4.5 Review

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

期刊

BLOOD REVIEWS
卷 27, 期 6, 页码 261-267

出版社

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.blre.2013.08.002

关键词

Myeloma bone disease; DKK1; Antibody; Proteasome inhibitor; Vaccine

资金

  1. National Natural Science Foundation of China [81172257]
  2. Xi'an Fundamental Research Funds of China [HM1117-4]
  3. National Cancer Institute [RO1-CA90853]
  4. National Institutes of Health through the University of Texas MD Anderson Cancer Center Support Grant [CA016672]

向作者/读者索取更多资源

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.

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