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Flower extracts of Filipendula ulmaria (L.) Maxim inhibit cell growth of human tumour cell lines

dc.contributor.authorLima, M. João
dc.contributor.authorSousa, Diana
dc.contributor.authorLima, Raquel T.
dc.contributor.authorCarvalho, Ana Maria
dc.contributor.authorFerreira, Isabel C.F.R.
dc.contributor.authorVasconcelos, M. Helena
dc.date.accessioned2015-11-04T10:10:34Z
dc.date.available2015-11-04T10:10:34Z
dc.date.issued2014
dc.description.abstractAccording to the World Health Organization, cancer is the leading cause of death worldwide and its mortality is expected to rise in the next few years. Despite all efforts, the current therapeutic arsenal is not sufficient to reduce these numbers. Therefore, it is imperative to identify new sources of anticancer drugs. Filipendula ulmaria (L.) Maxim is part of the ethnobothanical patrimony of the Iberian Peninsula. For centuries, it has been used as a medicinal species due to its rich antioxidant content, which includes flavonoids and ascorbic acid [l]. Nonetheless, little is known about its antiproliferative activity in cancer cells. Thus, the aims of this project were to: i) investigate if different flower extracts of F. ulmaria have cell growth inhibitory activity in human tumour cell lines and ii) study the mechanism of action of one of the most potent extracts. Four flower extracts obtained by different extraction methods (decoction, infusion, methanol and methanol:water 80:20, v!v) were screened for tumour cell growth inhibitory activity in three human tumour cell lines: NCI-H460 (non-small cell lung cancer), A375-C5 (melanoma) and MCF-7 (breast adenocarcinoma). One of the most potent extracts (obtained by decoction) was further studied in the NCI-H460 cell line (one of the most sensitive), by investigating its effect on viable cell number, programmed cell death, cellular proliferation and cell cycle profile. Results showed that all extracts have growth inhibitory activity in the studied cell lines, in particular the extract obtained by decoction (GI50 of 70.0 ± 8.6, 96.0 ± 12.4 and 63.3 ± 7.6 flg/mL in the NCI-H460, MCF-7 and A373-C5 cells, respectively). Further studies in the NCI-H460 cell line showed that this extract reduced viable cell number. Moreover, treatment with this extract resulted in a strong reduction of cellular proliferation, with a slight increase in the percentage of cells in the G l phase of the cell cycle. No significant alterations in programmed cell death were observed, although results showed a statistically significant increase in the cellular levels of p53 and p2l. Future work will confirm if this extract is non-toxic to human non-tumour cells.pt_PT
dc.identifier.citationLima, M. João; Sousa, Diana; Lima, Raquel T.; Carvalho, Ana Maria; Ferreira, Isabel C.F.R.; Vasconcelos, M. Helena (2014). Flower extracts of Filipendula ulmaria (L.) Maxim inhibit cell growth of human tumour cell lines. In XX Encontro Luso-Galego de Química. Porto. ISBN 978-989-98541-7-8pt_PT
dc.identifier.isbn978-989-98541-7-8
dc.identifier.urihttp://hdl.handle.net/10198/12262
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.relationNORTE-07-01 24-FEDER-000023pt_PT
dc.relationSMALL MOLECULES AS APOPTOSIS INDUCERS IN CANCER CELLS: INVESTIGATION OF THE MECHANISM OF ACTION
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.titleFlower extracts of Filipendula ulmaria (L.) Maxim inhibit cell growth of human tumour cell linespt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.awardTitleSMALL MOLECULES AS APOPTOSIS INDUCERS IN CANCER CELLS: INVESTIGATION OF THE MECHANISM OF ACTION
oaire.awardURIinfo:eu-repo/grantAgreement/FCT//SFRH%2FBPD%2F68787%2F2010/PT
oaire.citation.titleXX Encontro Luso-Galego de Químicapt_PT
person.familyNameCarvalho
person.familyNameFerreira
person.givenNameAna Maria
person.givenNameIsabel C.F.R.
person.identifierID G-7399-2011
person.identifier144781
person.identifier.ciencia-idD31A-35AF-E2A9
person.identifier.ciencia-id9418-CF95-9919
person.identifier.orcid0000-0001-5508-5935
person.identifier.orcid0000-0003-4910-4882
person.identifier.ridE-8500-2013
person.identifier.scopus-author-id20336503900
person.identifier.scopus-author-id36868826600
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT
relation.isAuthorOfPublication977f5254-f7c5-4c91-873f-2700ecd4692f
relation.isAuthorOfPublicationbd0d1537-2e03-41fb-b27a-140af9c35db8
relation.isAuthorOfPublication.latestForDiscovery977f5254-f7c5-4c91-873f-2700ecd4692f
relation.isProjectOfPublication506940d4-2643-4c8a-a077-9a30b043163a
relation.isProjectOfPublication.latestForDiscovery506940d4-2643-4c8a-a077-9a30b043163a

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