2025/10/17 by Cheng Peng, Zixiang Geng, Zhe Jiang +7
Biochemistry, Genetics and Molecular Biology · Medicine · #Bone Metabolism and Diseases #Estrogen and related hormone effects #Bone health and treatments
paper · doi:10.1021/acs.jmedchem.5c01697
Osteoporosis is a systemic and chronic metabolic bone disease of high fracture and mortality. Simultaneous regulation of osteoblast-mediated bone formation and osteoclast-mediated bone resorption has become a potentially effective therapeutic strategy to overcome osteoporosis. Recently, selective activation of estrogen receptor β (SERβ) was demonstrated to promote osteoblast formation and inhibit osteoclast absorption, suggesting that SERβ agonists may be another promising therapeutic approach for treating osteoporosis. Herein, we reported the discovery of a bisphosphonate indanone compound ( S )-STO021 as a novel SERβ agonist, which exhibited excellent dual functional effects of inhibiting osteoclast resorption and promoting osteoblast formation. Mechanically, the antiosteoporosis efficacy of ( S )-STO021 was achieved through inhibiting the TAK1/MKK6/p38 signal and promoting the ERβ/BMP4/SMAD signal. Furthermore, ( S )-STO021 could not only effectively improve the zebrafish osteoporosis model induced by glucocorticoids but also greatly restore the bone microstructure in ovariectomized rat models. Collectively, our SERβ agonist ( S )-STO021 could regulate osteoblast and osteoclast differentiation, showing the potential to treat osteoporosis.