St. Vincent's Hospital, Department of Orthopaedics and University of Melbourne, Department of Surgery, L3, Daly Wing, 35 Victoria Parade, Fitzroy 3065, VIC, Australia.
Expert Opin Ther Targets. 2011 Feb;15(2):169-81. doi: 10.1517/14728222.2011.546351. Epub 2011 Jan 5.
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.
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.
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.
破骨细胞负责骨吸收,是许多骨质溶解为特征的病理状态的基础。近几十年来,我们对破骨细胞分化和激活的分子理解有了显著的扩展,这使得许多针对破骨细胞的治疗方法得以发展。
本文旨在介绍破骨细胞分化和活性的潜在分子机制,作为理解我们目前治疗骨质疏松症和骨恶性肿瘤的基础。针对破骨细胞的治疗方法也在评估用于治疗类风湿关节炎、骨肉瘤和骨巨细胞瘤。
随着分子生物学、病理学和先进成像领域的同步发展,针对破骨细胞的治疗方法在治疗骨质过度吸收这一关键病理过程的疾病方面显示出巨大的潜力。针对破骨细胞控制机制的靶向治疗有可能将“分子成像”与治疗干预和疾病过程的纵向监测相结合。