Development of novel therapeutic approaches for a bone disease in myeloma

 

Masahiro Abe

Department of Medicine and Bioregulatory Sciences

University of Tokushima Graduate School of Medicine

 

Myeloma cells stimulate bone resorption by enhancing osteoclast formation while suppressing bone formation. Macrophage inflammatory protein (MIP)-1a and MIP-1b as well as RANK ligand play a major role in the enhancement of bone resorption in myeloma. Myeloma cell-derived soluble Wnt inhibitors as well as TGF- b released from the bone through enhanced bone resorption suppress osteoblast differentiation. Such pathognomonically skewed cellular components in the bone marrow create a microenvironment suitable for myeloma cell growth and survival, which can be called as a “myeloma niche”. We need to target the myeloma niche to suppress myeloma expansion along with amelioration of bone lesions.