Enhanced degradation of epidermal growth factor receptor by metformin

  • Mayuka Yamagata
    Division of Oral and Maxillofacial Surgery, Department of Science of Physical Functions Kyushu Dental University Kitakyushu Japan
  • Sen Higashi
    Division of Applied Pharmacology, Department of Health Promotion Kyushu Dental University Kitakyushu Japan
  • Noboru Yaida
    Division of Oral and Maxillofacial Surgery, Department of Science of Physical Functions Kyushu Dental University Kitakyushu Japan
  • Akane Ichihara
    Division of Applied Pharmacology, Department of Health Promotion Kyushu Dental University Kitakyushu Japan
  • Manabu Habu
    Division of Oral and Maxillofacial Surgery, Department of Science of Physical Functions Kyushu Dental University Kitakyushu Japan
  • Masaaki Sasaguri
    Division of Oral and Maxillofacial Surgery, Department of Science of Physical Functions Kyushu Dental University Kitakyushu Japan
  • Kazuhiro Tominaga
    Division of Oral and Maxillofacial Surgery, Department of Science of Physical Functions Kyushu Dental University Kitakyushu Japan
  • Hiroshi Takeuchi
    Division of Applied Pharmacology, Department of Health Promotion Kyushu Dental University Kitakyushu Japan

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<jats:title>Abstract</jats:title><jats:sec><jats:title>Aim</jats:title><jats:p>Epidermal growth factor receptor (EGFR) is one of the most extensively studied molecular targets for newly developed antitumor drugs. Metformin, a widely used antidiabetic drug for type 2 diabetes, is expected to exhibit antitumor activity. Recently, it was reported that EGFR expression in tumor tissues from patients with type 2 diabetes was reduced in patients taking metformin compared with that in patients not taking metformin. Therefore, we investigated the effect of metformin on the expression of EGFR at the cellular level.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>Cell lines derived from oral squamous cell carcinoma were used to investigate the effect of metformin on the cell proliferation and cellular content of EGFR. Cell proliferation was assessed by direct cell counting and water‐soluble tetrazolium (WST)‐based colorimetric assay. Expression level of EGFR messenger ribonucleic acid (mRNA) and protein were analyzed by real‐time polymerase chain reaction (PCR) and western blotting, respectively.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>The proliferation of all three cell lines used in this study (Ca9‐22, SAS, and HSC‐2) was suppressed by metformin. Metformin downregulated the cellular content of EGFR without affecting its mRNA expression. Ligand‐induced EGFR internalization was accelerated by metformin. Ligand‐induced EGFR degradation was inhibited by the lysosomal and proteasomal inhibitors bafilomycin A1 and MG132, respectively.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>These results suggest that metformin reduces EGFR by modifying the intracellular trafficking of the receptor, for example, promoting ligand‐induced internalization and degradation of EGFR, rather than suppressing the synthesis of the receptor. The effect of metformin on EGFR may affect therapeutic outcomes when metformin is combined with existing cancer treatments.</jats:p></jats:sec>

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