[Study on the biological activity and molecular mechanism of IFNalpha on human myeloma cell line Sko-007]

Zhonghua Xue Ye Xue Za Zhi. 2002 Oct;23(10):517-9.
[Article in Chinese]

Abstract

Objective: To investigate the biological activity and molecular mechanism of interferon alpha (IFNalpha) on human myeloma cell line Sko-007.

Methods: The effect of IFNalpha on the growth of Sko-007 cells was measured by MTT assay. Cells cycle distribution and the expression of two IL-6 receptor chains (IL-6R and gp130) on Sko-007 cell surface in the absence or presence of IFNalpha were monitored by FACS analysis. The activation state of protein kinase ERK, which is involved in Ras/MAPK signal transduction pathway mediating cell survival and proliferation, and the expression of anti-apoptotic Bcl-2 family proteins-Bcl-2, Bcl-x(L) and Mcl-1 in Sko-007 cells with or without IFNalpha were determined by immunoblot assay.

Result: IFNalpha arrested Sko-007 cell cycle progression. After stimulation with IFNalpha, an obvious increase in G(0)/G(1) phase (41.1%-->84.1%) and decrease in S phase (57.1%-->13.3%) of Sko-007 cell cycle distribution can be observed. Moreover, the proliferation of Sko-007 cells was dramatically inhibited in the presence of IFNalpha, with a maximal inhibitory rate up to 88%. In addition, the expression of gp130 on cell surface, the activation of protein kinase ERK and the expression of Bcl-2 and Bcl-x(L) were all down-regualted in IFNalpha-stimulated Sko-007 cells.

Conclusion: The inhibitory effect of IFNalpha on the proliferation of Sko-007 cells was mediated by gp130 down-regulation, degradation of Bcl-2 family anti-apoptotic proteins and inhibition of ERK activation.

MeSH terms

  • Antigens, CD / drug effects
  • Antigens, CD / metabolism
  • Cell Cycle / drug effects
  • Cell Division / drug effects
  • Cytokine Receptor gp130
  • Dose-Response Relationship, Drug
  • Down-Regulation
  • Enzyme Activation / drug effects
  • G1 Phase / drug effects
  • Humans
  • Immunoblotting
  • Interferon-alpha / pharmacology*
  • Membrane Glycoproteins / drug effects
  • Membrane Glycoproteins / metabolism
  • Mitogen-Activated Protein Kinases / metabolism
  • Multiple Myeloma / metabolism
  • Multiple Myeloma / pathology*
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Receptors, Interleukin-6 / drug effects
  • Receptors, Interleukin-6 / metabolism
  • Resting Phase, Cell Cycle / drug effects
  • S Phase / drug effects
  • Tumor Cells, Cultured / drug effects
  • Tumor Cells, Cultured / metabolism
  • bcl-X Protein

Substances

  • Antigens, CD
  • BCL2L1 protein, human
  • IL6ST protein, human
  • Interferon-alpha
  • Membrane Glycoproteins
  • Proto-Oncogene Proteins c-bcl-2
  • Receptors, Interleukin-6
  • bcl-X Protein
  • Cytokine Receptor gp130
  • Mitogen-Activated Protein Kinases