Profilin1 sensitizes pancreatic cancer cells to irradiation by inducing apoptosis and reducing autophagy

Curr Mol Med. 2013 Sep;13(8):1368-75. doi: 10.2174/15665240113139990060.

Abstract

Pancreatic cancer has an extremely poor prognosis mainly due to lack of effective treatment options. Radiotherapy is mostly applied to locally advanced cases, although tumor radioresistance limits the effectiveness. Profilin1, a novel tumor suppressor gene, was reported to be down-regulated in various cancers and associated with tumor progression. The objective of this study was to demonstrate how profilin1 affected pancreatic cancer radiosensitivity. We showed profilin1 was down-regulated in pancreatic cancer cells after exposure to radiation, and re-expression of profilin1 suppressed tumor cell viability and increased DNA damage following irradiation. Further studies revealed that up-regulation of profilin1 facilitated apoptosis and repressed autophagy induced by irradiation, which might sensitize pancreatic cancer cells to radiation treatment. Our findings may provide a novel therapeutic strategy for sensitizing pancreatic cancer to radiotherapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / genetics*
  • Apoptosis / radiation effects*
  • Autophagy / genetics
  • Autophagy / radiation effects
  • Cell Line
  • DNA Damage / radiation effects
  • Gene Expression Regulation, Neoplastic / radiation effects
  • Humans
  • Mice
  • Pancreatic Neoplasms / genetics*
  • Pancreatic Neoplasms / pathology
  • Profilins / genetics*
  • Radiation Tolerance / genetics*
  • X-Rays / adverse effects
  • Xenograft Model Antitumor Assays

Substances

  • Profilins