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. 2020 Feb 7;28(1):65–73. doi: 10.3727/096504019X15656904013079

Figure 2.

Figure 2

FOXD2-AS1 functions as a molecular sponge for miR-195. (A) Bioinformation analysis showed the potential interaction between FOXD2-AS1 and miR-195. (B) qRT-PCR was performed to assess the expression of miR-195 in TE-1/DDP cells that were transfected with a FOXD2-AS1-specific siRNA (si-FOXD2-AS1) or a negative control siRNA (si-NC). (C) qRT-PCR was performed to assess expression of miR-195 in TE-1/DDP cells that were transfected with a FOXD2-AS1 expression vector (FOXD2-AS1) or a control vector (vector). (D, E) A luciferase reporter assay revealed that miR-195 bound to the 3′-UTR of FOXD2-AS1. The results are shown as the means ± SEM. **p < 0.01 versus the control (vector) cells.