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. 2020 Jul 7;6(7):e04258. doi: 10.1016/j.heliyon.2020.e04258

Figure 3.

Figure 3

Downregulation of miR-362-3p promoted SKOV3 and HO8910 proliferation and migration. SKOV3 and HO8910 cells were transfected with miR-362-3p ASO, and miR-NC ASO was used as the negative control. After 24 h, the miR-362-3p levels of the transfected cells were assayed via qRT-PCR. The miR-362-3p level in the miR-NC ASO transfected cells was arbitrarily defined as 1 (A). Following miR-362-3p ASO transfection, the cell growth of SKOV3 and HO8910 were tested via MTT assay at indicated time point (0, 24, 48, 72h) (B). To assess cell migration, SKOV3 and HO8910 cells were added to the upper chamber with a noncoated membrane in each group. After 6 h, the cells in the lower chamber were counted (C). These experiments were performed in triplicate ∗P < 0.05.