Literature DB >> 21814021

[Myeloma bone disease and RANKL signaling].

Masahiro Abe1.   

Abstract

Multiple myeloma develops and expands almost exclusively in the bone marrow, and generates devastating bone destruction. Myeloma cells produce a variety of cytokines including MIP-1 to stimulate bone resorption by enhancing RANKL expression, and suppress bone formation by inhibiting osteoblast differentiation, leading to bone destruction and rapid loss of bone. The emerging role of the RANKL/RANK signaling axis provide a molecular rationale for consideration of targeting RANKL/RANK in a bone disease in myeloma. Given formation of vicious cycle between bone destruction and tumor progression, inhibiting RANKL signaling may also contribute to the suppression of myeloma expansion.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21814021     DOI: CliCa110811671174

Source DB:  PubMed          Journal:  Clin Calcium        ISSN: 0917-5857


  2 in total

Review 1.  Reconstruction of multiple myeloma lesions around the pelvis and acetabulum.

Authors:  Vasileios I Sakellariou; Andreas F Mavrogenis; Olga Savvidou; Franklin H Sim; Panayiotis J Papagelopoulos
Journal:  Eur J Orthop Surg Traumatol       Date:  2014-10-19

2.  Bone marrow stromal cells derived MCP-1 reverses the inhibitory effects of multiple myeloma cells on osteoclastogenesis by upregulating the RANK expression.

Authors:  Zhiqiang Liu; Jingda Xu; Haiyan Li; Yuhuan Zheng; Jin He; Huan Liu; Yuping Zhong; Yong Lu; Bangxing Hong; Mingjun Zhang; Pei Lin; Juan Du; Jian Hou; Jianfei Qian; Larry W Kwak; Qing Yi; Jing Yang
Journal:  PLoS One       Date:  2013-12-10       Impact factor: 3.240

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.