In vitro anti-leukemic effect of Wharton’s jelly derived mesenchymal stem cells

Background Mesenchymal stem cells (MSCs) have the ability to self-renew and are multi-potent. They are a primary candidate for cell-based therapy due to their potential anti-cancer effects. The aim of this study was to evaluate the in vitro anti-leukemic effect of Wharton’s Jelly-derived MSC (WJ-MSC...

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Veröffentlicht in:Molecular biology reports 2024-12, Vol.51 (1), p.595-595, Article 595
Hauptverfasser: Süleymanoğlu, Mediha, Erol Bozkurt, Ayşe, Abatay Sel, Figen, Özdemir, İsa Aykut, Savran Oğuz, Fatma, Kuruca, Dürdane Serap, Aktaş, Zerrin, Karakaş, Zeynep, Öncül, Mustafa Oral
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Sprache:eng
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Zusammenfassung:Background Mesenchymal stem cells (MSCs) have the ability to self-renew and are multi-potent. They are a primary candidate for cell-based therapy due to their potential anti-cancer effects. The aim of this study was to evaluate the in vitro anti-leukemic effect of Wharton’s Jelly-derived MSC (WJ-MSC) on the leukemic cell lines K562 and HL-60. Methods In this present study, WJ-MSCs were isolated from human umbilical cord. The cells were incubated according to the standard culture conditions 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). HUVEC cells were used as a non-cancerous cell line model. The apoptotic effect of WJ-MSCs on the cell lines was analyzed using Annexin V/PI apoptosis assay. Results After the direct co-culture of WJ-MSCs on leukemic cell lines, we observed anti-leukemic effects by inducing apoptosis. We had two groups of determination apoptosis with and without WJ-MSCs for all cell lines. Increased apoptosis rates were observed in K562 and HL-60 cell lines, whereas the apoptosis rates in HUVEC cells were low. Conclusions MSCs are known to inhibit the growth of tumors of both hematopoietic and non-hematopoietic origin in vitro. In our study, WJ-MSC treatment strongly inhibited the viability of HL-60 and K562 and induced apoptosis. Our results also provided new insights into the inhibition of tumor growth by WJ-MSCs in vitro. In the future, WJ-MSCs could be used to inhibit cancer cells in clinical applications.
ISSN:0301-4851
1573-4978
DOI:10.1007/s11033-024-09512-7