Publication:
Mesenchymal Stem Cells Combined With IFN gamma Induce Apoptosis of Breast Cancer Cells Partially Through TRAIL

dc.contributor.authorAKKOÇ, TUNÇ
dc.contributor.authorsYenilmez, Ezgi Nurdan; Genc, Deniz; Farooqi, Ammad Ahmad; Tunoglu, Servet; Zeybek, Umit; Akkoc, Tunc; Yaylim, Ilhan
dc.date.accessioned2022-03-12T22:44:23Z
dc.date.accessioned2026-01-10T19:24:06Z
dc.date.available2022-03-12T22:44:23Z
dc.date.issued2020
dc.description.abstractBackground: Mesenchymal stem cells (MSCs) have gained remarkable attention because of their ability to dualistically regulate tumor growth. The main objective of this study was to evaluate the apoptotic effects of human bone marrow-derived (hBM) MSCs in combination with interferon gamma (IFN-gamma) on MCF-7 breast cancer cells, and to determine the cytokines involved in the apoptotic process. Materials and Methods: hBM-MSCs were co-cultured with MCF-7 cells either directly and indirectly for 72 h in-vitro. Levels of tumor necrosis factor-related apoptosis-inducing ligand (TRAIL), apoptosis and cytokines were analyzed. Results: hBM-MSCs increased the apoptosis of MCF-7 cells partially through TRAIL in vitro. IFN-gamma enhanced the apoptotic effect of hBM-MSCs (p<0.001). Conclusion: hBM-MSCs in combination with IFN-gamma might be a suitable therapy for breast cancer.
dc.identifier.doi10.21873/anticanres.14577
dc.identifier.eissn1791-7530
dc.identifier.issn0250-7005
dc.identifier.pubmed32988888
dc.identifier.urihttps://hdl.handle.net/11424/236424
dc.identifier.wosWOS:000582679500038
dc.language.isoeng
dc.publisherINT INST ANTICANCER RESEARCH
dc.relation.ispartofANTICANCER RESEARCH
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectMCF-7
dc.subjectbreast cancer
dc.subjectmesenchymal stem cells
dc.subjectTRAIL
dc.subjectINTERFERON-ALPHA
dc.subjectMETASTASIS
dc.subjectGROWTH
dc.subjectPROMOTE
dc.titleMesenchymal Stem Cells Combined With IFN gamma Induce Apoptosis of Breast Cancer Cells Partially Through TRAIL
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage5647
oaire.citation.issue10
oaire.citation.startPage5641
oaire.citation.titleANTICANCER RESEARCH
oaire.citation.volume40

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