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. 2021 Sep 29;12(10):889. doi: 10.1038/s41419-021-04164-y

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© The Author(s) 2021

Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 7 — A The protein expression of OGT, O-GlcNAc, YAP, CDK19, and CDK8 was analyzed by WB in cells subjected to the indicated treatments. B, C Cell proliferation and colony-formation capacity were measured with CCK-8 cytotoxicity tests (B) and soft agar colony-formation assays (C), respectively, in Bel-7402 and Bel-7404 cells subjected to different treatments as indicated. D The possible mechanism of CA to inhibit diabetes-associated liver cancer. Data are shown as mean ± SD. **P < 0.01, ***P < 0.001, ****P < 0.0001.