| Literature DB >> 24321371 |
Hui Tao1, Kai-Hu Shi2, Jing-Jing Yang3, Cheng Huang4, Hong-Ying Zhan1, Jun Li5.
Abstract
Cardiac fibrosis is an important pathological feature of cardiac remodeling in heart diseases. The molecular mechanisms of cardiac fibrosis are unknown. Histone deacetylases (HDACs) are enzymes that balance the acetylation activities of histone acetyltransferases on chromatin remodeling and play essential roles in regulating gene transcription. In recent years, the role of HDACs in cardiac fibrosis initiation and progression, as well as the therapeutic effects of HDAC inhibitors, has been well studied. Moreover, numerous studies indicated that HDAC activity is associated with the development and progression of cardiac fibrosis. In this review, the innovative aspects of HDACs are discussed, with respect to biogenesis, their role in cardiac fibrosis. Furthermore, the potential applications of HDAC inhibitors in the treatment of cardiac fibrosis associated with fibroblast activation and proliferation.Entities:
Keywords: Cardiac fibrosis; ECM; Epigenetic; Extracellular matrix; FGF; Fibroblast; Fibroblast growth factor; HATs; HDACs; Histone acetyltransferases; Histone deacetylase; Histone deacetylases; Histone deacetylation; IGF-II/mannose 6-phosphate receptor; IGF-IIR/Man-6-P; MEF2; Myocyte enhancer factor-2; NRVMs; Neonatal rat ventricular myocytes; PDGF; PKD1; Platelet-derived growth factor; Proliferation; Protein kinase D1; TGF-β1; TIMPs; Tissue inhibitors of matrix metalloproteinases; Transforming growth factor β1; α-SMA; α-smooth muscle actin
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Year: 2013 PMID: 24321371 DOI: 10.1016/j.cellsig.2013.11.037
Source DB: PubMed Journal: Cell Signal ISSN: 0898-6568 Impact factor: 4.315