Radiation induced DNA damage and damage repair in three human tumour cell lines

Mutat Res. 1996 Jan 2;362(1):51-9. doi: 10.1016/0921-8777(95)00032-1.

Abstract

Three human tumour cell lines (HX142, RT112 and MGH-U1) with different radiosensitivities were tested for differences in the rate and/or extent of DNA unwinding in alkali as well as for differences in the induction of DNA double strand breaks by means of the pulsed field gel electrophoresis, after X-irradiation. Unlike that which has been found using the non-denaturing filter elution technique (NDE, McMillan et al., 1990), no differences in initial DNA damage (the extent of alkaline unwinding and the induction of double strand breaks) were found for the three cell lines. These data suggest that rather than a different number of DNA lesions per Da per Gy between these cell lines, structural differences in chromatin structure (related to radiosensitivity) might impair the detectability of lesions in some assays like the NDE. The nature of such structure differences remains unclear. However, the differences did not affect alkaline unwinding profiles, as all three cell lines showed identical rates of DNA unwinding after exposure to X-rays. Furthermore, the three cell lines did not show significant differences in the kinetics of DNA strand break rejoining nor in the amounts of damage remaining after 24 h repair. The results obtained in this study, together with other findings, suggest that the three cell lines may differ in their 'presentation' of DNA damage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Survival / radiation effects
  • Chromatin / chemistry
  • DNA Damage / physiology*
  • DNA Repair*
  • DNA, Neoplasm / radiation effects*
  • Electrophoresis, Gel, Pulsed-Field
  • Genetic Techniques
  • Humans
  • Hydrogen-Ion Concentration
  • Kinetics
  • Neuroblastoma
  • Nucleic Acid Denaturation
  • Radiation Tolerance / physiology*
  • Sodium Hydroxide
  • Tumor Cells, Cultured / radiation effects
  • Urinary Bladder Neoplasms

Substances

  • Chromatin
  • DNA, Neoplasm
  • Sodium Hydroxide