ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstracts tagged "WNT Signaling"

  • Abstract Number: 2929 • 2017 ACR/ARHP Annual Meeting

    WNT5A Promotes Tissue Fibrosis By Wnt/PCP-Dependent Activation of Latent TGF-β

    Chih-Wei Chen1, Thuong Trinh-Minh2, Neng-Yu Lin2, Yun Zhang3, Florian Groeber4, Christian Beyer5, Georg Schett6 and Jörg Distler7, 1Department of Internal Medicine 3 – Rheumatology and Immunology, Friedrich-Alexander-University Erlangen-Nürnberg (FAU) and University Hospital Erlangen, Erlangen, Germany, Erlangen, Germany, 2Department of Internal Medicine 3 – Rheumatology and Immunology, Friedrich-Alexander-University Erlangen-Nürnberg (FAU) and University Hospital Erlangen, Erlangen, Germany, 3Department of Internal Medicine 3 and Institute for Clinical Immunology, Department of Internal Medicine 3 and Institute for Clinical Immunology, Friedrich-Alexander-University of Erlangen-Nuremberg and University Hospital Erlangen, Erlangen, Germany, 4Translational Center Würzburg, Fraunhofer Ins. IGB, Würzburg, Germany, 5Department of Internal Medicine 3 and Institute for Clinical Immunology, Friedrich-Alexander-University of Erlangen-Nuremberg and University Hospital Erlangen, Erlangen, Germany, 6Friedrich-Alexander-University Erlangen-Nürnberg (FAU), Department of Internal Medicine 3 – Rheumatology and Immunology, Universitätsklinikum Erlangen, Erlangen, Germany., Erlangen, Germany, 7Department of Internal Medicine 3 – Rheumatology and Immunology, Universitätsklinikum Erlangen, Friedrich-Alexander-University Erlangen-Nürnberg (FAU), Erlangen, Germany

    Background/Purpose:  Canonical Wnt/β-catenin signaling has emerged as a core pathway of fibrosis. They role of non-canonical Wnt signaling, however, has not been systematically studied. In…
  • Abstract Number: 2120 • 2016 ACR/ARHP Annual Meeting

    Discovery of a Small Molecule Inhibitor of the Wnt Pathway (SM04690) As a Potential Treatment for Degenerative Disc Disease

    Charlene Barroga1, Vishal Deshmukh1, Luis Dellamary1, Josh Stewart1, Haide Hu2, John Hood2 and Yusuf Yazici1, 1Samumed, LLC, San Diego, CA, 2Samumed, LLC (formerly), San Diego, CA

    Background/Purpose: Degenerative Disc Disease (DDD), one of the main causes of low back pain, is characterized by degeneration of intervertebral disc, nucleus pulposus (NP), and…
  • Abstract Number: 2143 • 2016 ACR/ARHP Annual Meeting

    A Small Molecule, SM04690, Has Inhibitory Effects on the Wnt Pathway and Inflammation in Vitro, with Potential Implications for the Treatment of Osteoarthritis

    Vishal Deshmukh1, Maureen Ibanez1, Charlene Barroga1, John Hood2 and Yusuf Yazici1, 1Samumed, LLC, San Diego, CA, 2Samumed, LLC (formerly), San Diego, CA

    Background/Purpose:   Osteoarthritis (OA) involves thinning cartilage and increased subchondral bone. Amongst many cellular processes, inflammation has been associated with OA. Wnt signaling plays a…
  • Abstract Number: 2350 • 2016 ACR/ARHP Annual Meeting

    Radiographic Outcomes from a Randomized, Double-Blind, Placebo-Controlled, Phase 1 Study of a Novel, Intra-Articular, Injectable, Wnt Inhibitor (SM04690) in the Treatment of Osteoarthritis of the Knee

    Christopher J. Swearingen1, Sharmila Majumdar2, Ismail Simsek1, Anita DiFrancesco1, Jeymi Tambiah1 and Yusuf Yazici1, 1Samumed, LLC, San Diego, CA, 2University of California San Francisco, San Francisco, CA

    Background/Purpose: Knee osteoarthritis (OA) is characterized by pain, functional impairment, disability, and joint space narrowing due to degradation of articular cartilage and bone remodeling. The…
  • Abstract Number: 2704 • 2016 ACR/ARHP Annual Meeting

    Discovery of a Small Molecule Inhibitor of the Wnt Pathway (SM04755) As a Potential Topical Treatment for Psoriasis

    Vishal Deshmukh1, Melinda Pedraza1, Maureen Ibanez1, Luis Dellamary1, Josh Stewart1, Timothy Seo1, Benoit Melchior1, John Hood2 and Yusuf Yazici1, 1Samumed, LLC, San Diego, CA, 2Samumed, LLC (formerly), San Diego, CA

    Background/Purpose: Psoriasis is an auto-immune disease of the skin, characterized by inflammation and fibrosis producing patches of red, itchy and scaly skin. Wnt signaling plays…
  • Abstract Number: 2719 • 2016 ACR/ARHP Annual Meeting

    Discriminating Value of Calprotectin in Disease Activity and Progression of Non-Radiographic Axial Spondyloarthritis and Ankylosing Spondylitis

    Jinxian Huang1, Zhihua Yin2, Guoxiang Song3, Shengjin Cui4, Jinzhao Jiang4 and Lijun Zhang4, 1Rheumatology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China, 2Rheumatology, The Fourth People’s Hospital of Shenzhen, Shenzhen, China, 3The Third People’s Hospital of Shenzhen, Shenzhen, China, 4The University of Hong Kong-Shenzhen Hospital, Shenzhen, China

    Background/Purpose:  Due to the limitation of early diagnosis of ankylosing spondylitis (AS), updated criteria in recent years introduced the concept of axial spondyloarthritis (axSpA) and…
  • Abstract Number: 2993 • 2016 ACR/ARHP Annual Meeting

    Membrane-Type 1 Matrix Metalloproteinase Controls Osteo- and Chondrogenesis By a Proteolysis-Independent Mechanism Mediated By Its Cytoplasmic Tail

    Yang Qing1, Mukundan Attur2, Thorsten Kirsch3, You Jin Lee3, Shoshana Yakar4, Zhomgbo Liu5, Steven B. Abramson6 and Paolo Mignatti7, 1Medicine, New York University School of Medicine, New York, NY, 2Rheumatology Research, NYU - Hospital for Joint Diseases, New York, NY, 3Orthopaedic Surgery, New York University, New York, NY, 4Basic Science and Craniofacial Biology, College of Dentistry, New York University, New York, NY, 5New York University, New York, NY, 6Dept of Rheumatology/Medicine, Hosp for Joint Diseases/NYU, New York, NY, 7Medicine, New York University, New York, NY

    Background/Purpose:  We aimed to understand the mechanism by which membrane-type 1 matrix metalloproteinase (MT1-MMP, MMP-14) controls bone and cartilage homeostasis. MT1-MMP, a cell-membrane-bound proteinase with…
  • Abstract Number: 2994 • 2016 ACR/ARHP Annual Meeting

    Binding of Periostin to Discoidin Domain Receptor-1 (DDR1) Promotes Cartilage Degeneration By Inducing MMP-13 Expression

    Yang Qing1, Paolo Mignatti2, Austin Ramme3, Thorsten Kirsch3, Jyoti Patel4 and Mukundan Attur4, 1Medicine, New York University School of Medicine, New York, NY, 2Medicine, New York University, New York, NY, 3Orthopaedic Surgery, New York University, New York, NY, 4Rheumatology Research, NYU - Hospital for Joint Diseases, New York, NY

    Background/Purpose:  We and others have previously shown that periostin (Postn) expression is dramatically elevated in cartilage and sub-chondral bone in OA patients and surgical models…
  • Abstract Number: 2995 • 2016 ACR/ARHP Annual Meeting

    WISP1/CCN4 Aggravates Experimental Osteoarthritis and Is Associated with Disease Progression in Early Osteoarthritis Patients

    Martijn H. van den Bosch1, Arjen B. Blom1, Azusa Maeda2, Tina Kilts2, Wim B. van den Berg3, Peter L. van Lent3, Marian F. Young2 and Peter M. van der Kraan1, 1Experimental Rheumatology, Radboud university medical center, Nijmegen, Netherlands, 2NIDCR/NIH, Bethesda, MD, 3Radboud university medical center, Nijmegen, Netherlands

    Background/Purpose:  Many osteoarthritis (OA) patients show synovial activation, which is thought to be involved in joint destruction. Previously, we described strongly increased expression of Wnt2b…
  • Abstract Number: 809 • 2016 ACR/ARHP Annual Meeting

    Micrornas Targeting the Wnt Signalling Pathway in Black African Patients with Diffuse Cutaneous Systemic Sclerosis

    Mohammed Tikly1, Jacqueline Frost2, Michèle Ramsay3, Eulalia Marti Puig4, Raquel Rabionet4, Xavier Estivill4 and Marc Friedländer5, 1Division of Rheumatology, Chris Hani Baragwanath Academic Hospital, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa, 2University of the Witwatersrand, Johannesburg, South Africa, 3Division of Human Genetics, Sydney Brenner Institute for Molecular Biosciences, University of the Witwatersrand, Johannesburg, South Africa, 4Center for Genomic Regulation, Barcelona, Spain, 5Department of Molecular Biosciences, The Wenner-Gren Institute, Science for Life Laboratory, Stockholm, Sweden

    Background/Purpose: Systemic sclerosis (SSc) is a complex autoimmune disease involving the immune system, vasculature and extracellular matrix [1]. Dysregulation of the Wnt pathway has been implicated in…
  • Abstract Number: 1096 • 2016 ACR/ARHP Annual Meeting

    Augmentation of Wnt Signaling By IL-1β in Fibroblast-like Synoviocytes

    Satoshi Yamasaki1, Yusuke Yoshida2 and Eiji Sugiyama2, 1Hiroshima University Hospital, Hiroshima, Japan, 2Department of Clinical Immunology and Rheumatology, Hiroshima University Hospital, Hiroshima, Japan

    Background/Purpose: Wnt family proteins canonically stabilize β-catenin to activate T-cell factor (TCF) for the transcription of several genes, including Runx2, which is important for osteoblastogenesis.…
  • Abstract Number: 1104 • 2016 ACR/ARHP Annual Meeting

    Discovery of a Small Molecule Inhibitor of the Wnt Pathway (SM04755) As a Potential Topical Treatment for Chronic Tendinopathy

    Vishal Deshmukh1, Timothy Seo1, Maureen Ibanez1, Luis Dellamary1, Josh Stewart1, John Hood2 and Yusuf Yazici1, 1Samumed, LLC, San Diego, CA, 2Samumed, LLC (formerly), San Diego, CA

    Background/Purpose: Chronic tendinopathy is an inflammatory and degenerative condition caused by injuries or overuse. Current therapeutic options focus on alleviating the symptoms and pain rather…
  • Abstract Number: 1444 • 2016 ACR/ARHP Annual Meeting

    Differential Expression of Wnt Inhibitors before and after Joint Inflammation Onset in Rat Arthritis Could Partly Explain Paradoxical Effect of Sclerostin Inhibition

    Guillaume Courbon1, Raphaelle Lamarque2, Marie-Thérèse Linossier2, Norbert Laroche2, Thierry Thomas3, Laurence Vico2 and Hubert Marotte3, 1SAINBIOSE INSERM U1059, University of Lyon, Saint-Etienne, France, 2SAINBIOSE INSERM U1059, University of Lyon, Saint Etienne, France, 3SAINBIOSE INSERM U1059 and Rheumatology department, University of Lyon and University Hospital of Saint Etienne, Saint Etienne, France

    Background/Purpose:  Periarticular bone loss in rheumatoid arthritis is considered to be mainly related to synovial inflammation, leading to uncoupling between decreased bone formation and increased…
  • Abstract Number: 1848 • 2016 ACR/ARHP Annual Meeting

    Adenosine A2A Receptor (A2AR) Stimulates Collagen Type III Synthesis Via β-Catenin Activation in Vitro and in Vivo

    Jin Zhang1, Gibran Shaikh2, Carmen Corciulo3, Tuere Wilder3, Miguel Perez-Aso1, Aranzazu Mediero1 and Bruce Cronstein1, 1Medicine, Division of Rheumatology, NYU School of Medicine, New York, NY, 2Department of Medicine, NYU School of Medicine, New York, NY, 3Department of Medicine, Division of Rheumatology, NYU School of Medicine, New York, NY

    Background/Purpose: Fibrosis of skin and other organs is a hallmark of Scleroderma.  We and others have previously reported that A2AR plays a role in skin…
  • Abstract Number: 1856 • 2016 ACR/ARHP Annual Meeting

    Discovery of a Small Molecule Inhibitor of the Wnt Pathway (SM04755) As a Potential Topical Treatment for Scleroderma

    Vishal Deshmukh1, Allison Hood2, Maureen Ibanez1, Luis Dellamary1, Josh Stewart1, Timothy Seo1, John Hood2 and Yusuf Yazici1, 1Samumed, LLC, San Diego, CA, 2Samumed, LLC (formerly), San Diego, CA

    Background/Purpose: Scleroderma is an autoimmune fibrotic disease, which presents skin manifestations among others. The Wnt pathway plays an important role in inflammation, skin fibrosis, and…
  • « Previous Page
  • 1
  • 2
  • 3
  • 4
  • Next Page »
Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

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.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology