Effects of RING-SH2Grb², a chimeric protein containing the E3 ligase domain of Cbl, on the EGFR pathway

Chin J Physiol. 2014 Dec 31;57(6):350-7. doi: 10.4077/CJP.2014.BAD281.

Abstract

The E3 ubiquitin-protein ligase Casitas B-lineage lymphoma protein (Cbl) negatively regulates epidermal growth factor receptor (EGFR) signaling pathway in many organisms, and has crucial roles in cell growth, development and human pathologies, including lung cancers. RING-SH2Grb² a chimeric protein of 215 amino acids containing the RING domain of Cbl that provides E3 ligase activity, and the SH2 domain of Grb2 that serves as an adaptor for EGFR. In this study, we demonstrated that RING-SH2Grb² could promote the ubiquitinylation and degradation of EGFR in a human non-small cell lung carcinoma cell line H1299. Moreover, we discovered that the RING-SH2Grb² chimera promoted the internalization of ligand-bound EGFR, inhibited the growth of H1299 cells, and significantly suppressed tumor growth in a xenograft mouse model. In summary, our results revealed a potential new cancer therapeutic approach for non-small cell lung cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • ErbB Receptors / physiology*
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • GRB2 Adaptor Protein / pharmacology*
  • Humans
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Neoplasms, Experimental / drug therapy
  • Proto-Oncogene Proteins c-cbl / pharmacology*
  • Recombinant Fusion Proteins / pharmacology*
  • Signal Transduction / physiology*
  • src Homology Domains

Substances

  • GRB2 Adaptor Protein
  • GRB2 protein, human
  • Recombinant Fusion Proteins
  • Proto-Oncogene Proteins c-cbl
  • ErbB Receptors
  • Extracellular Signal-Regulated MAP Kinases