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10.1038/s41598-018-27583-y

http://scihub22266oqcxt.onion/10.1038/s41598-018-27583-y
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C6031697!6031697!29973668
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suck abstract from ncbi


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pmid29973668      Sci+Rep 2018 ; 8 (ä): ä
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  • MiR-99b-5p and miR-203a-3p Function as Tumor Suppressors by Targeting IGF-1R in Gastric Cancer #MMPMID29973668
  • Wang Z; Zhao Z; Yang Y; Luo M; Zhang M; Wang X; Liu L; Hou N; Guo Q; Song T; Guo B; Huang C
  • Sci Rep 2018[]; 8 (ä): ä PMID29973668show ga
  • MicroRNAs (miRNAs) have been explored in many critical cellular processes, including proliferation and apoptosis. The purpose of this study was to detect the biological function and regulation of miR-99b-5p and miR-203a-3p in gastric cancer (GC). Here, we demonstrated that miR-99b-5p/203a-3p were downregulated in both GC tissues and cell lines. MiR-99b-5p/203a-3p overexpression reduced GC cell proliferation and cell cycle progression in vitro. Notably, we combined bioinformatics tools with biological validation assays to demonstrate that insulin-like growth factor 1 receptor (IGF-1R) is a direct co-target and functional mediator of miR-99b-5p/203a-3p in GC cells. Mechanistically, the AKT pathway, which is downstream of IGF-1R, is essential for the functional roles of miR-99b-5p/203a-3p in GC cells. Taken together, our data revealed that IGF-1R is a direct co-target of miR-99b-5p/203a-3p, and miR-99b-5p/203a-3p may function as tumor suppressive miRNAs by negatively regulating IGF-1R expression in GC cells.
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