Abstract
Background/Purpose:
Several inflammatory cytokines and intracellular signaling pathways have been targeted in drug development with varying clinical results. Improved understanding of the intracellular signaling’s modulation of the extracellular matrix turnover could aid in selecting novel anti-inflammatory treatments for inflammatory arthritis. The aim of this study was to investigate the effect of small molecule inhibitors targeting 4 main pro-inflammatory signaling pathways (p38, Syk, IκBα, and STAT) on Oncostatin M (OSM) and Tumor Necrosis Factor α (TNFα) stimulated cartilage.
Several inflammatory cytokines and intracellular signaling pathways have been targeted in drug development with varying clinical results. Improved understanding of the intracellular signaling’s modulation of the extracellular matrix turnover could aid in selecting novel anti-inflammatory treatments for inflammatory arthritis. The aim of this study was to investigate the effect of small molecule inhibitors targeting 4 main pro-inflammatory signaling pathways (p38, Syk, IκBα, and STAT) on Oncostatin M (OSM) and Tumor Necrosis Factor α (TNFα) stimulated cartilage.
Original language | English |
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Article number | 969 |
Journal | Arthritis and Rheumatology |
Volume | 69 |
Issue number | Suppl. 10 |
ISSN | 2326-5205 |
Publication status | Published - 2017 |
Event | 2017 ACR/ARHP Annual Meeting - San Diego, United States Duration: 3 Nov 2017 → 8 Nov 2017 http://acrabstracts.org/meetings/2017-acrarhp-annual-meeting/ |
Conference
Conference | 2017 ACR/ARHP Annual Meeting |
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Country/Territory | United States |
City | San Diego |
Period | 03/11/2017 → 08/11/2017 |
Internet address |