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. 2020 Apr 3;20:108. doi: 10.1186/s12935-020-1157-7

Fig. 3.

Fig. 3

ZFPM2-AS1 acted as sponge of miR-3612. a Both cytoplasmic and nuclear expression of ZFPM2-AS1 was measured via qRT-PCR after subcellular fractionation. b FISH probed the expression of ZFPM2-AS1 in cytoplasm and nucleus. c DIANA and starBase revealed the predicted miRNAs that might bind with ZFPM2-AS1. d RNA pull-down assay detected the enrichment of the indicated miRNAs in ZFPM2-AS1 probe group. e The binding site between miR-3612 and ZFPM2-AS1 was exhibited (upper). Luciferase activity of ZFPM2-AS1-WT or ZFPM2-AS1-MUT was monitored by luciferase reporter assay following NC mimics or miR-3612 mimics transfection (lower). f RIP assay examined the enrichment of ZFPM2-AS1 and miR-3612 in Anti-Ago2 group. g Overexpression efficiency of ZFPM2-AS1 in SHP-77 and DMS-53 cells was detected by qRT-PCR. h qRT-PCR evaluated the regulatory effects of ZFPM2-AS1 on miR-3612 expression in SHP-77 and DMS-53 cells. *P < 0.05, **P < 0.01, *** P < 0.001