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. 2023 Jun 29;129(3):551–562. doi: 10.1038/s41416-023-02319-6

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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. 6 — a Hematoxylin–eosin (H&E) staining of the heart, liver, spleen, lung, kidney, and tumour in each group of mice. b Expression of alanine transaminase (ALT), aspartate transaminase (AST), blood urea nitrogen (BUN), and creatinine (Cr) in peripheral blood of mice serum. c Body-weight changes in mice receiving different treatment. d Representative in vivo images (IVIS) and quantification of luciferase in mice organs.