Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/30375
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dc.contributor.authorKarakaş, Didem-
dc.contributor.authorUlukaya, Engin-
dc.date.accessioned2023-01-11T06:02:21Z-
dc.date.available2023-01-11T06:02:21Z-
dc.date.issued2017-
dc.identifier.citationKarakaş, D. vd. (2017). ''The MTT viability assay yields strikingly false-positive viabilities although the cells are killed by some plant extracts''. Turkish Journal of Biology, 41(6), 919-925.tr_TR
dc.identifier.issn1300-0152-
dc.identifier.urihttps://doi.org/10.3906/biy-1703-104-
dc.identifier.urihttps://journals.tubitak.gov.tr/biology/vol41/iss6/7/-
dc.identifier.uri1303-6092-
dc.identifier.urihttp://hdl.handle.net/11452/30375-
dc.description.abstractThe MTT assay is one of the often used cell viability/cytotoxicity assays. However, when the methanol extracts of plants are used to test their cytotoxic potential, interference may occur, resulting in false-positive viability results. Therefore, in this study, the reliability of the MTT assay was investigated in the case of plant use. The methanol extracts of three different plants (Hypericum adenotrichum, Salvia kronenburgii, and Pelargonium quercetorum) were tested in breast cancer cell lines (MCF-7 and MDA-MB-231) using the MTT assay and the results were compared to the ATP assay, which is a much more sensitive and reliable assay due to its interference-free feature. Additionally, decreased cell density was confirmed with phase-contrast microscopy and fluorescence staining (Hoechst 33342 dye). Although both of the viability/cytotoxicity assays are considered as metabolic assays, viabilities (in %) in the MTT assay were found to be strikingly higher when compared to the results with the ATP assay. Even in the case of total death, the MTT assay still produced artificial/false increases in viability. The morphology-based evaluation of viability/cytotoxicity by phase-contrast microscopy and Hoechst 33342 staining were greatly compatible with the ATP assay results. Overestimated (false) viabilities in the MTT assay suggests a serious interference between the MTT assay itself and the extracts used. Some ingredients of plants may have reducing activity (like the dehydrogenase activity of the cells) that converts the MTT compound into the colored formazan that is the principle of the assay. Therefore, the MTT assay may not be a suitable assay for some plant extracts, urging great caution when plants are useden_US
dc.language.isoenen_US
dc.publisherTÜBİTAKtr_TR
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectLife sciences & biomedicine - other topicsen_US
dc.subjectATP assayen_US
dc.subjectBreast canceren_US
dc.subjectCytotoxicityen_US
dc.subjectInterferenceen_US
dc.subjectMTT assayen_US
dc.subjectPlant extracten_US
dc.subjectRapid colorimetric assayen_US
dc.subjectTetrazolium salten_US
dc.subjectCyto-toxicityen_US
dc.subjectIn-vitroen_US
dc.subjectReductionen_US
dc.subjectGrowthen_US
dc.subjectAtpen_US
dc.subjectProliferationen_US
dc.subjectLinesen_US
dc.subjectSurvivalen_US
dc.titleThe MTT viability assay yields strikingly false-positive viabilities although the cells are killed by some plant extractsen_US
dc.typeArticleen_US
dc.identifier.wos000418253100007tr_TR
dc.identifier.scopus2-s2.0-85038415566tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Biyoloji Bölümü.tr_TR
dc.relation.bapBUAP(F)-2014/3en_US
dc.contributor.orcid0000-0002-6729-7908tr_TR
dc.identifier.startpage919tr_TR
dc.identifier.endpage925tr_TR
dc.identifier.volume41tr_TR
dc.identifier.issue6tr_TR
dc.relation.journalTurkish Journal of Biologyen_US
dc.contributor.buuauthorArı, Ferda-
dc.contributor.researcheridAAG-7012-2021tr_TR
dc.relation.collaborationYurt içitr_TR
dc.indexed.trdizinTrDizintr_TR
dc.identifier.pubmed30814856tr_TR
dc.subject.wosBiologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ4en_US
dc.contributor.scopusid24376085300tr_TR
dc.subject.scopusOvary Carcinoma; Drug Response; Irinotecanen_US
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