DKK1 suppresses WWP2 to enhance bortezomib resistance in multiple myeloma via regulating GLI2 ubiquitination

Carcinogenesis. 2021 Oct 26;42(10):1223-1231. doi: 10.1093/carcin/bgab086.

Abstract

Bortezomib-based chemotherapy represents the most prevalent regimens for multiple myeloma (MM), whereas acquired drug resistance remains a major obstacle. Myeloma cells often produce excessive amount of dickkopf-1 (DKK1), giving rise to myeloma bone disease. However, it remains obscure about the effects and mechanisms of DKK1 in the progression and bortezomib responsiveness of MM cells. In the current study, we found WWP2, an E3 ubiquitin-protein ligase, was downregulated in the bortezomib-resistant cells along with high expression of DKK1. Further investigation revealed that WWP2 was a direct target of Wnt/β-catenin signaling pathway, and DKK1 suppressed the expression of WWP2 via canonical Wnt signaling. We further identified that WWP2 mediated the ubiquitination and degradation of GLI2, a main transcriptional factor of the Hedgehog (Hh) pathway. Therefore, DKK1-induced WWP2 downregulation improved GLI2 stability and activation of Hh signaling pathway, contributing to the resistance to bortezomib of MM cells. Clinical data also validated that WWP2 expression was associated with the treatment response and clinic outcomes of MM patients. WWP2 overexpression restricted MM progression and enhanced cell sensitivity to bortezomib treatment in vitro and in vivo. Taken together, our findings demonstrate that DKK1 facilitates the generation of bortezomib resistance in MM via downregulating WWP2 and activating Hh pathway. Thus, the manipulation of DKK1-WWP2-GLI2 axis might sensitize myeloma cells to proteasome inhibitors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / therapeutic use*
  • Bortezomib / therapeutic use*
  • Cell Line, Tumor
  • Drug Resistance, Neoplasm / physiology*
  • HEK293 Cells
  • Humans
  • Intercellular Signaling Peptides and Proteins / physiology*
  • Multiple Myeloma / drug therapy*
  • Multiple Myeloma / metabolism
  • Nuclear Proteins / metabolism*
  • Treatment Outcome
  • Ubiquitin-Protein Ligases / genetics*
  • Ubiquitin-Protein Ligases / physiology
  • Ubiquitination
  • Wnt Signaling Pathway
  • Zinc Finger Protein Gli2 / metabolism*

Substances

  • Antineoplastic Agents
  • DKK1 protein, human
  • GLI2 protein, human
  • Intercellular Signaling Peptides and Proteins
  • Nuclear Proteins
  • Zinc Finger Protein Gli2
  • Bortezomib
  • WWP2 protein, human
  • Ubiquitin-Protein Ligases