| Literature DB >> 17486068 |
K Shtiegman1, B S Kochupurakkal, Y Zwang, G Pines, A Starr, A Vexler, A Citri, M Katz, S Lavi, Y Ben-Basat, S Benjamin, S Corso, J Gan, R B Yosef, S Giordano, Y Yarden.
Abstract
Several distinct mutations within the kinase domain of the epidermal growth factor receptor (EGFR) are associated with non-small cell lung cancer, but mechanisms underlying their oncogenic potential are incompletely understood. Although normally ligand-induced kinase activation targets EGFR to Cbl-mediated receptor ubiquitinylation and subsequent degradation in lysosomes, we report that certain EGFR mutants escape this regulation. Defective endocytosis characterizes a deletion mutant of EGFR, as well as a point mutant (L858R-EGFR), whose association with c-Cbl and ubiquitinylation are impaired. Our data raise the possibility that refractoriness of L858R-EGFR to downregulation is due to enhanced heterodimerization with the oncogene product HER2, which leads to persistent stimulation.Entities:
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Year: 2007 PMID: 17486068 DOI: 10.1038/sj.onc.1210503
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867