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. 2019 Sep 23;12:7809–7821. doi: 10.2147/OTT.S212596

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© 2019 Zhou et al.

This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).

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The effect of SB431542 on BC cells. A patient-derived BC cell line (patient no. 1) treated with the indicated concentrations of SB431542. The BC cells were harvested for MTT experiments (A) or qPCR experiments (B–D). The inhibition rates or effective rates of SB431542 on BC cell survival (A), E-cadherin (B), N-cadherin (C) and vimentin (D) are shown as the mean±SD. *P<0.05 versus a solvent control with SB431542.

Abbreviations: BC, bladder cancer; qPCR, quantitative real-time polymerase chain reaction.