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. 2018 Jan 29;17(4):5193–5201. doi: 10.3892/mmr.2018.8515

Figure 3.

Figure 3.

Cell invasion and luciferase reporter gene assays. (A) Representative images of the lower chamber of the Transwell invasion assay in different treatment groups. (B) Cell counts using a phase-contrast microscope revealed that Pter and miR-19a inhibitor groups exhibited significantly reduced cell invasion ability. This reduction was further enhanced in the Pter + miR-19a group. (C) Binding sequence between miR-19a and WT PTEN 3′-UTR, and the MT binding site of the PTEN 3′-UTR. PTEN was confirmed as a direct downstream target of miR-19a by TargetScanHuman. (D) A luciferase reporter gene activity assay was performed following co-transfection of PTEN 3′UTR MT/WT and miR-19a inhibitor or negative control. miR-19a inhibited the luciferase activity of the WT luciferase plasmid, while there was no significant difference when the miR-19a inhibitor was co-transfected with the MT luciferase plasmid. For part B, ***P<0.001 vs. blank or negative control groups; for part D, ***P<0.001, as indicated. In part B, the Pter-only treatment group was compared with the blank control group, while the miR-19a inhibitor and Pter + miR-19a inhibitor groups were compared with the negative control group. Pter, pterostilbene; miR, microRNA; WT, wild type; phosphatase and tensin homolog; UTR, untranslated region; MT/mut, mutant type; ns, not significant.