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dc.contributor.authorKarakaş, Zeynep
dc.contributor.authorKuruca, Dürdane Serap
dc.contributor.authorAktaş, Zerrin
dc.contributor.authorÖncül, Mustafa Oral
dc.contributor.authorOğuz, Fatma
dc.contributor.authorSüleymanoğlu, Mediha
dc.contributor.authorErol, Ayşe
dc.contributor.authorAbatay Sel, Figen
dc.contributor.authorÖzdemir, İsa Aykut
dc.date.accessioned2022-02-18T09:15:56Z
dc.date.available2022-02-18T09:15:56Z
dc.identifier.citationSüleymanoğlu M., Erol A., Abatay Sel F., Özdemir İ. A. , Oğuz F., Kuruca D. S. , Aktaş Z., Karakaş Z., Öncül M. O. , "Anti-Leukemic Effect of Wharton Jelly Derived Mesenchymal Stem Cells in Vitro", VIII. International Congress of Molecular Medicine, 9 - 12 Kasım 2021, ss.1
dc.identifier.othervv_1032021
dc.identifier.otherav_2a0969a2-75ed-42fc-b3a2-85c3d95e7857
dc.identifier.urihttp://hdl.handle.net/20.500.12627/176857
dc.description.abstractBesides that mesenchymal stem cells (MSCs) have the capacity for self-renewal and multipotency, their possible anti-cancer effects making them a primary candidate for cell-based therapy. The purpose of this study was to evaluate in vitro anti leukemic effect of Wharton Jelly derived MSC (WJ-MSC) on the K562 and HL-60 cells.In this study, WJ-MSCs were isolated from an umbilical cord. According to standard culture conditions, the cells incubated and characterized by flow cytometry. For experiments, WJ-MSC and leukemic cells were incubated in the direct co-culture at a ratio of 1:5 (leukemia cells:WJ-MSC). We analyzed the apoptotic effect of WJ-MSCs on K562 and HL-60 cells with AnnexinV/PI assay by flow cytometry. After the direct co-culture of WJ-MSCs on leukemic cell lines, we observed anti-leukemic effect by inducing apoptosis. We had 2 groups of determination apoptosis with and without WJ-MSCs. In untreated and treated experimental groups for K562, we found increasing of apoptosis respectively (from 3,7% to 11,5%). For HL-60 cells, when compared between two groups apoptosis percentages were 15% (untreated) and 56% (treated). The increasing ratio of apoptotic cells was (approximately 3 folds) similar both for HL-60 and K562 cells.MSCs are known to inhibit tumor growth of hematopoitic and non-hematopoietic origin in vitro. Treatment with WJ-MSC led to potentproliferation inhibition of HL-60 and K562 cells with inducing apoptosis. Our results provide new insight into how WJ-MSCs inhibit tumor growth in vitro. In the future, WJ-MSCs may be an option for their clinical use for the inhibition of cancer cells.
dc.language.isoeng
dc.subjectKlinik Tıp (MED)
dc.subjectSağlık Bilimleri
dc.titleAnti-Leukemic Effect of Wharton Jelly Derived Mesenchymal Stem Cells in Vitro
dc.typeBildiri
dc.contributor.departmentİstanbul Üniversitesi , İstanbul Tıp Fakültesi , Temel Tıp Bilimleri Bölümü
dc.contributor.firstauthorID2774688


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