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SNHG3/miR‐577/SMURF1 axis could modulate the progression of prostate cancer cells. (A) The overexpression efficiency of SMURF1 was investigated via qRT‐PCR assay in PC3 cells and western blot assay. (B‐H) CCK‐8 assay, colony formation assay, tranwell assay, TUNEL assay, flow cytometry analysis, and western blot assay were implemented to detect the relationship between SNHG3 and SMURF1. **P < .01
