Dickkopf-1 is a key regulator of myeloma bone disease: Opportunities and challenges for therapeutic intervention

被引:44
作者
Zhou, Fuling [1 ,2 ]
Meng, Shan [1 ]
Song, Huanjin [3 ]
Claret, Francois X. [2 ,4 ,5 ]
机构
[1] Xi An Jiao Tong Univ, Dept Clin Hematol, Affiliated Hosp 2, Xian 710004, Peoples R China
[2] Univ Texas MD Anderson Canc Ctr, Unit 0950, Dept Syst Biol, Houston, TX 77030 USA
[3] Xi An Jiao Tong Univ, Dept Orthopaed, Affiliated Hosp 2, Xian 710004, Peoples R China
[4] Univ Texas Houston, Grad Sch Biomed Sci Houston, Expt Therapeut Acad Program, Houston, TX 77030 USA
[5] Univ Texas Houston, Grad Sch Biomed Sci Houston, Canc Biol Program, Houston, TX 77030 USA
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
Myeloma bone disease; DKK1; Antibody; Proteasome inhibitor; Vaccine; MARROW STROMAL CELLS; MESENCHYMAL STEM-CELLS; MULTIPLE-MYELOMA; OSTEOBLAST DIFFERENTIATION; SERUM CONCENTRATIONS; IN-VIVO; HEAD INDUCTION; WNT INHIBITOR; DKK1; EXPRESSION;
D O I
10.1016/j.blre.2013.08.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Myeloma bone disease (MBD) is the most visible aspect of plasma cell myeloma (PCM), which is characterized by the displacement of hematopoiesis and the formation of osteolytic bone lesions. The secreted glycoprotein Dickkopf-1 (DKK1), an inhibitor of the Wnt signaling pathway, is broadly expressed in myeloma cells but highly restricted in normal tissues. DKK1 plays a critical role in several aspects of bone biology and actively participates in regulating MBD by inhibiting osteoblasts and by activating osteoclasts. Based on these findings, ongoing research has been targeting DKK1 to find novel therapeutic strategies for MBD, such as DIM-neutralizing antibodies, proteasome inhibitors, and vaccines. All these strategies have produced encouraging clinical results and consequently, revealed the significance of DKK1 in MBD. This review discusses the recent advances in our understanding of the DIM pathway signaling and how DIM can be exploited in the therapeutic intervention of MBD. Published by Elsevier Ltd.
引用
收藏
页码:261 / 267
页数:7
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