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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. 4 — METTL3 enhances LINC00894 mRNA stability through the M6A-YTHDC2-dependent pathway. A. Enrichment of METTL3-mediated LINC00894 m6A modification using meRIP-qPCR. B-C. Detection of LINC00894 expression in actinomycin D-treated PTC cells overexpressing METTL3 using qRT‒PCR. D. Displaying the binding site of YTHDC2 and LINC00894 using the AnnoLnc2 database. E. Analysis of the correlation between YTHDC2 and LINC00894 using the starBase database. F. Detection of LINC00894 expression using qRT‒PCR following YTHDC2 overexpression. H-I. Detection of LINC00894 expression levels in actinomycin D-treated PTC cells overexpressing YTHDC2 using qRT‒PCR. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001