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Cited 37 time in webofscience Cited 38 time in scopus
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Epigenetics in osteoarthritis and its implication for future therapeutics

Authors
Im, Gun-IlChoi, You-Jeong
Issue Date
May-2013
Publisher
TAYLOR & FRANCIS LTD
Keywords
DNA methylation; epigenetics; genetics; histone deacetylase; histone modification; miRNA; osteoarthritis; therapeutics
Citation
EXPERT OPINION ON BIOLOGICAL THERAPY, v.13, no.5, pp 713 - 721
Pages
9
Indexed
SCIE
SCOPUS
Journal Title
EXPERT OPINION ON BIOLOGICAL THERAPY
Volume
13
Number
5
Start Page
713
End Page
721
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/18362
DOI
10.1517/14712598.2013.764410
ISSN
1471-2598
1744-7682
Abstract
Introduction: Changes occurring in the chondrocyte gene that control articular cartilage are important for the onset and progression of osteoarthritis (OA). However, actual development of the disease may be also controlled by changes in epigenome. Areas covered: Topics include the association of the three components of epigenetic modification, i.e., DNA methylation, histone modification, and microRNA expression, with the pathogenesis and progression of OA. The cross talk between genetics and epigenetics as well as the implication of epigenetics as a therapeutic measure for OA is also introduced. Expert opinion: Epigenetic markers that detect various chondrocyte phenotypes, including those involving chondrogenic differentiation, articular cartilage homeostasis, and progression of OA, may provide a novel means to detect early OA. Recent report of dietary supplement such as glucosamine that prevents demethylation of promoters of inflammatory cytokine is encouraging. Although already available, the toxicity and off-target side effects of histone deacetylase inhibitors are concerns for benign nonlethal disease like OA. miRNA-based treatment may present another therapeutic modality without potentially detrimental off-target side effects. Future studies are needed to search for additional miRNA that can modulate the course of OA and to identify key targets of currently known miRNA that impact OA pathogenesis and disease progression.
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