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. 2021 Jul 28;2021:4861749. doi: 10.1155/2021/4861749

Figure 3.

Figure 3

Overexpression of lncRNA OIP5-AS1 could promote the apoptosis and restrain EC cells' tumorigenic potential. (a) Measurement of apoptotic cells with OIP5-AS1 overexpression by FACS assay and calculated percentage of apoptotic cells. ∗∗∗P < 0.001 and P < 0.05. (b) Western blot analysis of cell death-related protein Bcl-2 and cleaved-caspase3, and the internal control is GAPDH. (c) Colony formation assay detected cell proliferation in OIP5-AS1-upregulated HEC-1-A cells and OIP5-AS1-downregulated KLE cells. (d, e) Transwell assay to test the invasion ability of HEC-1-A and KLE by altering the level of OIP5-AS1. ∗∗∗P < 0.001. (f) Wound healing assay to identify the migration capacity of two EC cells after transfecting the OIP5-AS1 vector and Si-OIP5-AS1 for 48 hours. P < 0.05.