NF-κB localization in multiple myeloma plasma cells and mesenchymal cells

Leuk Res. 2011 Jan;35(1):52-60. doi: 10.1016/j.leukres.2010.06.023. Epub 2010 Jul 31.

Abstract

Several reports demonstrated that the activation of Nuclear Factor-kappa B NF-κB is essential for the pathogenesis of multiple myeloma (MM). We analyzed the nuclear localization of NF-κB in MM-cells derived from 60 different patients with MM at presentation and in relapse, as well as in three myeloma cell lines. Nuclear localization (the active form) of NF-κB was detected in only one MM-sample from a refractory patient and in two samples from relapsed patients, while all the other samples, including the MM-cell lines, almost exclusively express the cytoplasmic (inactive) form of NF-κB. In mesenchymal cells from MM-patients NF-κB was clearly present in the nucleus. In addition, the proteasome inhibitor Bortezomib, which is described to antagonize NF-κB activity, had a consistent antitumor activity against both chemoresistant and chemosensitive MM-cells, regardless the NF-κB localization, thus suggesting the existence of other molecular targets of proteasome inhibitors in MM.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Blotting, Western
  • Boronic Acids / pharmacology
  • Bortezomib
  • Cell Line, Tumor
  • Flow Cytometry
  • Humans
  • Immunohistochemistry
  • Mesoderm / metabolism*
  • Mesoderm / pathology
  • Multiple Myeloma / metabolism*
  • Multiple Myeloma / pathology
  • NF-kappa B / metabolism*
  • Plasma Cells / metabolism*
  • Pyrazines / pharmacology

Substances

  • Antineoplastic Agents
  • Boronic Acids
  • NF-kappa B
  • Pyrazines
  • Bortezomib