[Effects of proteasome inhibitor PS-341 on the multiple cytokine expressions of mesenchymal stem cells from bone marrow in patients with multiple myeloma]

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2006 Feb;14(1):61-4.
[Article in Chinese]

Abstract

To explore the effects of proteasome inhibitor PS-341 on the cytokine expressions of mesenchymal stem cells (MSC) in patients with multiple myeloma (MM), MSCs of 11 patients were cultured in medium of RPMI 1640 containing 10% FBS. When cells grew to 5 x 10(5) - 1 x 10(6), cells were exposed to 50 nmol/L PS-341 for 4 hours, then harvested. The expressions of IL-6, IL-1beta and SCF were detected by RT-PCR. The results indicated that after treatment with PS-341 the expressions of IL-6, IL-1beta and SCF of MSCs decreased markedly, especially that of IL-1beta, compared with control (P < 0.05, P < 0.01, P < 0.05, respectively). There were obviously differences of IL-1beta expression between refractory/relapsed group and complete remission (CR) group and IL-1beta expression was inhibited more seriously in CR group, whereas there were no significant differences of IL-6 and SCF expression between two groups; IL-1beta expression of patients treated with PS-341 was not detected; there were not effects of IL-1beta expression on expressions of IL-6 and SCF. It is concluded that proteasome inhibitor PS-341 downregulated the expressions of IL-6, IL-1beta and SCF of MSCs in patients with MM.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Bone Marrow Cells / metabolism*
  • Bone Marrow Cells / pathology
  • Boronic Acids / pharmacology*
  • Bortezomib
  • Cytokines / biosynthesis*
  • Humans
  • Interleukin-1beta / biosynthesis
  • Interleukin-6 / biosynthesis
  • Mesenchymal Stem Cells / metabolism*
  • Multiple Myeloma / metabolism*
  • Multiple Myeloma / pathology
  • Protease Inhibitors / pharmacology
  • Pyrazines / pharmacology*
  • Stem Cell Factor / biosynthesis

Substances

  • Antineoplastic Agents
  • Boronic Acids
  • Cytokines
  • Interleukin-1beta
  • Interleukin-6
  • Protease Inhibitors
  • Pyrazines
  • Stem Cell Factor
  • Bortezomib