A novel disease-modifying osteoarthritis drug candidate targeting Runx1. Issue 5 (5th October 2012)

• Record Type: Journal Article
• Authors: Yano, Fumiko; Hojo, Hironori; Ohba, Shinsuke; Fukai, Atsushi; Hosaka, Yoko; Ikeda, Toshiyuki; Saito, Taku; Hirata, Makoto; Chikuda, Hirotaka; Takato, Tsuyoshi; Kawaguchi, Hiroshi; Chung, Ung-il
• Is Part Of: Annals of the rheumatic diseases. Volume 72:Issue 5(2013)
• Page Start: 748
• Page End: 753
• Publication Date: 2012-10-05
• Subjects: Chondrocytes -- Knee Osteoarthritis -- Osteoarthritis; Rheumatism -- Periodicals; 616.723005
• DOI: 10.1136/annrheumdis-2012-201745
• Languages: English
• ISSNs: 0003-4967

Abstract

Abstract : Objectives: To identify a new disease-modifying osteoarthritis drug (DMOAD) candidate that can effectively repair cartilage by promoting chondrogenic differentiation and halt osteoarthritis (OA) progression by suppressing aberrant hypertrophy. Methods: We screened 2500 natural and synthetic small compounds for chondrogenic agents via four steps using the Col2GFP-ATDC5 system and identified a small thienoindazole derivative compound, TD-198946, as a novel DMOAD candidate. We tested its efficacy as a DMOAD via intra-articular injections directly into the joint space in a surgically-induced mouse model of OA both at the onset (prevention model) and 4 weeks after (repair model) OA induction. The downstream molecules were screened by microarray analysis. We further investigated the mechanism of the drug action and its molecular target using in vitro and in vivo assays. Results: TD-198946 strongly induced chondrogenic differentiation without promoting hypertrophy in cell and metatarsal organ cultures. When administered directly into the joint space, TD-198946 successfully prevented and repaired degeneration of the articular cartilage. TD-198946 exerted its effect through the regulation of Runx1 expression, which was downregulated in both mouse and human OA cartilage compared with normal tissue. Conclusions: Our data suggest that TD-198946 is a novel class of DMOAD candidate, and that targeting Runx1 will provide a promising new approach in the development of disease-modifying drugs against OA.