Journal
EPIGENETICS
Volume 7, Issue 9, Pages 987-993Publisher
TAYLOR & FRANCIS INC
DOI: 10.4161/epi.21567
Keywords
fibrosis; myofibroblast; DNA methylation; 5-aza-2 '-deoxycytidine; histone modification; histone deacetylase inhibitors
Funding
- Science Foundation Ireland
- Health Research Board
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Fibrosis of any tissue is characterized by excessive extracellular matrix accumulation that ultimately destroys tissue architecture and eventually abolishes normal organ function. Although much research has focused on the mechanisms underlying disease pathogenesis, there are still no effective antifibrotic therapies that can reverse, stop or delay the formation of scar tissue in most fibrotic organs. As fibrosis can be described as an aberrant wound healing response, a recent hypothesis suggests that the cells involved in this process gain an altered heritable phenotype that promotes excessive fibrotic tissue accumulation. This article will review the most recent observations in a newly emerging field that links epigenetic modifications to the pathogenesis of fibrosis. Specifically, the roles of DNA methylation and histone modifications in fibrotic disease will be discussed.
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