Apoptotic effect of MG-132 on human tongue squamous cell carcinoma

Biomed Pharmacother. 2011 Aug;65(5):322-7. doi: 10.1016/j.biopha.2011.04.009. Epub 2011 Jun 12.

Abstract

The aim of this study was to investigate the apoptotic effect of a proteasome inhibitor MG-132 on Tca-8113, a cell line of human tongue squamous cell carcinoma. Tca-8113 cells were treated with 10, 20, and 30μM of MG-132, or 5μM thapsigargin. Apoptosis rate was determined with annexin V/propidium iodide double staining. Expression of E3ubiquitin-protein ligase was determined by ELISA, and Grp78 and caspase-12 mRNA, and Grp78 and caspase-12 protein was assessed by RT-PCR and Western blot, respectively. Apoptosis was observed 18h after MG-132 treatment. The apoptotic rate in the 10, 20, and 30μM MG-132 group was 13.5, 19.6 and 34.7%, respectively, which was higher than in the thapsigargin (8.5%, P<0.01) or control group (0.5%, P<0.01). The expression of E3 ubiquitin-protein ligase in the 10, 20, and 30μM MG-132 group was 28.75±2.28, 18.16±0.65, 8.85±0.72, respectively, which was lower than in the thapsigargin (38.96±0.33, P<0.05 or 0.01) or control (40.88±4.52, P<0.05 or 0.01) group. The levels of Grp78 and capase-12 mRNA, Grp78 and caspase-12 protein in the MG-132 groups were higher than in the control group (P<0.01). In conclusion, MG-132 induces apoptosis in Tca-8113 cells in a concentration-dependent manner. The MG-132-induced apoptosis may involve downregulation of E3 ubiquitin ligase, and upregulation of Grp78 and caspase-12.

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Apoptosis / drug effects*
  • Carcinoma, Squamous Cell / drug therapy*
  • Carcinoma, Squamous Cell / enzymology
  • Carcinoma, Squamous Cell / genetics
  • Carcinoma, Squamous Cell / pathology
  • Caspase 12 / biosynthesis
  • Caspase 12 / genetics
  • Caspase 12 / metabolism
  • Cell Line, Tumor
  • Cysteine Proteinase Inhibitors / pharmacology
  • Endoplasmic Reticulum Chaperone BiP
  • Heat-Shock Proteins / biosynthesis
  • Heat-Shock Proteins / genetics
  • Heat-Shock Proteins / metabolism
  • Humans
  • Leupeptins / pharmacology*
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Thapsigargin / pharmacology
  • Tongue Neoplasms / drug therapy*
  • Tongue Neoplasms / enzymology
  • Tongue Neoplasms / genetics
  • Tongue Neoplasms / pathology
  • Ubiquitin-Protein Ligases / biosynthesis
  • Ubiquitin-Protein Ligases / genetics
  • Ubiquitin-Protein Ligases / metabolism

Substances

  • Antineoplastic Agents
  • Cysteine Proteinase Inhibitors
  • Endoplasmic Reticulum Chaperone BiP
  • HSPA5 protein, human
  • Heat-Shock Proteins
  • Leupeptins
  • RNA, Messenger
  • Thapsigargin
  • Ubiquitin-Protein Ligases
  • Caspase 12
  • benzyloxycarbonylleucyl-leucyl-leucine aldehyde