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Updated: Feb 17, 2026

Assays for Validating Histone Acetyltransferase Inhibitors
Published on: August 6, 2020
Therapeutic effects of histone deacetylase inhibitors on kidney disease
1College of Pharmacy and Inje Institute of Pharmaceutical Sciences and Research, Inje University, 197 Inje-ro, Gimhae, Gyeongnam, 50834, Republic of Korea. pusoon@inje.ac.kr.
Abstract:
Increasing evidence has shown the involvement of histone deacetylases (HDACs) in the development and progression of various renal diseases, highlighting its inhibition as a promising therapeutic strategy to prevent kidney diseases. Accordingly, numerous studies have shown that HDAC inhibitors protect the kidneys from various diseases through their effects on multiple pathways, such as suppression of transforming growth factor-β signaling pathway and nuclear factor-κB signaling pathways, augmentation of apoptosis, and inhibition of angiogenesis. To develop more effective and less toxic isoform-selective HDAC inhibitors and further improve clinical outcomes, it is necessary to identify and understand the mechanisms involved in the pathogenesis and progression of renal diseases. This review focuses on the roles of HDAC inhibitors and the mechanisms involved in their therapeutic effects in experimental models of kidney diseases including glomerulosclerosis, tubulointerstitial fibrosis, glomerular and tubulointerstitial inflammation, lupus nephritis, polycystic kidney disease, and renal cell carcinoma (RCC).
Insights
Histone deacetylase (HDAC) inhibitors show promise for treating kidney diseases by targeting key pathways. Further research into HDAC inhibitor mechanisms is crucial for developing effective, less toxic therapies for renal conditions.
Area of Science:
- Nephrology
- Molecular Biology
- Pharmacology
Background:
- Histone deacetylases (HDACs) play a significant role in the development and progression of diverse renal diseases.
- HDAC inhibition is emerging as a potential therapeutic strategy for preventing kidney diseases.
Purpose of the Study:
- To review the roles of HDAC inhibitors in experimental kidney disease models.
- To elucidate the mechanisms underlying the therapeutic effects of HDAC inhibitors in renal pathologies.
- To guide the development of more effective and safer isoform-selective HDAC inhibitors.
Main Methods:
- Comprehensive literature review of studies investigating HDAC inhibitors in experimental renal disease models.
- Analysis of pathways targeted by HDAC inhibitors, including TGF-β and NF-κB signaling.
- Examination of effects on apoptosis and angiogenesis in the context of kidney disease.
Main Results:
- HDAC inhibitors demonstrate protective effects in various kidney diseases.
- Therapeutic mechanisms include suppression of pro-inflammatory and pro-fibrotic signaling pathways.
- HDAC inhibitors modulate apoptosis and angiogenesis, contributing to renoprotection.
Conclusions:
- HDAC inhibitors offer a promising therapeutic avenue for managing a spectrum of kidney diseases.
- Understanding HDAC inhibitor mechanisms is vital for optimizing their clinical application.
- Further development of isoform-selective HDAC inhibitors is warranted to improve patient outcomes in renal diseases.
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