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10.18632/oncotarget.20334

http://scihub22266oqcxt.onion/10.18632/oncotarget.20334
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C5652762!5652762!29100368
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suck abstract from ncbi


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pmid29100368      Oncotarget 2017 ; 8 (44): 77041-9
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  • Glis family proteins are differentially implicated in the cellular reprogramming of human somatic cells #MMPMID29100368
  • Lee SY; Noh HB; Kim HT; Lee KI; Hwang DY
  • Oncotarget 2017[Sep]; 8 (44): 77041-9 PMID29100368show ga
  • The ground-breaking discovery of the reprogramming of somatic cells into pluripotent cells, termed induced pluripotent stem cells (iPSCs), was accomplished by delivering 4 transcription factors, Oct4, Sox2, Klf4, and c-Myc, into fibroblasts. Since then, several efforts have attempted to unveil other factors that are directly implicated in or might enhance reprogramming. Importantly, a number of transcription factors are reported to retain reprogramming activity. A previous study suggested Gli-similar 1 (Glis1) as a factor that enhances the reprogramming of fibroblasts during iPSC generation. However, the implication of other Glis members, including Glis2 and Glis3 (variants 1 and 2), in cellular reprogramming remains unknown.In this study, we investigated the potential involvement of human Glis family proteins, including hGlis1-3, in cellular reprogramming. Our results demonstrate that hGlis1, which is reported to reprogram human fibroblasts, promotes the reprogramming of human adipose-derived stromal cells (hADSCs), indicating that the reprogramming activity of Glis1 is not cell type-specific. Strikingly, hGlis3 promoted the reprogramming of hADSCs as efficiently as hGlis1. On the contrary, hGlis2 showed a strong negative effect on reprogramming.Together, our results reveal clear differences in the cellular reprogramming activity among Glis family members and provide valuable insight into the development of a new reprogramming strategy using Glis family proteins.
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