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. 2019 Feb 14;41(4):2181–2193. doi: 10.3892/or.2019.7013

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Copyright: © Zhuo et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Figure 4. — Inhibitory effect of e6-PDT on the migration and invasion of bladder cancer cells. A wound healing assay was applied to measure the migration ability of (A and B) T24 and (C and D) 5637 cells following e6-PDT. Images were captured at the 0 and 24 h time points and the widths of each wound were measured. Scale bar=500 µm. (E) Cell invasion capacity of (F) T24 and (G) 5637 cells was evaluated using a Transwell assay. Scale bar=100 µm. Migrated cells were photographed and quantified following 48 h (n=3). **P<0.01 and ***P<0.001 vs. blank control group. e6-PDT, chlorophyllin e6-mediated photodynamic therapy.

Figure 4. — Inhibitory effect of e6-PDT on the migration and invasion of bladder cancer cells. A wound healing assay was applied to measure the migration ability of (A and B) T24 and (C and D) 5637 cells following e6-PDT. Images were captured at the 0 and 24 h time points and the widths of each wound were measured. Scale bar=500 µm. (E) Cell invasion capacity of (F) T24 and (G) 5637 cells was evaluated using a Transwell assay. Scale bar=100 µm. Migrated cells were photographed and quantified following 48 h (n=3). **P<0.01 and ***P<0.001 vs. blank control group. e6-PDT, chlorophyllin e6-mediated photodynamic therapy.