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首页> 外文期刊>International Journal of Radiation Biology: Covering the Physical, Chemical, Biological, and Medical Effects of Ionizing and Non-ionizing Radiations >Radiation-induced arrest of cells in G2 phase elicits hypersensitivity to DNA double-strand break inducers and an altered pattern of DNA cleavage upon re-irradiation.
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Radiation-induced arrest of cells in G2 phase elicits hypersensitivity to DNA double-strand break inducers and an altered pattern of DNA cleavage upon re-irradiation.

机译:辐射诱导的G2期细胞停滞引起对DNA双链断裂诱导剂的超敏反应,并在重新辐射后改变了DNA切割的模式。

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PURPOSE: To determine how radiation-induced arrest in G2 affects the response of mammalian cells to a challenging dose of radiation or to antitumour drugs producing DNA double-strand breaks. MATERIALS AND METHODS: V79 fibroblast survival to 5 Gy gamma-rays followed at intervals by 3 Gy irradiation or by contact with an equitoxic dose of neocarzinostatin or etoposide, was measured by clonogenic assays. The pattern of radiation-induced DNA double-strand breaks was determined by filter elution and CFGE (continuous field gel electrophoresis) or PFGE (pulsed-field gel electrophoresis) in G2-arrested cells as well as in nonpre-irradiated asynchronous or synchronized cells. The cell-cycle phase specificity of drug susceptibility was determined in synchronized HeLa cells. RESULTS: Cell kill by radiation-drug combined treatment varied markedly with the time elapsed after priming irradiation. Pre-irradiated, G2-arrested V79 fibroblasts demonstrated excess double-stranded DNA cleavage upon re-irradiation and hypersensitivity to drugs and radiation, although maximum resistance to both neocarzinostatin and etoposide in synchronized HeLa cells was in G2. This effect occurred in the megabase range only, with a peak around 4 Mbp; no change in the electrophoretic migration profile of DNA was observed below 1 Mbp. Moreover, the DNA migration profile and the yield of DNA cleavage in G2-arrested cells were close to those expected from S-phase cells. CONCLUSION: The available data suggest that mechanisms operating within the radiation-induced G2 block promote susceptibility to DNA double-strand break inducers at this stage. It is also proposed that the conformation of DNA in cells accumulated in G2 following irradiation bears resemblance to that for cells in S phase, due either to active repair mechanisms or to inhibition of chromosome disentanglement at the S-G2 transition.
机译:目的:确定辐射诱导的G2阻滞如何影响哺乳动物细胞对具有挑战性的辐射剂量或产生DNA双链断裂的抗肿瘤药物的反应。材料与方法:通过克隆形成测定法测定V79成纤维细胞在5 Gyγ射线下的存活率,然后间隔3 Gy照射或与等毒性剂量的新carzinostatin或依托泊苷接触。辐射诱导的DNA双链断裂的模式是通过在G2阻滞细胞以及未预辐照的异步或同步细胞中通过滤膜洗脱和CFGE(连续场凝胶电泳)或PFGE(脉冲场凝胶电泳)确定的。在同步化的HeLa细胞中确定了药物敏感性的细胞周期阶段特异性。结果:放射-药物联合处理对细胞的杀伤作用与引发辐射后所经过的时间显着不同。预辐照的,G2阻滞的V79成纤维细胞在再次辐照后对药物和放射过敏时显示出过量的双链DNA裂解,尽管在同步化的HeLa细胞中对新carcarinostatin和依托泊苷的最大抗性是在G2中。该效应仅在兆碱基范围内发生,峰值在4 Mbp左右。低于1 Mbp时,未观察到DNA电泳迁移图谱的变化。此外,G2阻滞细胞中的DNA迁移曲线和DNA裂解的产率接近S期细胞的预期。结论:现有数据表明,在此阶段,在辐射诱导的G2阻滞内起作用的机制促进了对DNA双链断裂诱导剂的敏感性。也有人提出,由于主动修复机制或抑制了S-G2转变中染色体解缠结,辐射后G2中积累的细胞中DNA的构象与S期细胞的构象相似。

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