首页> 美国卫生研究院文献>British Journal of Cancer >Radiation-induced DNA double-strand break rejoining in human tumour cells.
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Radiation-induced DNA double-strand break rejoining in human tumour cells.

机译:辐射诱导的DNA双链断裂在人类肿瘤细胞中重新结合。

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摘要

Five established human breast cancer cell lines and one established human bladder cancer cell line of varying radiosensitivity have been used to determine whether the rejoining of DNA double-strand breaks (dsbs) shows a correlation with radiosensitivity. The kinetics of dsb rejoining was biphasic and both components proceeded exponentially with time. The half-time (t1/2) of rejoining ranged from 18.0 +/- 1.4 to 36.4 +/- 3.2 min (fast rejoining process) and from 1.5 +/- 0.2 to 5.1 +/- 0.2 h (slow rejoining process). We found a statistically significant relationship between the survival fraction at 2 Gy (SF2) and the t1/2 of the fast rejoining component (r = 0.949, P = 0.0039). Our results suggest that cell lines which show rapid rejoining are more radioresistant. These results support the view that, as well as the level of damage induction that we have reported previously, the repair process is a major determinant of cellular radiosensitivity. It is possible that the differences found in DNA dsb rejoining and the differences in DNA dsb induction are related by a common mechanism, e.g. conformation of chromatin in the cell.
机译:已经使用了五种已建立的人类乳腺癌细胞系和一条已建立的具有不同放射敏感性的人类膀胱癌细胞系来确定DNA双链断裂(dsbs)的重新结合是否与放射敏感性相关。 dsb重新结合的动力学是双相的,两个组分随时间呈指数增长。重新加入的半时间(t1 / 2)为18.0 +/- 1.4至36.4 +/- 3.2分钟(快速重新加入过程)和1.5 +/- 0.2至5.1 +/- 0.2 h(缓慢重新加入过程)。我们发现2 Gy的生存分数(SF2)与快速重新结合成分的t1 / 2之间存在统计学上的显着关系(r = 0.949,P = 0.0039)。我们的结果表明显示快速重新结合的细胞系具有更高的抗辐射性。这些结果支持这样一种观点,即,以及我们先前已经报道的损伤诱导水平,修复过程是细胞放射敏感性的主要决定因素。 DNA dsb重新连接中发现的差异与DNA dsb诱导中的差异可能是通过共同的机制(例如细胞中染色质的构象。

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