| Literature DB >> 34019659 |
Igor Shuryak1, Bradford D Loucas2, Michael N Cornforth2.
Abstract
The large majority of chromosome damage produced by ionizing radiations takes the form of exchange aberrations. For simple exchanges between two chromosomes, multi-fluor fluorescence in situ hybridization (mFISH) studies confirm that the dose response to X rays or gamma rays is quasilinear with dose. This result is in seeming conflict with generalized theories of radiation action that depend on the interaction of lesions as the source of curvature in dose-response relationships. A qualitative explanation for such "linearization" had been previously proposed but lacked quantitative support. The essence of this explanation is that during the rejoining of radiogenic chromosome breaks, competition for breaks (CFB) between different aberration types often results in formation of complex exchange aberrations at the expense of simple reciprocal exchange events. This process becomes more likely at high radiation doses, where the number of contemporaneous breaks is high and complex exchanges involving multiple breaks become possible. Here we provide mathematical support for this CFB concept under the assumption that the mean and variance for exchange complexity increase with radiation dose. ©2021 by Radiation Research Society. All rights of reproduction in any form reserved.Entities:
Mesh:
Year: 2021 PMID: 34019659 PMCID: PMC8440481 DOI: 10.1667/RADE-20-00253.1
Source DB: PubMed Journal: Radiat Res ISSN: 0033-7587 Impact factor: 3.372