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Review
. 2025 Jun;83(2):1375-1386.
doi: 10.1007/s12013-024-01587-0. Epub 2024 Oct 18.

Histone Deacetylases (HDACs) Roles in Inflammation-mediated Diseases; Current Knowledge

Affiliations
Review

Histone Deacetylases (HDACs) Roles in Inflammation-mediated Diseases; Current Knowledge

Saade Abdalkareem Jasim et al. Cell Biochem Biophys. 2025 Jun.

Abstract

The histone acetyl transferases (HATs) and histone deacetylases (HDACs), which are mostly recognized for their involvement in regulating chromatin remodeling via histone acetylation/deacetylation, have been shown to also change several non-histone proteins to regulate other cellular processes. Acetylation affects the activity or function of cytokine receptors, nuclear hormone receptors, intracellular signaling molecules, and transcription factors in connection to inflammation. Some small-molecule HDAC inhibitors are utilized as anticancer medications in clinical settings due to their capability to regulate cellular growth arrest, differentiation, and death. Here, we summarize our present knowledge of the innate and adaptive immunological pathways that classical HDAC enzymes control. The aim is to justify the targeted (or non-targeted) use of inhibitors against certain HDAC enzymes in inflammatory diseases such as arthritis, inflammatory bowel diseases (IBD), airways inflammation and neurological diseases.

Keywords: Arthritis; HDACs; IBD; Inflammation; Neuroinflammation.

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Conflict of interest statement

Compliance with ethical standards. Conflict of interest: The authors declare no competing interests.

References

    1. Zaib, S., Rana, N., & Khan, I. (2022). Histone Modifications and their Role in Epigenetics of Cancer. Current Medicinal Chemistry, 29(14), 2399–411. - PubMed - DOI
    1. Zhang, Y., Sun, Z., Jia, J., Du, T., Zhang, N., Tang, Y., Fang, Y., & Fang, D. (2021). Overview of Histone Modification. Advances in Experimental Medicine and Biology, 1283, 1–16. - PubMed - DOI
    1. Millán-Zambrano, G., Burton, A., Bannister, A. J., & Schneider, R. (2022). Histone post-translational modifications - cause and consequence of genome function. Nature Reviews Genetics, 23(9), 563–80. - PubMed - DOI
    1. Yoshizawa-Sugata, N., & Masai, H. (2023). Histone Modification Analysis of Low-Mappability Regions. Methods in Molecular Biology, 2519, 163–85. - PubMed - DOI
    1. Liu, R., Zhang, L., & Zhang, K. (2024). Histone modification in psoriasis: Molecular mechanisms and potential therapeutic targets. Clinical and Experimental Dermatology, 33(8), e15151.

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