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. 2016 Mar 22;114(9):1012–1018. doi: 10.1038/bjc.2016.24

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Copyright © 2016 Cancer Research UK

From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/

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Knockdown of DLG1 expression by siRNA and shRNA significantly enhanced the migration and invasion ability of endometrial cancer cells. (A) Western blotting analysis of DLG1 and GAPDH expression in the stable DLG1 knockdown KLE clones. The silencing of DLG1 was observed in the clones 1 and 5. (B) Representative data of the wound healing assay. (C) The wound healing assay in Hec108, Hec1B, Hec59, and KLE cells. (D) Invasion assay using the Boyden chamber system in Hec108, Hec1B, Hec59, and KLE cells.