Oncogenic signals of HER-2/neu in regulating the stability of the cyclin-dependent kinase inhibitor p27

J Biol Chem. 2000 Aug 11;275(32):24735-9. doi: 10.1074/jbc.C000147200.

Abstract

Overexpression and activation of HER-2/neu, a proto-oncogene, play a pivotal role in cancer formation. Strong expression of HER-2/neu in cancers has been associated with poor prognosis. Reduced expression of p27(Kip1), a cyclin-dependent kinase inhibitor, correlates with poor clinical outcome in many types of carcinomas. Because many cancers with the overexpression of HER-2/neu overlap with those affected by reduced p27 expression, we studied the link between HER-2/neu oncogenic signals and p27 regulation. We found that down-regulation of p27 correlates with HER-2/neu overexpression. To address the molecular mechanism of this inverse correlation, we found that reduction of p27 is caused by enhanced ubiquitin-mediated degradation, and the HER-2/Grb2/MAPK pathway is involved in the decrease of p27 stability. Also, HER-2/neu activity causes mislocation of p27 and Jun activation domain-binding protein 1 (JAB1), an exporter of p27, into the cytoplasm, thereby facilitating p27 degradation. These results reveal that HER-2/neu signals reduce p27 stability and thus present potential points for therapeutic intervention in HER-2/neu-associated cancers.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • 3T3 Cells
  • Animals
  • Cell Cycle Proteins*
  • Cell Line
  • Cyclin-Dependent Kinase Inhibitor p27
  • Cyclin-Dependent Kinases / antagonists & inhibitors*
  • Genes, erbB-2*
  • Humans
  • Kinetics
  • Mice
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / metabolism*
  • Mitogen-Activated Protein Kinases / metabolism
  • Models, Biological
  • Protein Kinases / metabolism
  • Proto-Oncogene Mas
  • Receptor, ErbB-2 / genetics*
  • Receptor, ErbB-2 / metabolism*
  • Recombinant Proteins / metabolism
  • Signal Transduction
  • Transfection
  • Tumor Suppressor Proteins*
  • Ubiquitins / metabolism

Substances

  • Cdkn1b protein, mouse
  • Cell Cycle Proteins
  • MAS1 protein, human
  • Microtubule-Associated Proteins
  • Proto-Oncogene Mas
  • Recombinant Proteins
  • Tumor Suppressor Proteins
  • Ubiquitins
  • Cyclin-Dependent Kinase Inhibitor p27
  • Protein Kinases
  • histone H1 kinase
  • Receptor, ErbB-2
  • Cyclin-Dependent Kinases
  • Mitogen-Activated Protein Kinases