Possible Repositioning of an Oral Anti-Osteoporotic Drug, Ipriflavone, for Treatment of Inflammatory Arthritis via Inhibitory Activity of KIAA1199, a Novel Potent Hyaluronidase

• Published in: International journal of molecular sciences Vol. 23; no. 8; p. 4089
• Main Authors: Koike, Hiroshi, Nishida, Yoshihiro, Shinomura, Tamayuki, Ohkawara, Bisei, Ohno, Kinji, Zhuo, Lisheng, Kimata, Koji, Ushida, Takahiro, Imagama, Shiro
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 07.04.2022; MDPI
• Subjects: Accumulation; Animals; Arthritis; Arthritis, Experimental - drug therapy; Arthritis, Experimental - metabolism; Biomedical materials; Cartilage; Cell adhesion & migration; CEMIP; Chondrosarcoma; Collagen; collagen-induced arthritis; Drug dosages; Drug Repositioning; Enzyme-linked immunosorbent assay; Enzymes; Extracellular matrix; FDA approval; Fibroblasts; Fibroblasts - metabolism; hyaluronan; Hyaluronic Acid - pharmacology; hyaluronidase; Hyaluronoglucosaminidase - metabolism; Inflammation; inflammatory arthritis; Ipriflavone; Isoflavones; KIAA1199; Matrix Metalloproteinase 1 - genetics; Matrix Metalloproteinase 1 - metabolism; Metabolism; Mice; Molecular weight; Osteoporosis; Polymerase chain reaction; Proteins; Rats; Synoviocytes; Synoviocytes - metabolism; Tumor necrosis factor-α; Western blotting; collagen-induced arthritis; hyaluronidase; CEMIP; KIAA1199; hyaluronan; inflammatory arthritis
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms23084089

KIAA1199 has a strong hyaluronidase activity in inflammatory arthritis. This study aimed to identify a drug that could reduce KIAA1199 activity and clarify its effects on inflammatory arthritis. Rat chondrosarcoma (RCS) cells were strongly stained with Alcian blue (AB). Its stainability was reduced in RCS cells, which were over-expressed with the KIAA1199 gene (RCS-KIAA). We screened the drugs that restore the AB stainability in RCS-KIAA. The effects of the drug were evaluated by particle exclusion assay, HA ELISA, RT-PCR, and Western blotting. We further evaluated the HA accumulation and the MMP1 and three expressions in fibroblast-like synoviocytes (FLS). In vivo, the effects of the drug on symptoms and serum concentration of HA in a collagen-induced arthritis mouse were evaluated. Ipriflavone was identified to restore AB stainability at 23%. Extracellular matrix formation was significantly increased in a dose-dependent manner ( = 0.006). Ipriflavone increased the HA accumulation and suppressed the MMP1 and MMP3 expression on TNF-α stimulated FLS. In vivo, Ipriflavone significantly improved the symptoms and reduced the serum concentrations of HA. Conclusions: We identified Ipriflavone, which has inhibitory effects on KIAA1199 activity. Ipriflavone may be a therapeutic candidate based on its reduction of KIAA1199 activity in inflammatory arthritis.