Molecular basis of organ fibrosis: potential therapeutic approaches - PubMed (original) (raw)
Review
. 2013 May;238(5):461-81.
doi: 10.1177/1535370213489441.
Affiliations
- PMID: 23856899
- DOI: 10.1177/1535370213489441
Free article
Review
Molecular basis of organ fibrosis: potential therapeutic approaches
Asish K Ghosh et al. Exp Biol Med (Maywood). 2013 May.
Free article
Abstract
Fibrosis, a non-physiological wound healing in multiple organs, is associated with end-stage pathological symptoms of a wide variety of vascular injury and inflammation related diseases. In response to chemical, immunological and physical insults, the body's defense system and matrix synthetic machinery respond to healing the wound and maintain tissue homeostasis. However, uncontrolled wound healing leads to scarring or fibrosis, a pathological condition characterized by excessive synthesis and accumulation of extracellular matrix proteins, loss of tissue homeostasis and organ failure. Understanding the actual cause of pathological wound healing and identification of igniter(s) of fibrogenesis would be helpful to design novel therapeutic approaches to control pathological wound healing and to prevent fibrosis related morbidity and mortality. In this article, we review the significance of a few key cytokines (TGF-β, IFN-γ, IL-10) transcriptional activators (Sp1, Egr-1, Smad3), repressors (Smad7, Fli-1, PPAR-γ, p53, Klotho) and epigenetic modulators (acetyltransferase, methyltransferases, deacetylases, microRNAs) involved in major matrix protein collagen synthesis under pathological stage of wound healing, and the potentiality of these regulators as therapeutic targets for fibrosis treatment. The significance of endothelial to mesenchymal transition (EndMT) and senescence, two newly emerged fields in fibrosis research, has also been discussed.
Keywords: ATp300; Egr1; EndMT; Fli-1; HDACi; PPAR-γ; Smad4; Smad7; Sp1; Wound healing; collagen; epigenetics; fibrosis; klotho; microRNA; p53; senescence.
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