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Epigenetics in Rheumatoid Arthritis: A Primer for Rheumatologists

  • RHEUMATOID ARTHRITIS (LW MORELAND, SECTION EDITOR)
  • Published:
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Abstract

Epigenetic anomalies are emerging as key pathogenic features of rheumatoid arthritis (RA). The effect of epigenetics in RA ranges from contributing to complex disease mechanisms to identifying biomarkers for early diagnosis and response to therapy. This review focuses on three key epigenetic areas in RA, namely DNA methylation, histone modification, and expression and/or function of microRNAs. Epigenomics studies of DNA methylation have identified alterations of genome-wide DNA methylation in cells from patients with rheumatoid arthritis. Histone modification studies have focused on histone acetylation, which tends to be increased in RA. Preclinical studies show that inhibitors of histone deacetylases are effective in cellular and animal models of RA. Genome-wide and candidate microRNA surveys identified increased or reduced expression of selected microRNAs in rheumatoid arthritis. These microRNA are either pro or anti-inflammatory in multiple cell types or affect osteoclast physiology and the pathogenesis of bone erosion. Defining epigenetic contributions to the pathogenesis of RA, especially in combination with understanding genetic associations, could lead to novel therapy and a clearer understanding of disease risk.

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Acknowledgments

Funding was provided, in part, by the Rheumatology Research Foundation Disease Targeted Innovative Research Award. This is manuscript #1647 from the La Jolla Institute for Allergy and Immunology.

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Gary S. Firestein has held stock/stock options in Ignyta Inc. Nunzio Bottini declares that he has no conflict of interest.

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This article does not contain any studies with human or animal subjects performed by any of the authors.

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Correspondence to Nunzio Bottini or Gary S. Firestein.

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This article is part of the Topical Collection on Rheumatoid Arthritis

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Bottini, N., Firestein, G.S. Epigenetics in Rheumatoid Arthritis: A Primer for Rheumatologists. Curr Rheumatol Rep 15, 372 (2013). https://doi.org/10.1007/s11926-013-0372-9

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