Figure 2. Interference with ANXA8 inhibited the proliferation and promoted the apoptosis of CAOV3 cells. (A) ANXA8 interference plasmid was constructed, and its interference efficacy was detected by RT-qPCR; (B) The transfection efficacy of ANXA8 interference plasmid was detected using western blotting; (C) CCK-8 assay was used to detect cell activity; (D) EdU staining was used to determine cell proliferation; (E) TUNEL staining was used to detect the level of apoptosis; (F) Western blot analysis of the expression of apoptosis-related proteins. *P<0.05, ***P<0.001 vs. shRNA-NC.