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辐射修饰剂对细胞DNA中X射线诱导损伤比例的影响:用于致死性损伤的测定。

Effect of radiomodifying agents on the ratios of X-ray-induced lesions in cellular DNA: use in lethal lesion determination.

作者信息

Radford I R

出版信息

Int J Radiat Biol Relat Stud Phys Chem Med. 1986 Apr;49(4):621-37. doi: 10.1080/09553008514552871.

Abstract

The effect of three radiomodifying agents, cysteamine, hyperthermia, and hypoxia, on the induction of the major classes of X-ray-induced DNA lesions, was studied using mouse L cells and Chinese hamster V79 cells. The use of filter elution techniques allowed most of these studies to be conducted at X-ray doses within the survival-curve range. Cysteamine was found to protect against DNA single-strand breakage (ssb), DNA base damage, and DNA-protein crosslinkage. Hyperthermia had no effect on the level of DNA ssb or DNA base damage, but in L cells (but not in V79 cells) it increased the level of DNA-protein crosslinkage relative to DNA ssb. Hypoxia protected against DNA ssb, had no significant effect on the level of DNA base damage, and enhanced the level of DNA-protein crosslinkage relative to DNA ssb. These results support the previous suggestion that the X-ray-induced lethal lesion is DNA double-strand breakage. Implications of these findings for the mechanisms of formation of X-ray-induced DNA lesions are also discussed.

摘要

利用小鼠L细胞和中国仓鼠V79细胞,研究了三种辐射修饰剂——半胱胺、热疗和缺氧,对X射线诱导的主要类型DNA损伤的诱导作用。采用滤膜洗脱技术,使得这些研究大多能在存活曲线范围内的X射线剂量下进行。研究发现,半胱胺可防止DNA单链断裂(ssb)、DNA碱基损伤和DNA - 蛋白质交联。热疗对DNA单链断裂或DNA碱基损伤水平没有影响,但在L细胞中(V79细胞中未出现此情况),相对于DNA单链断裂,它会增加DNA - 蛋白质交联水平。缺氧可防止DNA单链断裂,对DNA碱基损伤水平无显著影响,相对于DNA单链断裂,它会提高DNA - 蛋白质交联水平。这些结果支持了之前的观点,即X射线诱导的致死性损伤是DNA双链断裂。本文还讨论了这些发现对X射线诱导DNA损伤形成机制的意义。

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