Phenformin alone or combined with gefitinib inhibits bladder cancer via AMPK and EGFR pathways

Cancer Commun (Lond). 2018 Jul 27;38(1):50. doi: 10.1186/s40880-018-0319-7.

Abstract

Background: In previous studies, we have shown that the combination of metformin and gefitinib inhibits the growth of bladder cancer cells. Here we examined whether the metformin analogue phenformin, either used alone or in combination with gefitinib, could inhibit growth of bladder cancer cells.

Methods: The growth-inhibitory effects of phenformin and gefitinib were tested in one murine and two human bladder cancer cell lines using MTT and clonogenic assays. Effects on cell migration were assessed in a wound healing assay. Synergistic action between the two drugs was assessed using CompuSyn software. The potential involvement of AMPK and EGFR pathways in the effects of phenformin and gefitinib was explored using Western blotting.

Results: In MTT and clonogenic assays, phenformin was > 10-fold more potent than metformin in inhibiting bladder cancer cell growth. Phenformin also potently inhibited cell migration in wound healing assays, and promoted apoptosis. AMPK signaling was activated; EGFR signaling was inhibited. Phenformin was synergistic with gefitinib, with the combination of drugs showing much stronger anticancer activity and apoptotic activation than phenformin alone.

Conclusions: Phenformin shows potential as an effective drug against bladder cancer, either alone or in combination with gefitinib.

Keywords: AMPK; Bladder cancer; EGFR; Gefitinib; Phenformin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases / metabolism*
  • Animals
  • Apoptosis / drug effects
  • Cell Line, Tumor
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Drug Synergism
  • ErbB Receptors / metabolism*
  • Gefitinib / pharmacology*
  • Humans
  • Inhibitory Concentration 50
  • Mice
  • Phenformin / pharmacology*
  • Signal Transduction / drug effects
  • Urinary Bladder Neoplasms / metabolism
  • Urinary Bladder Neoplasms / pathology

Substances

  • Phenformin
  • ErbB Receptors
  • AMP-Activated Protein Kinases
  • Gefitinib