Inhibition of Cathepsin K for Treatment of Osteoporosis

被引:116
作者
Boonen, Steven [1 ,2 ]
Rosenberg, Elizabeth [3 ]
Claessens, Frank [4 ]
Vanderschueren, Dirk [5 ]
Papapoulos, Socrates [6 ]
机构
[1] Leuven Univ, Div Geriatr Med, B-3000 Leuven, Belgium
[2] Ctr Metab Bone Dis, B-3000 Leuven, Belgium
[3] Merck Sharp & Dohme Corp, Whitehouse Stn, NJ USA
[4] Leuven Univ, Dept Mol Cell Biol, B-3000 Leuven, Belgium
[5] Leuven Univ, Dept Androl & Endocrinol, B-3000 Leuven, Belgium
[6] Leiden Univ, Med Ctr, Leiden, Netherlands
关键词
Cathepsin K inhibition; Osteoporosis; BONE-MINERAL DENSITY; POSTMENOPAUSAL WOMEN; RESORPTION; TURNOVER; EFFICACY; ONO-5334; PYCNODYSOSTOSIS; OSTEOPETROSIS; DEGRADATION; OSTEOCLASTS;
D O I
10.1007/s11914-011-0085-9
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Cathepsin K is the protease that is primarily responsible for the degradation of bone matrix by osteoclasts. Inhibitors of cathepsin K are in development for treatment of osteoporosis. Currently available antiresorptive drugs interfere with osteoclast function. They inhibit both bone resorption and formation, due to the coupling between these processes. Cathepsin K inhibitors, conversely, target the resorption process itself and may not interfere with osteoclast stimulation of bone formation. In fact, when cathepsin K is absent or inhibited in mice, rabbits, or monkeys, bone formation is maintained or increased. In humans, inhibition of cathepsin K is associated with sustained reductions in bone resorption markers but with smaller and transient reductions in bone formation markers. The usefulness of cathepsin K inhibitors in osteoporosis is now being examined in phase 2 and phase 3 clinical trials of postmenopausal osteoporotic women.
引用
收藏
页码:73 / 79
页数:7
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