RNAi silencing targeting RNF8 enhances radiosensitivity of a non-small cell lung cancer cell line A549

Int J Radiat Biol. 2013 Sep;89(9):708-15. doi: 10.3109/09553002.2013.792964. Epub 2013 May 15.

Abstract

Purpose: The E3 ubiquitin ligase RNF8 regulates the accumulation or removal of a number of proteins at DNA lesions, thereby playing a critically important role in DNA damage response. The present study investigated the possibility of using RNF8 as a new target in the radiation treatment of human non-small cell lung cancer.

Methods and materials: We used RNA interference technology to silence the expression of RNF8 in A549 cells, and then detected the radiation response by colony forming assays. DNA repair was monitored by γ-H2AX foci formation after RNF8 depletion. Expression of Ku70 and Rad51 were assessed by immunofluorescent staining and Western blotting. Cell cycle and apoptosis were measured by flow cytometry assays.

Results: After lentivirus-mediated siRNA transfection, expression of RNF8 in A549 cells downregulated which led to an increased radiosensitivity and impaired DNA repair. RNF8 knockdown did not affect Ku70 expression, however, Rad51, a key player in homologous recombination (HR) repair, was abrogated at sites of DNA damage. Furthermore, we observed an extended G2/M arrest and an increased induction of apoptosis after ionizing radiation in the absence of RNF8.

Conclusions: RNF8 silencing effectively downregulates Rad51 therefore maybe impairing HR repair, and prolongs the G2/M accumulation as well as cell apoptosis upon radiation, which all suggest an enhanced radiosensitivity on A549 cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / radiation effects
  • Carcinoma, Non-Small-Cell Lung / radiotherapy*
  • Cell Cycle / radiation effects
  • Cell Line, Tumor
  • DNA Breaks, Double-Stranded
  • DNA-Binding Proteins / antagonists & inhibitors*
  • DNA-Binding Proteins / genetics
  • Down-Regulation
  • Histones / analysis
  • Humans
  • Lentivirus / genetics
  • Lung Neoplasms / radiotherapy*
  • RNA Interference*
  • Rad51 Recombinase / genetics
  • Radiation Tolerance*
  • Ubiquitin-Protein Ligases

Substances

  • DNA-Binding Proteins
  • H2AX protein, human
  • Histones
  • RNF8 protein, human
  • Ubiquitin-Protein Ligases
  • Rad51 Recombinase