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. 2019 Nov 22;19(1):630–638. doi: 10.3892/etm.2019.8238

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Copyright: © Yuan 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 3. — miR-138 inhibits the cell mobility and the regulated the expression of proteins related to apoptosis and invasion in vitro. (A) A transwell assay and (B) wound-healing assay were used to assess invasion. Magnification, ×200. (C) Caspase-3, Bax, Bcl-2 and MMP9 expression in the transfected cells was evaluated by western blot analysis, and β-actin was used as the control. Data are presented as the mean ± standard deviation. *P<0.05. miR, microRNA; MMP, matrix metalloproteinase; NC, negative control.