[Effect of ADAM10 Inhibitor GI254023X on Proliferation and Apoptosis of Multiple Myeloma H929 Cells and Its Possible Mechanisms]

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2015 Dec;23(6):1628-32. doi: 10.7534/j.issn.1009-2137.2015.06.019.
[Article in Chinese]

Abstract

Objective: To investigate the effect of ADAM10 inhibitor GI254023X on the proliferation and apoptosis of multiple myeloma H929 cell line and its mechanisms.

Methods: H929 cells were treated with different concentrations of GI254023X, the proliferation-inhibitive curve was assayed and plotted by CCK-8 method, the cell viability and apoptosis were detected by flow cytometry with Annexin V/7-AAD double staining. The cleavage of Notch1 protein (cleaved notch1) was determined by Western blot. The transcripts of Notch1 target gene Hes-1 were detected by real-time PCR.

Results: The GI254023X inhibited the proliferation of H929 cells in the time- and dose- dependent manners. As compared with the control group, the apoptosis of cells increased along with enhancement of GI254023X concentration; The expression of cleaved Notch1 was down-regulated after the treatment with GI254023X. The levels of Hes-1 mRNA transcripts in H929 cells was reduced in GI254023X treated group.

Conclusion: GI254023X can remarkably inhibit the proliferation and induce the apoptosis of H929 cells. Its mechanism may be associated with inbihition of Notch1 activation.

MeSH terms

  • ADAM Proteins
  • ADAM10 Protein
  • Amyloid Precursor Protein Secretases
  • Apoptosis*
  • Cell Line, Tumor
  • Cell Proliferation
  • Dipeptides
  • Down-Regulation
  • Humans
  • Hydroxamic Acids
  • Membrane Proteins
  • Multiple Myeloma*
  • Receptor, Notch1

Substances

  • 3-(formylhydroxyamino)-2-(3-phenyl-1-propyl)butanoic acid (2,2-dimethyl-1-methylcarbamoyl-1-propyl)amide
  • Dipeptides
  • Hydroxamic Acids
  • Membrane Proteins
  • NOTCH1 protein, human
  • Receptor, Notch1
  • Amyloid Precursor Protein Secretases
  • ADAM Proteins
  • ADAM10 Protein
  • ADAM10 protein, human