Inhibition of the ubiquitin-proteasome pathway activates stress kinases and induces apoptosis in renal cancer cells

Int J Oncol. 2004 Sep;25(3):697-702.

Abstract

The ubiquitin-proteasome pathway plays a critical role in the degradation of cellular proteins related to signal transduction. Cytokine and growth factor-dependent aberrant proliferation has been implicated in renal cell carcinoma (RCC). We hypothesized that inhibiting the proteasome function might activate a proapoptotic signal transduction by modulating the cytokine and growth factor related signal transduction pathway. We therefore investigated the effectiveness of a proteasome inhibitor in the treatment of RCC regarding the involvement of Mitogen-activated protein kinases (MAP kinases), because MAP kinases are major signal transduction molecules that are known to play a pivotal role in cancer cell proliferation or apoptosis triggered by extra-cellular cytokines and growth factors. A proteasome inhibitor, MG132 inhibited the proliferation of RCC cell lines, 786-O and KU20-01 in a time and dose-dependent manner. 786-O cells have truncated von-Hippel Lindau (VHL) tumor suppressor gene protein due to a one base pair deletion at exon 1, whereas KU20-01 cells have a wild-type VHL protein. MG132 induced apoptosis in both cell lines. The inhibition of the ubiquitin-proteasome pathways was confirmed by the accumulation of ubiquitin-tagged proteins. MG132 induced the phosphorylation of ERK at 4 h and thereafter persisted for 8 to 16 h. In contrast, JNK and p38 activation persisted for longer periods and remained enhanced until 24 h. The concomitant activation of effector caspases, caspase-3 and caspase-7 was observed in 786-O cells. The inhibition of the proteasome function can induce apoptosis in RCC irrespective of the VHL protein status. The persistence of JNK and p38 activation may therefore be a unique mechanism underlying MG132 induced apoptosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis*
  • Carcinoma, Renal Cell / enzymology*
  • Carcinoma, Renal Cell / metabolism
  • Caspase 3
  • Caspase 7
  • Caspases / metabolism
  • Cell Line, Tumor
  • Humans
  • Kidney Neoplasms / enzymology*
  • Kidney Neoplasms / metabolism
  • Leupeptins / pharmacology
  • Mitogen-Activated Protein Kinases / metabolism*
  • Proteasome Inhibitors*
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Ubiquitins / metabolism*
  • bcl-X Protein

Substances

  • BCL2L1 protein, human
  • Leupeptins
  • Proteasome Inhibitors
  • Proto-Oncogene Proteins c-bcl-2
  • Ubiquitins
  • bcl-X Protein
  • Mitogen-Activated Protein Kinases
  • CASP3 protein, human
  • CASP7 protein, human
  • Caspase 3
  • Caspase 7
  • Caspases
  • benzyloxycarbonylleucyl-leucyl-leucine aldehyde