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dc.contributor.authorTuncer, E.
dc.contributor.authorUnver-Saraydin, S.
dc.contributor.authorTepe, B.
dc.contributor.authorKaradayi, S.
dc.contributor.authorOzer, H.
dc.contributor.authorSen, M.
dc.contributor.authorKaradayi, K.
dc.contributor.authorInan, D.
dc.contributor.authorElagoz, S.
dc.contributor.authorPolat, Z.
dc.contributor.authorDuman, M.
dc.contributor.authorTuran, M.
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T10:03:07Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T10:03:07Z
dc.date.issued2013
dc.identifier.issn1107-0625
dc.identifier.issn2241-6293
dc.identifier.urihttps://hdl.handle.net/20.500.12418/8861
dc.descriptionWOS: 000322750600010en_US
dc.descriptionPubMed ID: 23613392en_US
dc.description.abstractPurpose: There has been a long-standing interest in the identification of medicinal plants and derived natural products for developing anticancer agents. This work aimed at investigating the antiprolipherative properties of Origanum acutidens (OA) on breast cancer. Methods: OA water extracts were studied for cytotoxicity against the breast cancer cell lines MCF-7, MDA-MB-468 and MDA-MB-231. In vitro apoptosis studies of these cancer cell lines were performed by annexin V staining in flow cytometry analyses. Immunohistochemistry studies for Ki-67 and caspase-7 of tumor tissue sections of dimethylbenzanthracene (DMBA) -induced mammary cancer in rats were also performed. TUNEL assay was used to detect apoptotic cells of tumor tissue. In vivo anticancer activity testing was carried out by inhibiting the growth of DMBA-induced mammary cancer in rats. Results: OA showed cytotoxicity on all 3 cancer cell lines. Annexin-positive cells level in OA-treated cell lines were significantly higher compared with untreated control cells (p=0.002). The expressions of caspase-7 protein and TUNEL-positive cells were much higher for the rats treated by OA, compared with the untreated control group (p<0.05). The expressions of the Ki-67 decreased in the treated groups compared with the control group (p<0.05). In vivo studies showed that the mean tumor volume inhibition ratio in OA-treated group was 41 % compared with the untreated rats (p<0.05). Conclusion: These results indicate that OA has antitumor activity against breast cancer cell lines.en_US
dc.description.sponsorshipScientific Research Project Fund of Cumhuriyet University [T-383]en_US
dc.description.sponsorshipThis work has been supported by the Scientific Research Project Fund of Cumhuriyet University under the project number T-383.en_US
dc.language.isoengen_US
dc.publisherIMPRIMATUR PUBLICATIONSen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectantitumor effecten_US
dc.subjectbreast canceren_US
dc.subjectoriganum acutidensen_US
dc.titleAntitumor effects of Origanum acutidens extracts on human breast canceren_US
dc.typearticleen_US
dc.relation.journalJOURNAL OF BUONen_US
dc.contributor.department[Tuncer, E. -- Ozer, H. -- Elagoz, S.] Cumhuriyet Univ, Fac Med, Dept Pathol, TR-58140 Sivas, Turkey -- [Unver-Saraydin, S. -- Inan, D.] Cumhuriyet Univ, Fac Med, Dept Histol & Embryol, TR-58140 Sivas, Turkey -- [Tepe, B.] Cumhuriyet Univ, Fac Med, Dept Mol Biol & Genet, TR-58140 Sivas, Turkey -- [Karadayi, S.] Baskent Univ, Fac Med, Dept Thorac Surg, Sivas, Turkey -- [Sen, M. -- Karadayi, K. -- Turan, M.] Cumhuriyet Univ, Fac Med, Dept Gen Surg, TR-58140 Sivas, Turkey -- [Polat, Z.] Cumhuriyet Univ, Fac Med, Dept Parasitol, TR-58140 Sivas, Turkey -- [Duman, M.] Kosuyolu Educ & Res Hosp, Istanbul, Turkeyen_US
dc.contributor.authorIDTEPE, Bektas -- 0000-0001-8982-5188;en_US
dc.identifier.volume18en_US
dc.identifier.issue1en_US
dc.identifier.endpage85en_US
dc.identifier.startpage77en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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