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. 2017 Sep 14;14(5):5994–6000. doi: 10.3892/ol.2017.6930

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Copyright: © Ke 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 2. — Effects of miR-10a on the proliferation, migration, and apoptosis of breast cancer cells. (A) The proliferation of MCF-7 and MDA-MB-231 cells transfected with miR-10a or anti-miR-10a was detected by MTT analysis. (B) Transwell analysis for the migration of MCF-7 and MDA-MB-231 cells. (C) The apoptosis of MCF-7 and MDA-MB-231 cells transfected with miR-10a was analyzed by flow cytometry. Each experiment was independently repeated three times. Values represent the mean ± standard deviation, *P<0.05 vs. miR-NC, ^#P<0.05 vs. anti-NC. miR, microRNA; NC, negative control.