德诺苏马布
组织蛋白酶K
硬骨素
骨质疏松症
骨吸收
破骨细胞
兰克尔
骨密度保护剂
骨重建
骨保护素
医学
代谢性骨病
细胞生物学
癌症研究
内科学
生物
骨矿物
受体
信号转导
激活剂(遗传学)
Wnt信号通路
出处
期刊:Drug research
[Thieme Medical Publishers (Germany)]
日期:2015-11-04
卷期号:65 (S 01): S14-S15
被引量:3
标识
DOI:10.1055/s-0035-1558064
摘要
Osteoporosis is a common disease characterised by a systemic impairment of bone mass and microarchitecture that results in fragility fractures. With an ageing population, the medical impact of osteoporosis will increase further. A detailed knowledge of bone biology with molecular insights into the communication between bone-forming osteoblasts and bone-resorbing osteoclasts and the orchestrating signalling network has led to the identification of novel therapeutic targets. Based on this, novel treatment strategies have been developed aimed at inhibiting excessive bone resorption and increasing bone formation. The most promising novel treatments include denosumab, a monoclonal antibody against receptor activator of NF-κB ligand, a key osteoclast cytokine, odanacatib, a specific inhibitor of the osteoclast protease cathepsin K, and antibodies against the sclerostin, an endogenous inhibitor of bone formation.
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