Activated protease receptor-2 induces GATA6 expression to promote survival in irradiated colon cancer cells

Arch Biochem Biophys. 2014 Aug:555-556:28-32. doi: 10.1016/j.abb.2014.05.021. Epub 2014 Jun 2.

Abstract

Background and aims: The resistance to irradiation is common and a great drawback in the treatment of cancer with radiotherapy; the underlying mechanism is unclear. GATA binding protein 6 (GATA6) is associated with the pathogenesis of cancer. This study aims to investigate the role of GATA6 on compromising irradiation effect on HT55 and HT29 cells, 2 colorectal cancer cell lines.

Methods: Human colon cancer cell lines, HT55 and HT29 cells, were treated with irradiation in the culture. Apoptosis of HT55 and HT29 cells was determined by flow cytometry. The expression of PAR2 and GATA6 in HT55 and HT29 cells was analyzed by real time RT-PCR and Western blotting. The gene silence and gene over expression were employed to observe the effect of GATA6 on p53 expression in HT55 and HT29 cells.

Results: The results showed that HT55 and HT29 cells expressed protease-activated receptor-2 (PAR2). Irradiation induced 38.6% HT55 cell and 33.8% HT29 cell apoptosis, which reduced to 4.2% and 5.6%, respectively after activation of PAR2. Exposure to irradiation increased the expression of GATA6; the latter played a critical role in suppression of p53 expression in HT55 and HT29 cells. Inhibition of GATA6 significantly increased the effect of irradiation on HT55 and HT29 cells.

Conclusions: Activation of PAR2 compromises the effect of irradiation on inducing colorectal cancer cell apoptosis, which can be prevented by inhibition of GATA6 expression.

Keywords: Apoptosis; Colorectal cancer; GATA binding protein 6; Irradiation; Protease-activated receptor-2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / radiation effects
  • Cell Line, Tumor / radiation effects
  • Cell Survival / radiation effects*
  • Colonic Neoplasms
  • GATA6 Transcription Factor / biosynthesis*
  • GATA6 Transcription Factor / genetics
  • Gene Knockdown Techniques
  • Humans
  • Radiation Tolerance*
  • Receptor, PAR-2 / metabolism*
  • Tryptases / metabolism

Substances

  • GATA6 Transcription Factor
  • GATA6 protein, human
  • Receptor, PAR-2
  • Tryptases