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. 2018 Sep 11;9(9):916. doi: 10.1038/s41419-018-0976-0

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 6 — a, b HepG2 and MHCC-97H cells were treated as described in Fig. 5. Western blot (a) and real-time PCR analysis (b) were carried out to assess the protein and mRNA expression of E-cadherin, respectively. c The activity of the CDH1 promoter was determined by Luciferase Reporter assays. d ChIP analysis was conducted in HepG2 cells to determine the binding of FOXJ2 to CDH1 promoter. IgG was a negative control. ***P < 0.001