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. 2017 Jun 14;14(2):1095–1103. doi: 10.3892/etm.2017.4608

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Copyright: © Liang 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 5. — miR-663b inhibitor-transfected CNE1 cells were further transfected with negative control (NC) siRNA or TUSC2 siRNA, respectively. (A) Quantitative PCR and (B) western blotting was used to examine the mRNA and protein expression of TUSC2. (C) MTT assay, (D) wound healing assay and (E) transwell assay were used to examine the cell proliferation, migration and invasion. **P<0.01 vs. miR-663b inhibitor + NC siRNA. TUSC2, tumor suppressor candidate 2; NC, negative control; siRNA, smal interfering RNA.