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. 2019 Apr 11;9:211. doi: 10.3389/fonc.2019.00211

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Copyright © 2019 Liu, Wang, Jiang, Zhang, Zhu, Lin, Jiang, Lin, Xiao, Fang and Guo.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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DDX5 interact with both HDGF and β-catenin in EC cells. Venn diagram depicting overlaps between HDGF and β-catenin proteins: the 22 common proteins are listed (A). Co-immunoprecipitation (Co-IP) detected the interaction of exogenous HDGF and DDX5 in RL95-2 cells (B). Co-IP detected the interaction of endogenous HDGF and DDX5 in RL95-2 cells (C). Nuclear co-localization of HDGF and DDX5, as well as β-catenin and DDX5 proteins, in EC cells by immunofluorescence under a scanning confocal microscope (D). DDX5 levels after HDGF knockdown, as assessed by western blotting (E). HDGF and β-catenin levels after DDX5 knockdown (F). Overexpression of β-catenin plasmid in shHDGF-EC cells increased DDX5 levels (G). DDX5 expression after β-catenin knockdown (H). DDX5 mRNA expression after HDGF knockdown, normalized to the expression of ARF5. One-way ANOVA and Dunnett's multiple comparison test ***P < 0.001 (I).