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Histone deacetylases and their inhibitors in inflammatory diseases.
Zhang, Sen-Yu; Zhang, Li-Ying; Wen, Ri; Yang, Ni; Zhang, Tie-Ning.
Affiliation
  • Zhang SY; Department of Pediatrics, PICU, Shengjing Hospital of China Medical University, Shenyang 110004, China.
  • Zhang LY; Department of Pediatrics, PICU, Shengjing Hospital of China Medical University, Shenyang 110004, China.
  • Wen R; Department of Pediatrics, PICU, Shengjing Hospital of China Medical University, Shenyang 110004, China.
  • Yang N; Department of Pediatrics, PICU, Shengjing Hospital of China Medical University, Shenyang 110004, China. Electronic address: yangni616@hotmail.com.
  • Zhang TN; Department of Pediatrics, PICU, Shengjing Hospital of China Medical University, Shenyang 110004, China. Electronic address: cmuztn@vip.qq.com.
Biomed Pharmacother ; 179: 117295, 2024 Aug 14.
Article in En | MEDLINE | ID: mdl-39146765
ABSTRACT
Despite considerable research efforts, inflammatory diseases remain a heavy burden on human health, causing significant economic losses annually. Histone deacetylases (HDACs) play a significant role in regulating inflammation (via histone and non-histone protein deacetylation) and chromatin structure and gene expression regulation. Herein, we present a detailed description of the different HDACs and their functions and analyze the role of HDACs in inflammatory diseases, including pro-inflammatory cytokine production reduction, immune cell function modulation, and anti-inflammatory cell activity enhancement. Although HDAC inhibitors have shown broad inflammatory disease treatment potentials, their clinical applicability remains limited because of their non-specific effects, adverse effects, and drug resistance. With further research and insight, these inhibitors are expected to become important tools for the treatment of a wide range of inflammatory diseases. This review aims to explore the mechanisms and application prospects of HDACs and their inhibitors in multiple inflammatory diseases.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Biomed Pharmacother Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Biomed Pharmacother Year: 2024 Document type: Article