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. 2021 May 25;21:150. doi: 10.1186/s12906-021-03318-x

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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 — Cell viability and proliferation were restrained when incubated with the aforementioned supernatant. a-d Change in the cell viability (% of the control group) when human bladder cancer cells T24 and EJ were cultured with the supernatant for 24 h or 48 h. (e-h) Effect of activated macrophages on T24 and EJ cell proliferation observed using EdU staining (200×). Red fluorescence denotes EdU staining, representing proliferating cells. Blue fluorescence denotes DAPI staining, representing the staining of nuclei. Statistical data analysis showed a downward trend in cell proliferation. ^*P < 0.05; ^**P < 0.01 compared with the control group(n = 3)