Cellular inactivation and chromosomal aberrations:: Initial damage

被引:1
|
作者
Boissière, A
Eschenbrenner, A
Gobert, F
du Penhoat, MAH
Abel, F
Lamoureux, M
Martins, L
Politis, MF
Ricoul, M
Touati, A
Sage, E
Sabatier, L
Chetioui, A
机构
[1] Univ Paris 06, CNRS, UMR, Ctr Phys Solides, F-75251 Paris 05, France
[2] Univ Paris 07, CNRS, UMR, Ctr Phys Solides, F-75251 Paris 05, France
[3] Lab Radiobiol & Oncol, Fontenay Aux Roses, France
[4] Inst Curie Rech, Lab Genotox & Modulat Express Gen, Orsay, France
关键词
ionizing radiation; core ionizations; chromosomal aberrations; cell inactivation; ultrasoft X-rays; DNA; initial events;
D O I
10.1615/JEnvPathToxOncol.v23.i2.30
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
It has been proposed that unrepaired or misrepaired complex lesions of DNA are responsible for cell inactivation and chromosomal aberrations. The detailed features of the critical damage and the nature of initiating physical events are actively investigated. We studied the role of inner-shell (core) ionizations in DNA atoms is studied. Ultrasoft X-rays from LURE synchrotron radiation have been used to mimic core events induced by ionizing radiations. For biological matter, inner-shell photoionization is indeed the main interaction channel of these radiations. Moreover, by tuning the X-ray energy below and above the carbon K-threshold, it is possible to achieve a two-fold increase in the number of core-ionizations in DNA for a same dose. Cell survival and chromosome aberrations have thus been studied at three iso-attenuated energies: 250,350, and 810 eV. Relative biological efficiencies (RBEs) for cell inactivation and chromosome aberrations were found to be strongly correlated with the yields of core events in DNA.
引用
收藏
页码:107 / 115
页数:9
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