Evidence of a role for RANKL in the development of myeloma bone disease

被引：20

作者：

De Leenheer, E

Mueller, GS

Vanderkerken, K

Croucher, PI

机构：

[1] Univ Sheffield, Sch Med, Bone Biol Grp, Div Clin Sci, Sheffield S10 2RX, S Yorkshire, England

[2] Univ Oxford, Botnar Res Ctr, Nuffield Dept Orthopaed Surg, Oxford, England

[3] Free Univ Brussels, Dept Hematol & Immunol, Brussels, Belgium

来源：

CURRENT OPINION IN PHARMACOLOGY | 2004年 / 4卷 / 04期

关键词：

D O I：

10.1016/j.coph.2004.03.011

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

Multiple myeloma is associated with the development of a devastating bone disease mediated by increased osteoclastic activity. The ligand for receptor activator of nuclear factor-kappaB (RANKL) plays a critical role in normal osteoclast biology and is abnormally regulated in myeloma. Targeting this system with recombinant decoy receptor, osteoprotegerin, or soluble forms of the receptor activator of nuclear factor-kappaB is able to prevent myeloma bone disease in pre-clinical models. Intriguingly, inhibiting osteoclast formation and bone resorption, and altering the bone marrow microenvironment, results in an indirect anti-myeloma effect.

引用

收藏

页码：340 / 346

页数：7

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