Fig. 3

MiR-192 was the target of circ_0000282. a Bioinformatics was used to predict the binding site between circ_0000282 and miR-192. b-c Dual-luciferase reporter gene assay and RIP experiments proved that circ_0000282 adsorbed miR-192. d qRT-PCR was used to detect the effect of circ_0000282 overexpression or knockdown on miR-192 expression. e The correlation between circ_0000282 expression and miR-192 expression in OSA samples was analyzed. ns denotes no statistical significance, *** denotes P < 0.001