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Abstracts tagged "Histone Modification"

  • Abstract Number: 2731 • 2013 ACR/ARHP Annual Meeting

    An Acetyl-Histone Mimetic Blocks Proinflammatory Activation Of Rheumatoid Arthritis Fibroblast-Like Synoviocytes

    P. A. Kabala1, A.M. Grabiec1, C. Angiolilli1, Nicholas Smithers2, Jason Witherington3, Paul Peter Tak4, Rabinder Prinjha3 and Kris A. Reedquist5, 1Department of Experimental Immunology, Department of Clinical Immunology and Rheumatology Academic Medical Center, University of Amsterdam, Amsterdam, Netherlands, 2Immuno Inflammation, GlaxoSmithKline, Stevenage, United Kingdom, 3GlaxoSmithKline, Stevenage, United Kingdom, 4Academic Medical Center / University of Amsterdam, Department of Clinical Immunology and Rheumatology & GlaxoSmithKline, Amsterdam, Netherlands, 5Department of Experimental Immunology and Division of Clinical Immunology and Rheumatology, Academic Medical Center, University of Amsterdam, Amsterdam, Netherlands

    Background/Purpose: Genetic backgrounds and environmental factors do not completely explain the etiology of disease and predisposition to rheumatoid arthritis (RA), and increasing attention has turned…
  • Abstract Number: 2424 • 2013 ACR/ARHP Annual Meeting

    Investigation Of The Role Of Histone Deacetylases In Rheumatoid Arthritis Synovial Fibroblasts

    Sarah Hawtree1, Munitta Muthana1, Sarah Aynsley1, J. Mark Wilkinson2 and Anthony G. Wilson3, 1Infection and Immunity, University of Sheffield, Sheffield, United Kingdom, 2Academic Unit of Bone Metabolism, University of Sheffield, Sheffield, United Kingdom, 3Infection & Immunity, University of Sheffield, Sheffield, United Kingdom

    Background/Purpose: Rheumatoid arthritis (RA) is a chronic, autoimmune, inflammatory disease that affects synovial joints. A key characteristic of RA is hyperplasia of fibroblast-like synoviocytes (FLS).…
  • Abstract Number: 2399 • 2013 ACR/ARHP Annual Meeting

    Altered Histone Methylation Is Associated With IL-6 Dependent Matrix Metalloproteinases Gene Transcriptional Activation In Rheumatoid Arthritis Synovial Fibroblasts

    Yasuto Araki1,2, Takuma Tsuzuki Wada1,2, Kojiro Sato1, Kazuhiro Yokota1, Fumihiko Miyoshi1, Yu F. Asanuma3, Yuji Akiyama1 and Toshihide Mimura1,2, 1Department of Rheumatology and Applied Immunology, Faculty of Medicine, Saitama Medical University, Saitama, Japan, 2Project Research Division, Research Center for Genomic Medicine, Saitama Medical University, Saitama, Japan, 3Department of Rheumatology and Applied Immunology, Saitama Medical University, Saitama, Japan

    Background/Purpose: Rheumatoid arthritis (RA) is a chronic inflammatory autoimmune disease which causes progressive joint destruction. In spite of the modern medications including biologic reagents, it…
  • Abstract Number: 2216 • 2013 ACR/ARHP Annual Meeting

    Tubastatin A, a Selective Histone Deacetylase-6 Inhibitor, Suppresses Synovial Inflammation and Joint Destruction In a Collagen Antibody-Induced Arthritis Mouse Model

    Joong Kyong Ahn1, Jaejoon Lee2, Hyemin Jeong2, Jiwon Hwang2, Seulkee Lee2, Ji Young Chai3, Inyoung Kim2,4, Eun Chung Hong5, Eun-Kyung Bae5, Hoon-Suk Cha2 and Eun-Mi Koh2, 1Department of Medicine, Kangbuk Samsung hospital, Sungkyunkwan University School of Medicine, Seoul, South Korea, 2Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea, 3Division of Rheumatology, Jesang Hospital, Seongnam-si Gyeonggi-do, South Korea, 4MD, Seoul, South Korea, 5Samsung Biomedical Research Institute, Seoul, South Korea

    Background/Purpose: Histone deacetylases (HDAC) play a key role in regulating gene expression by deacetylasing histones, and HDAC inhibitors induce various cellular effects, including apoptosis, cell…
  • Abstract Number: 1625 • 2013 ACR/ARHP Annual Meeting

    Prolactin-Induced Interferon Regulatory Factor 1 Activation and Histone H4 Hyperacetylation In Monomac-6 Cells Correlating With Changes Seen In Monocytes From Systemic Lupus Erythematosus Patients

    Yiu Tak Leung1, Lihua Shi2, Kelly Maurer2, Li Song2, Michelle Petri3 and Kate Sullivan4, 1Medicine/Rheumatology, University of Pennsylvania, Philadelphia, PA, 2Immunology ARC 1216, The Children's Hospital of Philadelphia, Philadelphia, PA, 3Johns Hopkins University School of Medicine, Baltimore, MD, 4Allergy Immunology, The Children's Hospital of Philadelphia, Philadelphia, PA

    Background/Purpose: Epigenetic changes have been described in systemic lupus erythematosus (SLE) and offer a potential explanation for the chronicity of disease and missing heritability. Therapies…
  • Abstract Number: 1380 • 2013 ACR/ARHP Annual Meeting

    Histone Modifications In The Interluekin-6 Gene Promoter Region Of Rheumatoid Arthritis Synovial Fibroblasts

    Takuma Tsuzuki Wada1,2, Yasuto Araki1,2, Kazuhiro Yokota1, Fumihiko Miyoshi1, Kojiro Sato1 and Toshihide Mimura1,2, 1Department of Rheumatology and Applied Immunology, Faculty of Medicine, Saitama Medical University, Saitama, Japan, 2Project Research Division, Research Center for Genomic Medicine, Saitama Medical University, Saitama, Japan

    Background/Purpose: , Rheumatoid arthritis (RA) is a disease of unknown origin, which develops continuous inflammation and progressive joint destruction resulting from an autoimmune response mainly…
  • Abstract Number: L8 • 2013 ACR/ARHP Annual Meeting

    Overexpression of Set1 at the Promoter Contributes to cAMP Response Element Modulator Alpha Overexpression in Systemic Lupus Erythematosus

    Qing Zhang1, Huilin Zhang2, Hai Long1, Jieyue Liao3, Ming Zhao1, Xiangning Qiu1 and Qianjin Lu1, 1Department of Dermatology, Second Xiangya Hospital, Central South University, Changsha, China, 2Nursing Department, Second Xiangya Hospital, Central South University, Changsha, China, 3Department of Dermatology, Department of Dermatology, Second Xiangya Hospital, Central South University, Changsha, China

    Background/Purpose: In recent years, accumulating evidence has demonstrated that increased cAMP response element modulator α (CREMα) which contributes to IL-2 reduction and IL-17A overproduction in…
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All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

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