AT Cells Show Dissimilar Hypersensitivity to Heavy-Ion and X-rays Irradiation
Author(s) -
Shoichiro Kitajima,
Hideaki Nakamura,
Makoto Adachi,
Kei Ijichi,
Yoshihiro Yasui,
Noriko Saito,
Masao Suzuki,
Kenichi Kurita,
Kanji Ishizaki
Publication year - 2010
Publication title -
journal of radiation research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.643
H-Index - 60
eISSN - 1349-9157
pISSN - 0449-3060
DOI - 10.1269/jrr.09069
Subject(s) - irradiation , linear energy transfer , ataxia telangiectasia , relative biological effectiveness , ion , radiochemistry , radiation sensitivity , non homologous end joining , heavy ion , proton , gamma ray , chemistry , dna damage , dna , physics , biochemistry , nuclear physics , organic chemistry
Ataxia telangiectasia (AT) cells, with their defective double-strand break (DSB) repair processes, exhibit high sensitivity to low-LET radiation such as X-rays irradiation and gamma beams. Since heavy ion beam treatment for cancer is becoming increasingly common in Japan and elsewhere, it is important to also determine their sensitivity to high-LET radiation. For this purpose we irradiated AT and normal human cells immortalized with the human telomerase gene using high- (24-60 keV/microm carbon and 200 keV/microm iron ions) or low-LET (X-rays) radiation in non-proliferative conditions. In normal cells the RBE (relative biological effectiveness) of carbon and iron ions increased from 1.19 to 1.81 in proportion to LET. In contrast, their RBE in AT cells increased from 1.32 at 24 keV/microm to 1.59 at 40 keV/microm, and exhibited a plateau at over 40 keV/microm. In normal cells most gamma-H2AX foci induced by both carbon- and iron-ion beams had disappeared at 40 h. In AT cells, however, a significant number of gamma-H2AX foci were still observed at 40 h. The RBEs found in the AT cells after heavy-ion irradiation were consistent with the effects predicted from the presence of non-homologous end joining defects. The DSBs remaining after heavy-ion irradiation suggested defects in the AT cells' DSB repair ability.
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