Protein Acetylation in the Cardiorenal Axis The Promise of Histone Deacetylase Inhibitors

被引:109
作者
Bush, Erik W. [1 ]
McKinsey, Timothy A. [1 ]
机构
[1] Gilead Colorado Inc, Boulder, CO 80301 USA
关键词
acetylation; histone deacetylase; heart failure; kidney failure; fibrosis; MYOSIN HEAVY-CHAIN; SUBEROYLANILIDE HYDROXAMIC ACID; TO-MESENCHYMAL TRANSITION; REFRACTORY SOLID TUMORS; CHRONIC KIDNEY-DISEASE; VERSUS-HOST-DISEASE; PHASE-II TRIAL; CARDIAC-HYPERTROPHY; GENE-EXPRESSION; TRICHOSTATIN-A;
D O I
10.1161/CIRCRESAHA.109.209338
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Acetylation of histone and nonhistone proteins provides a key mechanism for controlling signaling and gene expression in heart and kidney. Pharmacological inhibition of protein deacetylation with histone deacetylase ( HDAC) inhibitors has shown promise in preclinical models of cardiovascular and renal disease. Efficacy of HDAC inhibitors appears to be governed by pleiotropic salutary actions on a variety of cell types and pathophysiological processes, including myocyte hypertrophy, fibrosis, inflammation and epithelial-to-mesenchymal transition, and occurs at compound concentrations below the threshold required to elicit toxic side effects. We review the roles of acetylation/deacetylation in the heart and kidney and provide rationale for extending HDAC inhibitors into clinical testing for indications involving these organs. (Circ Res. 2010; 106: 272-284.)
引用
收藏
页码:272 / 284
页数:13
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