Radiosensitization of metformin in pancreatic cancer cells via abrogating the G2 checkpoint and inhibiting DNA damage repair

Cancer Lett. 2015 Dec 1;369(1):192-201. doi: 10.1016/j.canlet.2015.08.015. Epub 2015 Aug 21.

Abstract

Recent evidences have demonstrated the potential of metformin as a novel agent for cancer prevention and treatment. Here, we investigated its ability of radiosensitization and the underlying mechanisms in human pancreatic cancer cells. In this study, we found that metformin at 5 mM concentration enhanced the radiosensitivity of MIA PaCa-2 and PANC-1 cells, with sensitization enhancement ratios of 1.39 and 1.27, respectively. Mechanistically, metformin caused abrogation of the G2 checkpoint and increase of mitotic catastrophe, associated with suppression of Wee1 kinase and in turn CDK1 Tyr15 phosphorylation. Furthermore, metformin inhibited both expression and irradiation-induced foci formation of Rad51, a key player in homologous recombination repair, ultimately leading to persistent DNA damage, as reflected by γ-H2AX and 53BP1 signaling. Finally, metformin-mediated AMPK/mTOR/p70S6K was identified as a possible upstream pathway controlling translational regulation of Wee1 and Rad51. Our data suggest that metformin radiosensitizes pancreatic cancer cells in vitro via abrogation of the G2 checkpoint and inhibition of DNA damage repair. However, the in vivo study is needed to further confirm the findings from the in vitro study.

Keywords: Metformin; Pancreatic cancer; Rad51; Radiosensitizer; Wee1; mTOR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / radiation effects
  • CDC2 Protein Kinase
  • Cell Cycle Proteins / antagonists & inhibitors
  • Cell Cycle Proteins / metabolism
  • Cell Line, Tumor
  • Chemoradiotherapy
  • Cyclin-Dependent Kinases / metabolism
  • DNA Damage*
  • DNA Repair*
  • G2 Phase Cell Cycle Checkpoints*
  • Humans
  • Metformin / pharmacology*
  • Mitosis / drug effects
  • Nuclear Proteins / antagonists & inhibitors
  • Nuclear Proteins / metabolism
  • Pancreatic Neoplasms / pathology
  • Pancreatic Neoplasms / therapy*
  • Phosphorylation
  • Protein Biosynthesis / drug effects
  • Protein Processing, Post-Translational / drug effects
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Protein-Tyrosine Kinases / metabolism
  • Rad51 Recombinase / metabolism
  • Radiation Tolerance
  • Radiation-Sensitizing Agents / pharmacology*

Substances

  • Cell Cycle Proteins
  • Nuclear Proteins
  • Radiation-Sensitizing Agents
  • Metformin
  • Protein-Tyrosine Kinases
  • WEE1 protein, human
  • CDC2 Protein Kinase
  • CDK1 protein, human
  • Cyclin-Dependent Kinases
  • RAD51 protein, human
  • Rad51 Recombinase