| Literature DB >> 35434532 |
Keith Long1, Zoe Vaughn1, Michael David McDaniels1, Sipak Joyasawal1, Aneta Przepiorski1, Emily Parasky1, Veronika Sander2, David Close1, Paul A Johnston1, Alan J Davidson2, Mark de Caestecker3, Neil A Hukriede1, Donna M Huryn1.
Abstract
Acute kidney injury (AKI), a sudden loss of kidney function, is a common and serious condition for which there are no approved specific therapies. While there are multiple approaches to treat the underlying causes of AKI, no targets have been clinically validated. Here, we assessed a series of potent, selective competitive inhibitors of histone deacetylase 8 (HDAC8), a promising therapeutic target in an AKI setting. Using biochemical assays, zebrafish AKI phenotypic assays, and human kidney organoid assays, we show that selective HDAC8 inhibitors can lead to efficacy in increasingly stringent models. One of these, PCI-34051, was efficacious in a rodent model of AKI, further supporting the potential for HDAC8 inhibitors and, in particular, this scaffold as a therapeutic approach to AKI.Entities:
Year: 2022 PMID: 35434532 PMCID: PMC9003639 DOI: 10.1021/acsptsci.1c00243
Source DB: PubMed Journal: ACS Pharmacol Transl Sci ISSN: 2575-9108