Low-dose bortezomib increases the expression of NKG2D and DNAM-1 ligands and enhances induced NK and γδ T cell-mediated lysis in multiple myeloma

Oncotarget. 2017 Jan 24;8(4):5954-5964. doi: 10.18632/oncotarget.13979.

Abstract

Multiple myeloma (MM) is an incurable hematological malignancy, although bortezomib has markedly improved its outcomes. Growing clinical evidence indicates that enhancing induced natural killer (NK) or γδ T cells for infusion is useful in the treatment of MM. However, whether combination treatment with bortezomib and induced NK and γδ T cells further improves outcomes in MM, and how the treatments should be combined, remain unclear. Herein, we found that low-dose bortezomib did not suppress the viability of induced NK and γδ T cells, but did induce MM cell apoptosis. Importantly, low-dose bortezomib increased the expression of NKG2D and DNAM-1 ligands on MM cells, which sensitized the multiple myeloma cells to lysis by induced NK and γδ T cells. Our results suggested that combination treatment with low-dose bortezomib and induced NK or γδ T cells had a synergistic cytotoxic effect on MM cells. This study provided a proof of principle for the design of future trials and investigation of this combination therapeutic strategy for MM treatment.

Keywords: bortezomib; gamma-delta T cells; multiple myeloma; natural killer cells.

MeSH terms

  • Aged
  • Antigens, Differentiation, T-Lymphocyte / metabolism*
  • Antineoplastic Agents / pharmacology*
  • Bortezomib / pharmacology*
  • Cell Line, Tumor
  • Cell Survival
  • Combined Modality Therapy
  • Dose-Response Relationship, Drug
  • Female
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Intraepithelial Lymphocytes / cytology*
  • Intraepithelial Lymphocytes / drug effects
  • Intraepithelial Lymphocytes / transplantation
  • Killer Cells, Natural / cytology*
  • Killer Cells, Natural / drug effects
  • Killer Cells, Natural / metabolism
  • Killer Cells, Natural / transplantation
  • Ligands
  • Lymphocyte Activation / drug effects
  • Male
  • Middle Aged
  • Multiple Myeloma / metabolism*
  • Multiple Myeloma / therapy
  • NK Cell Lectin-Like Receptor Subfamily K / metabolism*
  • Up-Regulation

Substances

  • Antigens, Differentiation, T-Lymphocyte
  • Antineoplastic Agents
  • CD226 antigen
  • KLRK1 protein, human
  • Ligands
  • NK Cell Lectin-Like Receptor Subfamily K
  • Bortezomib