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dc.contributor.authorAydogmus-Ozturk, Fatma
dc.contributor.authorGunaydin, Keriman
dc.contributor.authorÖztürk, Mehmet
dc.contributor.authorJahan, Humera
dc.contributor.authorDuru, Mehmet E.
dc.contributor.authorChoudhary, Muhammad I.
dc.date.accessioned2020-11-20T14:49:42Z
dc.date.available2020-11-20T14:49:42Z
dc.date.issued2018
dc.identifier.issn0960-8931
dc.identifier.issn1473-5636
dc.identifier.urihttps://doi.org/10.1097/CMR.0000000000000487
dc.identifier.urihttps://hdl.handle.net/20.500.12809/1292
dc.descriptionOzturk, Mehmet/0000-0001-8932-4535; OZTURK, FATMA AYDOGMUS/0000-0001-6070-7452; DURU, Mehmet Emin/0000-0001-7252-4880en_US
dc.descriptionWOS: 000449641700003en_US
dc.descriptionPubMed ID: 30028780en_US
dc.description.abstractSideritis leptoclada O. Schwarz et P.H. Davis extracts were evaluated for its singlet oxygen production capacity using spectrophotometric method. The extracts producing singlet oxygen were then evaluated for cytotoxicity against malignant melanoma cancer (HT-144) and fibroblast (3T3) cell lines using the 3-[4,5-dimethylthiazole-2-yl]-2,5-diphenyl-tetrazolium bromide (MTT) assay. The photocytotoxicity against the HT-144 human melanoma cell line in the presence of illumination (similar to >= 400 nm) was also evaluated. In the standard MTT assay, the ethanol extract of S. leptoclada (100 mu g/ml) showed 83.49 +/- 3.33% inhibition of HT-144 cancer cells, whereas in the illuminated MTT assay, it showed 77.46 +/- 1.97% inhibition of HT-144 cancer cells. The effects of ethanol extract on reactive oxygen species production, apoptosis, and tumor necrosis factor-alpha secretion were also evaluated on HT-144 cell lines. The extract triggered an increase in intracellular reactive oxygen species production and tumor necrosis factor-alpha secretion compared with the respective controls. Thus, the ethanol extract may cause apoptosis. The LC-MS/MS analyses of S. leptoclada ethanolic extract showed that it has quinic acid (137213 +/- 11.25 mu g/g extract), malic acid (1468 +/- 0.16 mu g/g extract), chlorogenic acid (881.7 +/- 0.06 mu g/g extract), and apigetrin (223.2 +/- 0.13 mu g/g extract) as major constituents. The ethanolic extract of S. leptoclada should be further investigated as a potential treatment for malignant melanoma cancer. (C) 2018 Wolters Kluwer Health, Inc. All rights reserved.en_US
dc.description.sponsorshipResearch Fund of Istanbul UniversityIstanbul University [TP-19969]; ICCBS/PCMDen_US
dc.description.sponsorshipThis study is a part of the F.A.-O.'s PhD thesis and was supported by the Research Fund of Istanbul University project number: TP-19969). The authors would like to thank Dr Hasan Yildirim, Science Faculty, Department of Biology, Aegean University, Izmir, Turkey, for identification of the plant. F.A.-O. would also like to thank the staff of Dr Panjwani Center for Molecular Medicine and Drug Research (ICCBS), University of Karachi, Pakistan, for providing facilities for her studies.; This work was supported by the Research Fund of Istanbul University (project number: TP-19969) and ICCBS/PCMD.en_US
dc.item-language.isoengen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.item-rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectApoptosisen_US
dc.subjectCytotoxicityen_US
dc.subjectFibroblast (3T3) Cell Linesen_US
dc.subjectLC-MS/MSen_US
dc.subjectMalignant Melanoma (HT-144)en_US
dc.subjectPhotocytotoxicityen_US
dc.subjectReactive Oxygen Species Productionen_US
dc.subjectSideritis Leptoclada Oen_US
dc.subjectSchwarz Et P.H Davisen_US
dc.subjectTumor Necrosis Factor-Alpha Secretionen_US
dc.titleEffect of Sideritis leptoclada against HT-144 human malignant melanomaen_US
dc.item-typearticleen_US
dc.contributor.departmenten_US
dc.contributor.departmentTemp[Aydogmus-Ozturk, Fatma; Gunaydin, Keriman] Istanbul Univ, Fac Sci, Dept Mol Biol & Genet, Istanbul, Turkey -- [Aydogmus-Ozturk, Fatma] Mugla Sitki Kocman Univ, Fac Sci, Truffle Applicat & Res Ctr, Mugla, Turkey -- [Ozturk, Mehmet; Duru, Mehmet E.] Mugla Sitki Kocman Univ, Fac Sci, Dept Chem, Mugla, Turkey -- [Aydogmus-Ozturk, Fatma; Jahan, Humera; Choudhary, Muhammad I.] Univ Karachi, Panjwani Ctr Mol Med & Drug Res, Karachi, Pakistan -- [Choudhary, Muhammad I.] Univ Karachi, Int Ctr Chem & Biol Sci, HEJ Res Inst Chem, Karachi, Pakistan -- [Choudhary, Muhammad I.] King Abdulaziz Univ, Fac Sci, Dept Biochem, Jeddah, Saudi Arabiaen_US
dc.identifier.doi10.1097/CMR.0000000000000487
dc.identifier.volume28en_US
dc.identifier.issue6en_US
dc.identifier.startpage502en_US
dc.identifier.endpage509en_US
dc.relation.journalMelanoma Researchen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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