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. 2022 Sep 8;20:138. doi: 10.1186/s12964-022-00928-x

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© The Author(s) 2022

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. 4 — THZ1 shows antineoplastic properties in vivo. A Images of subcutaneous tumours from the vehicle or THZ1 treatment groups (n = 5). B, C. Tumour volume and weight of the subcutaneous tumour model. THZ1 treatment led to a significant reduction in tumour volume and weight. C Immunohistochemistry staining of Ki67 and cleaved caspase-3 in tissue sections from vehicle- or THZ1-treated subcutaneous tumours