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dc.contributor.authorTunoglu, Servet
dc.contributor.authorYaylim, Ilhan
dc.contributor.authorFarooqi, Ammad Ahmad
dc.contributor.authorZeybek, Umit
dc.contributor.authorAKKOÇ, TUNÇ
dc.contributor.authorYenilmez, Ezgi Nurdan
dc.contributor.authorGenc, Deniz
dc.date.accessioned2021-03-05T12:28:30Z
dc.date.available2021-03-05T12:28:30Z
dc.date.issued2020
dc.identifier.citationYenilmez E. N. , Genc D., Farooqi A. A. , Tunoglu S., Zeybek U., AKKOÇ T., Yaylim I., "Mesenchymal Stem Cells Combined With IFN gamma Induce Apoptosis of Breast Cancer Cells Partially Through TRAIL", ANTICANCER RESEARCH, cilt.40, ss.5641-5647, 2020
dc.identifier.issn0250-7005
dc.identifier.otherav_ad582e89-c4ea-4241-ab65-3e872e79f90e
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/115663
dc.identifier.urihttps://doi.org/10.21873/anticanres.14577
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.language.isoeng
dc.subjectİç Hastalıkları
dc.subjectOnkoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectONKOLOJİ
dc.titleMesenchymal Stem Cells Combined With IFN gamma Induce Apoptosis of Breast Cancer Cells Partially Through TRAIL
dc.typeMakale
dc.relation.journalANTICANCER RESEARCH
dc.contributor.departmentİstanbul Teknik Üniversitesi , ,
dc.identifier.volume40
dc.identifier.issue10
dc.identifier.startpage5641
dc.identifier.endpage5647
dc.contributor.firstauthorID2358237


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