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. 2024 Jul 16;16:91. doi: 10.1186/s13148-024-01709-8

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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. 1 — Dox treatment led to H3K27ac accumulation in cardiomyocytes. A, B Representative western blot (A) and statistical data (B) showing the levels of H3K27ac from the cardiomyocytes treated with Dox for 24 h, n = 6 per group. C, D Representative immunostaining image (C) and mean fluorescence intensity (D) for H3K27ac (green) in the cardiomyocytes treated with Dox for 24 h; CTNT denotes cardiac troponin T (red); Nuclei were stained with DAPI (blue)