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对两种亚硝基脲化合物与大鼠脑肿瘤细胞中X射线相互作用的分析。

An analysis of the interaction between two nitrosourea compounds and X-radiation in rat brain tumour cells.

作者信息

Leenhouts H P, Chadwick K H, Deen D F

出版信息

Int J Radiat Biol Relat Stud Phys Chem Med. 1980 Feb;37(2):169-81. doi: 10.1080/09553008014550211.

Abstract

Experimental measurements have shown that both BCNU [1,3-bis(2-chloroethyl)-1-nitrosourea] and CCNU [1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea] are toxic in rat 9L brain tumour cells and also sensitize these cells to the action of ionizing radiation. The interaction of BCNU and CCNU with radiation has been interpreted using a recently developed extension of the molecular theory of cell survival. The experimental results are shown to be compatible with the mathematical equations predicted by the model and the analysis indicates that the sensitizing effect is caused by a synergistic interaction between sublethal damage caused by the nitrosourea compound and the radiation at the molecular level. The analysis of the dependence of the interaction on the time between nitrosourea treatment and radiation indicates that the optimal interaction occurs with a 5 hour interval.

摘要

实验测量表明,卡莫司汀[1,3-双(2-氯乙基)-1-亚硝基脲]和洛莫司汀[1-(2-氯乙基)-3-环己基-1-亚硝基脲]对大鼠9L脑肿瘤细胞均具有毒性,并且还能使这些细胞对电离辐射的作用敏感化。使用最近发展的细胞存活分子理论扩展来解释卡莫司汀和洛莫司汀与辐射的相互作用。实验结果表明与该模型预测的数学方程相符,并且分析表明,敏化效应是由亚硝基脲化合物和辐射在分子水平上造成的亚致死损伤之间的协同相互作用引起的。对亚硝基脲处理和辐射之间相互作用对时间的依赖性分析表明,最佳相互作用发生在间隔5小时时。

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