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. 2023 Dec 14;28:590. doi: 10.1186/s40001-023-01576-8

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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/. 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. 10 — Phosphorylation levels of ACBD3 protein in various tumors. A Summary of the correlation between various cancers and ACBD3 phosphorylation sites; B breast invasive carcinoma (BRCA); C head and neck squamous cell carcinoma (HNSC); D lung adenocarcinoma (LUAD); E kidney renal clear cell carcinoma (KIRC); F glioblastoma multiforme (GBM). The S316 locus expressed an upper phosphorylation level in BRCA when compared with normal tissues. The S20 locus exhibited a lower phosphorylation level in HNSC, and LUAD is the opposite. The S43 locus expressed an upper phosphorylation level in KIRC, LUAD, and GBM, and decreased in HNSC