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. 2022 Apr 26;13:760308. doi: 10.3389/fphar.2022.760308

TABLE 2.

Effect of HDAC inhibitors or gene deletion on renal fibrosis.

HDAC inhibitors or knockout mice Target Model Effects and mechanisms References
TSA Class I/II HDACs UUO Inhibit EMT; down regulate the TGF-β1 expression; inhibit the JNK/Notch-2 signaling pathways Ma et al. (2009), Tung et al. (2017)
MS-275 Class I HDACs UUO Suppress phosphorylation of Smad3, EGFR and STAT3; reduce the expression of TGF-β1 Liu et al. (2013)
RGFP966; HDAC3 knock-out mice HDAC3 UUO, AAN Depress the klotho expression Chen et al. (2021)
PCI34051 HDAC8 UUO Inhibit the development of EMT; preserve expression of BMP-7 and Klotho Zhang et al. (2020)
MC1568, HDAC4 siRNA HDAC4 UUO Reduce the expression of pro-fibrosis factors, TGF-β1/Smad3 and NF-κB; preserve expression of klotho, BMP-7 and Smad7 Xiong et al. (2019)
Tubastatin A, HDAC6 siRNA HDAC6 Ang II-induced hypertension Inhibit the transcription of TGF-β, Smad3, collagen I, and CTGF. Choi et al. (2015)
ACY-1215 HDAC6 UUO Inhibit the activation of TGF-β1/Smad3, EGFR/AKT, STAT3 and NF-κB signaling pathways Chen et al. (2020)
Quisinostat; HDAC11 siRNA HDAC11 UUO, Ang II-induced hypertension Suppress expression of Kruppel-like factor 15 Mao et al. (2020)

HDAC, histone deacetylase; TSA, Trichostatin A; UUO, unilateral ureteral obstruction; EMT, Epithelial–mesenchymal transition; TGF-β1, Transforming growth factor; JNK, c-Jun N-terminal kinase; EGFR, epidermal growth factor receptor; STAT3, Signal transducer and activator of transcription 3; BMP-7, Bone morphogenetic protein 7; NF-κB, Nuclear factor kappa B.