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. 2021 Mar 16;21:169. doi: 10.1186/s12935-021-01845-8

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© The Author(s) 2021

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 2 — Construction of colorectal cancer cell models with CDC42EP3 knockdown. a The fluorescence inside cells was observed and used to represent the transfection efficiency of shCDC42EP3 and shCtrl. b The efficiency of 3 shRNAs targeting CDC42EP3 was evaluated by qCPR. The knockdown efficiency of CDC42EP3 in RKO and HCT116 cells was evaluated by qPCR (c) and further verified by western blotting (d). The representative images were randomly selected from at least 3 independent experiments in duplicate. *P < 0.05, **P < 0.01, ***P < 0.001