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. 2020 Jul 16;39:136. doi: 10.1186/s13046-020-01624-9

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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 — CASC9 promotes the proliferation but does not affect the apoptosis of BCCs. a and b The proliferation changes of BCCs were determined using CCK-8 assay in vitro. c and d The proliferation changes of BCCs were determined using Edu assay in vitro. e Tumours collected from mice are shown. f Tumor weight of shRNA-NC group was greater than that in the shRNA-CASC9 group. g Tumor growth of shRNA-NC was faster than that in the shRNA-CASC9 group. h The expression of Ki67 was determined using Immunohistochemistry. i and j The changes in bladder cancer cell apoptosis were determined using flow cytometry. The data are shown as the mean ± SD. *P < 0.05; **P < 0.01