Lycorine targets multiple myeloma stem cell-like cells by inhibition of Wnt/β-catenin pathway

Br J Haematol. 2020 Jun;189(6):1151-1164. doi: 10.1111/bjh.16477. Epub 2020 Mar 13.

Abstract

Multiple myeloma (MM) is characterised by the proliferation and accumulation of malignant plasma cells in the bone marrow. Despite the progress in treatment over the last few years, MM remains incurable and the majority of patients relapse. MM stem-like cells (MMSCs) have been considered as the main reason for drug resistance and eventual relapse. Currently, therapeutic agents are not enough to eradicate MMSCs, and finding effective strategies to eradicate MMSCs may improve the outcome of patients. Here we showed that lycorine, a natural compound from the Amaryllidaceae species, effectively inhibits the proliferation of myeloma cells from cell lines or patients, mainly through decreasing ALDH1+ cells. Mechanistically, lycorine decreases the MMSC population through inhibition of the Wnt/β-catenin pathway by reducing the β-catenin protein level. Moreover, lycorine could overcome the increasing proportion of ALDH1+ cells caused by bortezomib (BTZ) treatment, and a combination BTZ and lycorine have a synergistic effect on anti-myeloma cells. Furthermore, we found a similar reduction of MMSC characteristics by lycorine in BTZ-resistant MM cells and primary CD138+ plasma cells. Collectively, our findings indicate lycorine as a promising agent to target MMSCs to overcome the drug resistance of BTZ, and that, alone or in combination with BTZ, lycorine is a potential therapeutic strategy for MM treatments.

Keywords: Wnt/β-catenin pathway; multiple myeloma; stem cell-like cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amaryllidaceae Alkaloids / pharmacology*
  • Cell Line, Tumor
  • Humans
  • Multiple Myeloma* / drug therapy
  • Multiple Myeloma* / metabolism
  • Multiple Myeloma* / pathology
  • Neoplasm Proteins / metabolism*
  • Neoplastic Stem Cells* / metabolism
  • Neoplastic Stem Cells* / pathology
  • Phenanthridines / pharmacology*
  • Wnt Signaling Pathway / drug effects*
  • beta Catenin / metabolism*

Substances

  • Amaryllidaceae Alkaloids
  • CTNNB1 protein, human
  • Neoplasm Proteins
  • Phenanthridines
  • beta Catenin
  • lycorine