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10.3390/ijms161126075

http://scihub22266oqcxt.onion/10.3390/ijms161126075
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C4661932!4661932!26610487
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suck abstract from ncbi


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pmid26610487      Int+J+Mol+Sci 2015 ; 16 (11): 27945-55
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  • MiR542-3p Regulates the Epithelial-Mesenchymal Transition by Directly Targeting BMP7 in NRK52e #MMPMID26610487
  • Liu Z; Zhou Y; Yuan Y; Nie F; Peng R; Li Q; Lyu Z; Mao Z; Huang L; Zhou L; Li Y; Hao J; Ni D; Jin Q; Long Y; Ju P; Yu W; Liu J; Hu Y; Zhou Q
  • Int J Mol Sci 2015[Nov]; 16 (11): 27945-55 PMID26610487show ga
  • Accumulating evidence demonstrated that miRNAs are highly involved in kidney fibrosis and Epithelial-Eesenchymal Transition (EMT), however, the mechanisms of miRNAs in kidney fibrosis are poorly understood. In this work, we identified that miR542-3p could promote EMT through down-regulating bone morphogenetic protein 7 (BMP7) expression by targeting BMP7 3?UTR. Firstly, real-time PCR results showed that miR542-3p was significantly up-regulated in kidney fibrosis in vitro and in vivo. Moreover, Western blot results demonstrated that miR542-3p may promote EMT in the NRK52e cell line. In addition, we confirmed that BMP7, which played a crucial role in anti-kidney fibrosis and suppressed the progression of EMT, was a target of miR542-3p through Dual-Luciferase reporter assay, as did Western blot analysis. The effects of miR542-3p on regulating EMT could also be suppressed by transiently overexpressing BMP7 in NRK52e cells. Taken together, miR542-3p may be a critical mediator of the induction of EMT via directly targeting BMP7.
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