Up-regulated EGF receptors undergo to rapid internalization and ubiquitin-dependent degradation in human cancer cells exposed to 8-Cl-cAMP

M. Caraglia, E. Di Gennaro, D. Barbarulo, M. Marra, P. Tagliaferri, A. Abbruzzese, A. Budillon

Research output: Contribution to journalArticlepeer-review

Abstract

8-Cl-cAMP, a cAMP analogue that antagonizes type I cAMP-dependent protein kinase, is a novel anti-tumor agent presently under investigation in clinical trials. Herein we report the effects of this agent on epidermal growth factor receptor expression and degradation in human KB cancer cells. Exposure to 10 μM 8-Cl-cAMP for 48 h induced a 65% increase in epidermal growth factor receptor surface expression while the receptor synthesis was 22-fold enhanced. Analysis of epidermal growth factor-dependent receptor internalization in 8-Cl-cAMP-treated cells showed a higher endocytosis rate as well as an accelerated degradation which occurred together with an increased receptor ubiquitination. The enhanced degradation of epidermal growth factor receptor correlated with the lack of epidermal growth factor-induced proliferation and mitogen-activated protein kinase stimulation. The disregulation of epidermal growth factor receptor internalization and ubiquitin-dependent degradation could underlay a new mechanism of the anti-tumor activity of 8-Cl-cAMP suggesting its combination with agents that disrupt epidermal growth factor receptor signalling. Copyright (C) 1999 Federation of European Biochemical Societies.

Original languageEnglish
Pages (from-to)203-208
Number of pages6
JournalFEBS Letters
Volume447
Issue number2-3
DOIs
Publication statusPublished - Mar 26 1999

Keywords

  • cAMP analogue
  • Endocytosis
  • Epidermal growth factor receptor
  • Mitogen-activated protein kinase
  • Protein kinase A
  • Ubiquitin

ASJC Scopus subject areas

  • Biochemistry
  • Biophysics
  • Molecular Biology

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