dc.contributor.author | Aydoğmuş-Öztürk, Fatma | |
dc.contributor.author | Jahan, Humera | |
dc.contributor.author | Beyazıt, Neslihan | |
dc.contributor.author | Günaydın, Keriman | |
dc.contributor.author | Choudhary, Muhammad Iqbal | |
dc.date.accessioned | 2020-11-20T14:42:17Z | |
dc.date.available | 2020-11-20T14:42:17Z | |
dc.date.issued | 2019 | |
dc.identifier.issn | 0301-4851 | |
dc.identifier.issn | 1573-4978 | |
dc.identifier.uri | https://doi.org/10.1007/s11033-019-04620-1 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12809/1050 | |
dc.description | 0000-0001-6070-7452 | en_US |
dc.description | WOS: 000463996700019 | en_US |
dc.description | PubMed ID: 30694454 | en_US |
dc.description.abstract | Melanoma is a cancer of melanocyte cells and has the highest global incidence. There is a need to develop new drugs for the treatment of this deadly cancer, which is resistant to currently used treatment modalities. We investigated the anticancer activity of visnagin, a natural furanochromone derivative, isolated from Ammi visnaga L., against malignant melanoma (HT 144)cell lines. The singlet oxygen production capacity of visnagin was determined by the RNO bleaching method while cytotoxic activity by theMTT assay. Further, HT 144 cells treated with visnagin were alsoexposed to visible light (400 nm) for 25min to examine the illuminationcytotoxicactivity.The apoptosis was measured by flow cytometry with annexin V/PI dual staining technique. The effect of TNF-secretion on apoptosis was also investigated. In standard MTT assay, visnagin (100 mu g/mL) exhibited 80.93% inhibitory activity against HT 144 cancer celllines, while in illuminated MTT assayat same concentration it showed lesser inhibitory activity (63.19%). Visnagin was induced apoptosis due to the intracellular generation of reactive oxygen species (ROS) andshowed an apoptotic effect against HT 144 cell lines by 25.88%. However, it has no effect on TNF- secretion. Our study indicates that visnagin can inhibit the proliferation of malignant melanoma, apparently by inducing the intracellular oxidative stress. | en_US |
dc.description.sponsorship | Research Fund of Istanbul UniversityIstanbul University [TP-19969] | en_US |
dc.description.sponsorship | This study is a part of F.A.o's Ph.D. thesis and was supported by the Research Fund of Istanbul University (Project Number: TP-19969). Prof. Dr. KerimanGunaydn would like to thank all staff of the Dr. Panjwani Center for Molecular Medicine and Drug Research (ICCBS), University of Karachi, Pakistan, for providing research facilities for her studies. | en_US |
dc.item-language.iso | eng | en_US |
dc.publisher | Springer | en_US |
dc.item-rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Visnagin | en_US |
dc.subject | Ammi Visnaga L | en_US |
dc.subject | Malignant Melanoma | en_US |
dc.subject | Apoptosis | en_US |
dc.title | The anticancer activity of visnagin, isolated from Ammi visnaga L., against the human malignant melanoma cell lines, HT 144 | en_US |
dc.item-type | article | en_US |
dc.contributor.department | MÜ, Köyceğiz Meslek Yüksekokulu, Bitkisel Ve Hayvansal Üretim Bölümü | en_US |
dc.contributor.institutionauthor | Aydoğmuş-Öztürk, Fatma | |
dc.identifier.doi | 10.1007/s11033-019-04620-1 | |
dc.identifier.volume | 46 | en_US |
dc.identifier.issue | 2 | en_US |
dc.identifier.startpage | 1709 | en_US |
dc.identifier.endpage | 1714 | en_US |
dc.relation.journal | Molecular Biology Reports | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |