Oncogenic cooperation between SOCS family proteins and EGFR identified using a Drosophila epithelial transformation model

Héctor Herranz, Xin Hong, Thanh Hung Nguyen, P Mathijs Voorhoeve, Stephen M Cohen

55 Citations (Scopus)

Abstract

MicroRNAs (miRNAs) are emerging as cooperating factors that promote the activity of oncogenes in tumor formation and disease progression. This poses the challenge of identifying the miRNA targets responsible for these interactions. In this study, we identify the growth regulatory miRNA bantam and its target, Socs36E, as cooperating factors in EGFR-driven tumorigenesis and metastasis in a Drosophila model of epithelial transformation. bantam promotes growth by limiting expression of Socs36E, which functions as a negative growth regulator. Socs36E has only a modest effect on growth on its own, but behaves as a tumor suppressor in combination with EGFR activation. The human ortholog of SOCS36E, SOCS5, behaves as a candidate tumor suppressor in cellular transformation in cooperation with EGFR/RAS pathway activation.

Original languageEnglish
JournalGenes & Development
Volume26
Issue number14
Pages (from-to)1602-11
Number of pages10
ISSN0890-9369
DOIs
Publication statusPublished - 15 Jul 2012
Externally publishedYes

Keywords

  • Animals
  • Cell Transformation, Neoplastic
  • Disease Models, Animal
  • Drosophila Proteins
  • Drosophila melanogaster
  • Epithelial Cells
  • Humans
  • MicroRNAs
  • Receptor, Epidermal Growth Factor
  • Receptors, Invertebrate Peptide
  • Suppressor of Cytokine Signaling Proteins
  • Tumor Suppressor Proteins
  • ras Proteins

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