Double-strand breaks on F98 glioma rat cells induced by minibeam and broad-beam synchrotron radiation therapy

Clin Transl Oncol. 2014 Aug;16(8):696-701. doi: 10.1007/s12094-013-1134-x. Epub 2013 Nov 23.

Abstract

Purpose: To assess the DNA damage induced by MBRT and BB radiations on glioma cells.

Methods: The analysis of fluorescent intensity emitted per nucleus was plotted versus DNA content 2 and 17 h after irradiations. At around cell-doubling time (17 h) after exposures, the remaining DNA radiation damage could be correlated with cellular death.

Results: A higher γH2AX IF intensity per cell could be detected 2 and 17 h after MBRT when compared with BB. 17 h after MBRT, misrepaired damaged cells remained arrested in both G1 and G2 phases.

Conclusions: A pronounced G2 phase arrest was detected at 17 h after MBRT and BB. However, only after MBRT, a dose-dependent increasing number of damaged cells appeared arrested also in the G1 phase, and a higher amount of cells more prone to undergo apoptosis were detected. The threshold dose required to enhance the effectiveness of both synchrotron radiation techniques was 12 Gy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • DNA Breaks, Double-Stranded / radiation effects*
  • Glioma / genetics*
  • Radiotherapy / methods*
  • Rats
  • Synchrotrons