Anti-cancer efficiency of natural killer cells differentiated from human adipose tissue-derived mesenchymal stem cells and transfected with miRNA150
dc.contributor.author | Karlitepe A. | |
dc.contributor.author | Kabadayi H. | |
dc.contributor.author | Vatansever S. | |
dc.contributor.author | Gurdal M. | |
dc.contributor.author | Gunduz C. | |
dc.contributor.author | Ercan G. | |
dc.date.accessioned | 2019-10-26T21:16:14Z | |
dc.date.available | 2019-10-26T21:16:14Z | |
dc.date.issued | 2017 | |
dc.department | Ege Üniversitesi | en_US |
dc.description.abstract | Aim: The aim of this study is to investigate the effects of miR150 transfection on NK-like cells differentiated from adipose tissue derived mesenchymal stem cells (AD-MSCs). Methods: NK-like cells were differentiated from AD-MSCs and activated by miR150 transfection. Transfected/non-Transfected NK-like cells were characterized by immunohistochemical and RTPCR analyzes. Apoptotic efficiency of the transfected/non-Transfected NK-like cells on pancreatic cancer cells PANC1 were determined by TUNEL and RT-PCR. Results: In miR150-Transfected cells, the increased expression of NK cell-specific genes such as GKMB, KIR2DL2, CD16, CD56, NKG2D, NKp46 and increased immunoreactivity of NK cell-specific surface marker CD314 (NKG2D) were evident. TUNEL assays showed that NK-like cells with/without transfection induced apoptosis in PANC1 cells in the same manner. The decrease in oncogene expression and the increase in the tumor suppressor gene expression in PANC1 cells upon co-culture with NK-like cells differentiated from AD-MSCs were more prominent following miRNA150 transfection. Conclusion: It was shown in vitro that NK-like cells could be obtained by differentiation from AD-MSCs and their efficiency could be increased via miR150 transfection. The results are encouraging for further clinical studies in improvement of immunotherapeutic approaches for cancer therapy. Copyright © Experimental Oncology, 2017. | en_US |
dc.description.sponsorship | This study was supported by grant No. 214S650 from the Turkish Scientific and Technological Research Institute (TUBITAK). -- | en_US |
dc.identifier.endpage | 218 | en_US |
dc.identifier.issn | 1812-9269 | |
dc.identifier.issue | 3 | en_US |
dc.identifier.pmid | 28967637 | en_US |
dc.identifier.scopusquality | Q4 | en_US |
dc.identifier.startpage | 212 | en_US |
dc.identifier.uri | https://hdl.handle.net/11454/16170 | |
dc.identifier.volume | 39 | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Morion LLC | en_US |
dc.relation.ispartof | Experimental Oncology | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Adipose tissue derived mesenchymal stem cells | en_US |
dc.subject | Mirna150 | en_US |
dc.subject | Natural killer cells | en_US |
dc.subject | Pancreatic cancer | en_US |
dc.title | Anti-cancer efficiency of natural killer cells differentiated from human adipose tissue-derived mesenchymal stem cells and transfected with miRNA150 | en_US |
dc.type | Article | en_US |