Key roles of the OPG-RANK-RANKL system in bone oncology

被引:68
作者
Baud'huin, M.
Duplomb, L.
Velasco, C. Ruiz
Fortun, Y.
Heymann, D.
Padrines, M.
机构
[1] Univ Nantes, Nantes Atlantique Univ, Lab Physiopathol Resorpt Osseuse & Therapie Tumeu, Nantes, France
[2] INSERM, ERI7, F-44035 Nantes, France
关键词
bone; metastases; OPG; osteoblast; osteoclast; osteolysis; primary tumor; RANKL; secondary tumor;
D O I
10.1586/14737140.7.2.221
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osteoprotegerin (OPG)-receptor activator of nuclear factor-kappa B (RANK) and RANK ligand (RANKL) have been identified as members of a ligand-receptor system that directly regulates osteoclast differentiation and osteolysis. RANKL may be a powerful inducer of bone resorption through its interaction with RANK, and OPG is a soluble decoy receptor that acts as a strong inhibitor of osteoclastic differentiation. Any dysregulation of their respective expression leads to pathological conditions. Furthermore, recent data demonstrate that the OPG-RANK-RANKL system modulates cancer cell migration, thus controlling the development of bone metastases. This review describes the most recent knowledge on the OPG-RANK-RANKL system, its involvement in bone oncology and the new therapeutic approaches based on this molecular triad.
引用
收藏
页码:221 / 232
页数:12
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