DNA double-strand break signalling: X-ray energy dependence of residual co-localised foci of gamma-H2AX and 53BP1

Int J Radiat Biol. 2009 Nov;85(11):1042-50. doi: 10.3109/09553000903232884.

Abstract

Purpose: The application of ionising radiation for medical purposes requires the investigation of induced and persistent DNA damages, especially for soft X-rays that are assumed to be more effective than higher energy photons. Therefore, we examined the energy dependent time and dose response of residual DNA damage foci for soft X-rays in comparison to 200 kV photons.

Materials and methods: DNA damage present in cell line 184A1 within 48 h after irradiations with 10 kV, 25 kV and 200 kV photons was analysed by immunochemical detection of co-localised gamma-H2AX (phosphorylated histone H2AX) and 53BP1 (tumour protein 53 binding protein) foci.

Results: The dose dependencies of the colocated foci revealed significant energy dependent differences with increasing amounts of residual foci at decreasing X-ray energy independent on postirradiation time. Dose-dependent RBE (relative biological effectiveness) values ranging from 4 to 7 were determined for 10 kV relative to 200 kV X-rays based on the 24 hour dose responses. For 25 kV photons, ratios considerably higher than one were obtained only for doses above 2 Gy.

Conclusions: The expected energy dependence with increasing DNA damage at decreasing photon energy was confirmed for the residual co-localised foci measured at different time points after irradiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Breast / cytology
  • Breast / metabolism
  • Breast / radiation effects
  • Cell Line
  • DNA Breaks, Double-Stranded*
  • Dose-Response Relationship, Radiation
  • Epithelial Cells / metabolism
  • Epithelial Cells / radiation effects
  • Female
  • Histones / metabolism*
  • Histones / radiation effects*
  • Humans
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Intracellular Signaling Peptides and Proteins / radiation effects*
  • Kinetics
  • Microscopy, Fluorescence
  • Photons / adverse effects
  • Signal Transduction / radiation effects
  • Tumor Suppressor p53-Binding Protein 1

Substances

  • H2AX protein, human
  • Histones
  • Intracellular Signaling Peptides and Proteins
  • TP53BP1 protein, human
  • Tumor Suppressor p53-Binding Protein 1