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. 2023 Dec 20;14:235. doi: 10.1007/s12672-023-00843-8

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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 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/.

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Fig. 4 — Molecular mechanisms by which m⁶A modifications regulate the biological functions of BCa. Writer proteins METTL3 and METTL14 are involved in BCa proliferation, invasion, migration, angiogenesis, cell adhesion and immune escape. Eraser protein FTO is involved in BCa proliferation, invasion, and migration. Reader proteins YTHDF1 and IGF2BP3 are involved in BCa proliferation