetin-3-O-rhamnoside. The isolated compounds decreased viability of HeLa and HepG2 cells to a greater extent than MCF-7 cells. Our results suggest a potential use of C. avellana extracts in the pharmacotherapy of cervical cancer and hepatocarcinoma and, to a lesser extent, breast cancer.-
dc.format.extent8 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherElsevier Masson SAS-
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1016/j.biopha.2017.02.046-
dc.relation.ispartofBiomedicine & Pharmacotherapy, 2017, vol. 89, p. 565-572-
dc.relation.urihttps://doi.org/10.1016/j.biopha.2017.02.046-
dc.rights(c) Elsevier Masson SAS, 2017-
dc.subject.classificationFarmacologia-
dc.subject.classificationQuímica-
dc.subject.classificationCèl·lules canceroses-
dc.subject.classificationAvellaner-
dc.subject.classificationCàncer-
dc.subject.classificationCromatografia de líquids d'alta resolució-
dc.subject.otherPharmacology-
dc.subject.otherChemistry-
dc.subject.otherCancer cells-
dc.subject.otherHazel-
dc.subject.otherCancer-
dc.subject.otherHigh performance liquid chromatography-
dc.titleViability-reducing activity of Coryllus avellana L. extracts against human cancer cell lines-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec668770-
dc.date.updated2020-06-17T07:52:26Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Bioquímica i Fisiologia)
Articles publicats en revistes (Biologia, Sanitat i Medi Ambient)

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