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. 2023 Jan 23;14:1111912. doi: 10.3389/fphar.2023.1111912

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Copyright © 2023 Hu, Zhai, Tan, Chen, Zhang, Tan, Zheng, Gao, Wei, Wu and Yang.

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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HQ, FMNT and CS significantly increased the fluorescence intensity of E-cadherin (A, B), and decreased the fluorescence intensity of N-cadherin (C, D) and Vimentin (E, F) in HT29 and Caco2 cells. The fluorescence intensity of E-cadherin, N-cadherin, and Vimentin in HT29 and Caco2 cells were detected after treatment with HQ (100 mg/mL, 48 h), FMNT (100 μM, 48 h) or CS (100 μM, 48 h), respectively. The data represent the mean ± SD (n = 3). ^*** p < 0.001 compared with the control group.