Therapeutic targeting of osteoclast function and pathways

被引:56
作者
Broadhead, Matthew L. [1 ,2 ]
Clark, Jonathan C. M. [1 ,2 ]
Dass, Crispin R. [4 ]
Choong, Peter F. M. [1 ,2 ,3 ]
Myers, Damian E. [1 ,2 ]
机构
[1] St Vincents Hosp, Dept Orthopaed, Fitzroy, Vic 3065, Australia
[2] Univ Melbourne, Dept Surg, Fitzroy, Vic 3065, Australia
[3] Peter MacCallum Canc Ctr, Sarcoma Serv, Melbourne, Vic, Australia
[4] Victoria Univ, Sch Biomed & Hlth Sci, St Albans, Vic, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
bone metastases; osteoclast; osteoporosis; osteosarcoma; rheumatoid arthritis; FACTOR-KAPPA-B; GIANT-CELL TUMOR; SOLUBLE RECEPTOR ACTIVATOR; BONE-MINERAL DENSITY; NUCLEAR-FACTOR; RHEUMATOID-ARTHRITIS; BREAST-CANCER; IN-VITRO; OSTEOPROTEGERIN LIGAND; DIFFERENTIATION FACTOR;
D O I
10.1517/14728222.2011.546351
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Introduction: Osteoclasts are responsible for bone resorption and underlie a number of pathological states in which osteolysis is a feature. Over recent decades our molecular understanding of osteoclast differentiation and activation has expanded significantly, and this has allowed for the development of a number of osteoclast-targeted therapies. Areas covered: This review seeks to present the underlying molecular mechanisms of osteoclast differentiation and activity as a basis for understanding our current treatment of osteoporosis and malignant tumors in bone. Osteoclast-targeted therapies are also being evaluated for the treatment of rheumatoid arthritis, osteosarcoma and giant cell tumor of bone. Expert opinion: With concurrent advances in the fields of molecular biology, pathology and advanced imaging, osteoclast-targeted therapies show great potential for treating conditions in which excess resorption of bone is a key pathological process. Targeting of osteoclast control mechanisms offers the potential of combining 'molecular imaging' with therapeutic intervention and longitudinal monitoring of disease processes.
引用
收藏
页码:169 / 181
页数:13
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