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. 2023 Feb 7;14(2):90. doi: 10.1038/s41419-022-05547-5

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© The Author(s) 2023

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 — Mice were injected with HeLa cells with pcDNA3.1 or pcDNA3.1-PDHB-AS transfection or HeLa cells with or without HKF co-cultivation, and then in vivo assays were carried out. A Tumors in different groups were resected and displayed. B, C Tumor volumes and weights were measured under different conditions. D The levels of proliferation markers (Ki-67 and PCNA) as well as EMT markers (E-cadherin and N-cadherin) were detected in different groups of tissues. *P < 0.05, **P < 0.01.