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低剂量辐射下11种细胞系初始DNA损伤以及修复12小时后残留DNA损伤的测定。

Determination of the initial DNA damage and residual DNA damage remaining after 12 hours of repair in eleven cell lines at low doses of irradiation.

作者信息

Roos W P, Binder A, Böhm L

机构信息

Department of Radiation Oncology, Faculty of Medicine, University of Stellenbosch, Tygerberg, South Africa.

出版信息

Int J Radiat Biol. 2000 Nov;76(11):1493-500. doi: 10.1080/09553000050176252.

Abstract

PURPOSE

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.

MATERIALS AND METHODS

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).

RESULTS

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.

CONCLUSION

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.

摘要

目的

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。

材料与方法

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。

结果

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。

结论

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。

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