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10.1038/srep17618

http://scihub22266oqcxt.onion/10.1038/srep17618
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C4664936!4664936!26620926
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suck abstract from ncbi


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pmid26620926      Sci+Rep 2015 ; 5 (ä): ä
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  • MiR-181b regulates cisplatin chemosensitivity and metastasis by targeting TGF?R1/Smad signaling pathway in NSCLC #MMPMID26620926
  • Wang X; Chen X; Meng Q; Jing H; Lu H; Yang Y; Cai L; Zhao Y
  • Sci Rep 2015[]; 5 (ä): ä PMID26620926show ga
  • MicroRNAs (miRNAs) have been identified as important post-transcriptional regulators involved in various biological and pathological processes of cells, but their underlying mechanisms in chemosensitivity and metastasis have not been fully elucidated. The objective of this study was to identify miR-181b and its mechanism in the chemosensitivity and metastasis of NSCLC. We found that miR-181b expression levels were lower in A549/DDP cells compared with A549 cells. Functional assays showed that the overexpression of miR-181b inhibited proliferation, enhanced chemosensitivity to DDP, attenuated migration and metastatic ability in NSCLC cell lines in vitro and in vivo. TGF?R1 was subsequently identified as a novel functional target of miR-181b. TGF?R1 knockdown revealed similar effects as that of ectopic miR-181b expression, whereas overexpression of TGF?R1 rescued the function of miR-181b-mediated growth, chemosensitivity and metastasis in NSCLC cells. In addition, miR-181b could inactivate the TGF?R1/Smad signaling pathway. We also observed that decreased miR-181b expression and increased TGF?R1 expression were significantly associated with chemosensitivity to DDP and tumor metastasis in NSCLC patients. Consequently, miR-181b functions as a tumor suppressor and has an important role in proliferation, chemosensitivity to DDP and metastasis of NSCLC by targeting TGF?R1/Smad signaling pathway.
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