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DNA Damage Induced in Glioblastoma Cells by 1-131: A Comparison between Experimental Data and Monte Carlo Simulation

机译:胶质母细胞瘤细胞中诱导的DNA损伤1-131:实验数据与蒙特卡罗模拟之间的比较

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The passage of ionizing radiation in living cells creates clusters of damaged nucleotides in DNA. In this study, DNA strand breaks induced by the beta particle of iodine-131 (1-131), have been determined experimentally and compared to Monte Carlo simulation results as a theoretical method of determining131]! damage. For conducting this experimental study, Glioblastoma (GBM) cells were exposed to 10 mCi 1-131, at a dose of 2 Gy, in order create single strand breaks (SSB) and double strand breaks (DSB) in the DNA of irradiated cells. Cells were evaluated quantitatively by the Fast Micromethod assay. The energy spectrum of electrons released in cells were obtained by the macroscopic Monte Carlo code (MCNP4c) and used as an input of the micro Monte Carlo code (MCDS). The percent of damage induced in cells was calculated by Man vitny test. A significant reduction (p<0.05) in fluorescence intensity in irradiated cells compared to control cells as determined by the Fast Micro method assay represented induced SSB and DSB damages in the DNA of irradiated cells. By comparing the experimental and theoretical results, the difference between the percent of SSB per Gy was about 7.4% and DSB was about 1% per Gy. The differences in experimental and theoretical results may be due to the algorithm of applied codes. Since the Fast Micromethod and other experimental techniques do not provide information about the amount of detailed and complex damages of DNA-like base damages, the applied Monte Carlo codes, due to their capability to predict the amount of detailed damages that occur in the DNA of irradiated cells, can be used in in vitro experiments and radiation protection areas.
机译:在活细胞中的电离辐射的通过创建在DNA损伤核苷酸的簇。在这项研究中,DNA链通过碘-131(I-131)的β粒子引起的断裂,已被实验确定,并与蒙特卡罗模拟结果determining131]的理论方法!损害。进行该实验研究,成胶质细胞瘤(GBM)细胞暴露于10毫居里I-131,剂量2Gy的,为了创建单链断裂(SSB),并在辐照细胞的DNA双链断裂(DSB)。细胞通过快速微量法测定定量评价。由宏观蒙特卡洛代码(MCNP4c)获得在细胞中释放电子的能量光谱和用作微蒙特卡洛代码(MCDS)的输入。在细胞损伤的百分比是由曼vitny检验计算。甲显著减少(p <0.05)的荧光强度在照射细胞相比,通过快速微法测定确定控制单元表示在照射细胞的DNA诱导的SSB和DSB损伤。通过比较实验和理论结果,每戈瑞SSB的百分比之间的差值为约7.4%和DSB约为每戈瑞1%。在实验和理论的结果的差异可能是由于所施加的代码的算法。由于快速微量法和其他实验技术不由于其预测详述损害发生在的DNA的量的能力提供有关的DNA样基损害,所施加的蒙特卡罗程序,详细和复杂的损害的量的信息照射细胞,可以在体外实验和辐射防护领域中使用。

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