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Review Article | Publishing Language: Chinese | Open Access

Research progress on histone acetylation/methylation in oral diseases

Yuchuan LUOFeifei LIFanyuan YUBei YINLing YE( )
State Key Laboratory of Oral Diseases & National Center for Stomatology & National Clinical Research Center for Oral Diseases & Department of Endodontics, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, China
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Abstract

Histone acetylation and methylation can affect chromatin conformation and regulate a variety of biological activities. Abnormal histone acetylation and methylation modifications are related to the occurrence and development of a variety of oral diseases. Histone acetylation and methylation increase or decrease in an orderly manner to regulate the development of teeth. Fluoride ions can destroy the balance between histone acetylation and methylation, which may be related to the occurrence of dental fluorosis. In addition, histone acetylation and methylation are involved in the regulation of oral inflammatory diseases. In the inflammatory microenvironment, the expression of histone acetyltransferase GCN5 decreases, and the expression of Dickkopf 1 (DKK1) decreases, activating the Wnt/β-catenin pathway and ultimately inhibiting the osteogenic differentiation of periodontal ligament stem cells. Enhancer of zeste homolog 2 (EZH2) and H3K27me3 levels were decreased in inflamed dental pulp tissues and cells. EZH2 inhibition inhibited the expression of interleukin (IL)-1b, IL-6 and IL-8 in human dental pulp cells under inflammatory stimulation. Histone acetylation/methylation modifications can interact with multiple signaling pathways to promote the occurrence and development of oral tumors and are related to the high invasiveness of salivary gland tumors. Small molecule drugs targeting histone acetylation and methylation-related enzymes can regulate the level of histone methylation/acetylation and have shown potential in the treatment of oral and maxillofacial diseases. For example, the histone deacetylase inhibitor vorinostat can inhibit the secretion of inflammation-related cytokines; it also promotes the maturation of odontoblasts and the formation of dentin-related matrix, demonstrating its potential in pulp preservation. Understanding the role of histone acetylation/methylation modifications in the occurrence and development of oral diseases will help promote research on epigenetic modifications in oral diseases and provide new perspectives for disease diagnosis and treatment.

CLC number: R78 Document code: A Article ID: 2096-1456(2024)06-0463-07

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Journal of Prevention and Treatment for Stomatological Diseases
Pages 463-469

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Cite this article:
LUO Y, LI F, YU F, et al. Research progress on histone acetylation/methylation in oral diseases. Journal of Prevention and Treatment for Stomatological Diseases, 2024, 32(6): 463-469. https://doi.org/10.12016/j.issn.2096-1456.2024.06.009

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Received: 06 November 2023
Revised: 07 January 2024
Published: 20 June 2024
© 2024 by Editorial Department of Journal of Prevention and Treatment for Stomatological Diseases