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. 2024 Jan 30;24:47. doi: 10.1186/s12935-024-03240-5

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© The Author(s) 2024

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 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. 6 — LINC00894 inhibits PTC malignant phenotypes through the Hippo signalling pathway. A-B. TCGA analysis was performed to identify differentially expressed genes in normal thyroid tissue and PTC tissue. C. KEGG pathway enrichment analysis. D. Analysis of the correlation between LINC00894 and TAZ, YAP, LATS1, and MST1 using the starBase database. E. Analysis of the correlation between METTL3 and TAZ, YAP, LATS1, and MST1 using the starBase database. F. Protein expression levels of Hippo signalling pathway-related proteins after pcDNA-LINC00894 transfection in KTC-1 cells according to Western blotting. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001