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. 2018 Oct 29;17(1):221–229. doi: 10.3892/etm.2018.6895

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Copyright: © Chen et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Figure 6. — T98G and U251 cells which overexpressed miR-200a were transfected with a FOXA1 expression plasmid or blank vector. Following transfection, (A) western blotting was performed to examine the expression of FOXA1 protein. (B) An MTT, (C) EdU and (D) transwell assay were then performed to assess cell proliferation, viability and invasion, respectively. The magnification used for the EdU and transwell assays were ×40 and ×200, respectively. **P<0.01 vs. miR-200a+blank. miR, microRNA; FOXA1, forkhead box A1.