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. 2020 Oct 27;20:520. doi: 10.1186/s12935-020-01607-y

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© The Author(s) 2020

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 — Plumbagin inhibited the migration of BCa cells by EMT suppression. a The expression levels of β-Catenin, Vimentin, MMP9, Slug and ZO-1 protein determined by western blotting assay when T24 and UMUC3 cells were treated with plumbagin at 0, 0.75, 1.5 μM. GAPDH was used as the internal control; b The anti-migration activity of plumbagin for UMUC3 cells was further evaluated by using wound healing assay; c Representative images of migrated BCa cells (T24 and UMUC3) after plumbagin treatment; d Quantitative analysis of wound healing assay for UMUC3 cells; Quantitative analysis of T24 e and UMUC3 (f) after plumbagin treatment for transwell assay. ***P < 0.001