Roos W P, Binder A, Böhm L
Department of Radiation Oncology, Faculty of Medicine, University of Stellenbosch, Tygerberg, South Africa.
Int J Radiat Biol. 2000 Nov;76(11):1493-500. doi: 10.1080/09553000050176252.
To determine the relationship between DNA damage and radiosensitivity at low doses (1-10 Gy) for the initial DNA damage and residual DNA damage remaining after 12-h repair.
Eleven cell lines, normal human lung epithelial L132, HT29 human colon carcinoma, ATs4 human ataxia telangiectasia, normal CHO-K1 hamster, repair-deficient xrs1 and xrs5 mutants, repair-deficient SCID rodent cell line, the human normal fibroblast 1BR.3, human ataxia telangiectasia fibroblast AT1BR and the repair-deficient fibroblasts 180BR.B and 46BR.1 were irradiated with 60Co gamma-rays. Radiosensitivity was measured by clonogenic survival assay. DNA damage was measured by fluorometric analysis of DNA unwinding (FADU).
The radiosensitivity in the 11 cell lines ranged from SF2 of 0.02-0.61. By FADU assay, the undamaged DNA at 5-Gy ranged from 56 to 93%. The initial DNA damage and radiosensitivity were highly correlated (r2 = 0.81). After 5-Gy irradiation and 12-h repair, two groups of cell lines emerged. Group 1 restored undamaged DNA to a level ranging from 94 to 98%. Group 2 restored the undamaged DNA to a level ranging from 77 to 82%. No correlation was seen between residual DNA damage remaining after 12-h repair and radiosensitivity.
It is shown that the initial DNA damage correlates with radiosensitivity at low doses of irradiation. This suggests that the initial DNA damage must be considered as a determinant for radiosensitivity.
确定低剂量(1 - 10 Gy)照射时初始DNA损伤与12小时修复后残留DNA损伤之间的关系以及它们与放射敏感性的关系。
用60Coγ射线照射11种细胞系,包括正常人肺上皮L132细胞系、HT29人结肠癌细胞系、ATs4人共济失调毛细血管扩张症细胞系、正常CHO - K1仓鼠细胞系、修复缺陷型xrs1和xrs5突变体细胞系、修复缺陷型SCID啮齿动物细胞系、人正常成纤维细胞1BR.3、人共济失调毛细血管扩张症成纤维细胞AT1BR以及修复缺陷型成纤维细胞180BR.B和46BR.1。通过克隆形成存活试验测量放射敏感性,通过DNA解旋荧光分析(FADU)测量DNA损伤。
11种细胞系的放射敏感性范围为SF2为0.02 - 0.61。通过FADU试验,5 Gy照射时未损伤的DNA范围为56%至93%。初始DNA损伤与放射敏感性高度相关(r2 = 0.81)。5 Gy照射并修复12小时后,出现了两组细胞系。第1组将未损伤的DNA恢复到94%至98%的水平。第2组将未损伤的DNA恢复到77%至82%的水平。12小时修复后残留的DNA损伤与放射敏感性之间没有相关性。
结果表明,低剂量照射时初始DNA损伤与放射敏感性相关。这表明初始DNA损伤必须被视为放射敏感性的一个决定因素。