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. 2018 Jan 11;17(3):4392–4398. doi: 10.3892/mmr.2018.8423

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Copyright: © Wang 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. — FOXC1 silencing inhibits cervical cancer cell growth in vitro. (A) Western blotting was performed to confirm the effective knockdown of FOXC1. (B) Effect of FOXC1 on Hela and SiHa cell proliferation was measured by Cell Counting Kit-8 assay. (C) Apoptosis was detected by Annexin V-FITC and PI double staining and analyzed by flow cytometry when FOXC1 was silenced. *P<0.05, **P<0.01 vs. shRNA control. FOXC1, forkhead box protein C1; FITC, fluorescein isothiocyanate; PI, propidium iodide; shRNA, short hairpin RNA.