G2-chromosome aberrations induced by high-LET radiations

Adv Space Res. 2001;27(2):383-91. doi: 10.1016/s0273-1177(01)00006-0.

Abstract

We report measurement of initial G2-chromatid breaks in normal human fibroblasts exposed to various types of high-LET particles. Exponentially growing AG 1522 cells were exposed to gamma rays or heavy ions. Chromosomes were prematurely condensed by calyculin A. Chromatid-type breaks and isochromatid-type breaks were scored separately. The dose response curves for the induction of total chromatid breaks (chromatid-type + isochromatid-type) and chromatid-type breaks were linear for each type of radiation. However, dose response curves for the induction of isochromatid-type breaks were linear for high-LET radiations and linear-quadratic for gamma rays. Relative biological effectiveness (RBE), calculated from total breaks, showed a LET dependent tendency with a peak at 55 keV/micrometer silicon (2.7) or 80 keV/micrometer carbon (2.7) and then decreased with LET (1.5 at 440 keV/micrometer). RBE for chromatid-type break peaked at 55 keV/micrometer (2.4) then decreased rapidly with LET. The RBE of 440 keV/micrometer iron particles was 0.7. The RBE calculated from induction of isochromatid-type breaks was much higher for high-LET radiations. It is concluded that the increased production of isochromatid-type breaks, induced by the densely ionizing track structure, is a signature of high-LET radiation exposure.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Cell Line
  • Cells, Cultured
  • Chromatids / radiation effects
  • Chromosome Aberrations*
  • Chromosomes / drug effects
  • DNA Damage
  • Dose-Response Relationship, Radiation
  • Enzyme Inhibitors / pharmacology
  • Fibroblasts / radiation effects
  • G2 Phase / radiation effects*
  • Gamma Rays*
  • Heavy Ions*
  • Humans
  • Linear Energy Transfer
  • Marine Toxins
  • Oxazoles / pharmacology
  • Phosphoprotein Phosphatases / antagonists & inhibitors
  • Relative Biological Effectiveness

Substances

  • Enzyme Inhibitors
  • Marine Toxins
  • Oxazoles
  • calyculin A
  • Phosphoprotein Phosphatases