Role of somatostatin receptor 1 and 5 on epidermal growth factor receptor mediated signaling

Geetanjali Kharmate1, Padmesh S Rajput, Heather L Watt

  • 1Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada V6T1Z3.

Insights

Somatostatin receptors (SSTRs) inhibit epidermal growth factor (EGF) signaling by blocking EGFR phosphorylation and promoting ErbB complex dissociation. This suggests SSTR activation and EGFR blockade as a potential cancer therapy.

Area of Science:

  • Cellular biology
  • Molecular oncology
  • Signal transduction

Background:

  • Epidermal growth factor (EGF) signaling through its receptor (EGFR) drives cell proliferation in normal and cancerous tissues.
  • Somatostatin (SST) inhibits cell proliferation and is a target for cancer treatment.
  • The interplay between somatostatin receptors (SSTRs) and EGFR signaling is not fully understood.

Purpose of the Study:

  • To investigate the role of SSTR1 and SSTR1/5 in modulating EGF-mediated signaling pathways.
  • To elucidate the effect of SSTRs on EGFR phosphorylation, downstream kinases, and receptor complex formation.

Main Methods:

  • Transfection of human embryonic kidney (HEK) 293 cells with SSTR1 or SSTR1/5.
  • EGFR knockdown using siRNA and treatment with EGFR antagonist AG1478.
  • Analysis of EGFR phosphorylation, MAPK and PI3K/AKT pathway activation.
  • Investigation of EGFR/ErbB2 heteromeric complex formation and dissociation.

Main Results:

  • SSTR1 and SSTR1/5 expression inhibited EGF-induced EGFR phosphorylation, MAPK, and PI3K/AKT signaling.
  • SSTR-mediated inhibition was enhanced by EGFR knockdown or antagonist treatment.
  • SSTRs induced the dissociation of constitutive and EGF-induced EGFR/ErbB2 heteromeric complexes.
  • SSTR1/5 exhibited a more pronounced effect than SSTR1 alone.

Conclusions:

  • SSTRs control EGF-mediated cell survival pathways by dissociating ErbB heteromeric complexes.
  • The combination of SSTR activation and EGFR blockade presents a potential therapeutic strategy for inhibiting tumor proliferation.

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