Jorritsma J B, Burgman P, Kampinga H H, Konings A W
Radiat Res. 1986 Mar;105(3):307-19.
Possible relations between hyperthermic inactivation of alpha and beta DNA polymerase activity and hyperthermic cell killing or hyperthermic radiosensitization were investigated. Ehrlich Ascites Tumor (EAT) cells and HeLa S3 cells were treated with fractionated doses of hyperthermia. The heating schedules were chosen such that the initial heat treatment resulted in either thermotolerance or thermosensitization (step-down heating) for the second heat treatment. The results show that for DNA polymerase activity and heat radiosensitization (cell survival) no thermotolerance or thermosensitization is observed. Thus hyperthermic cell killing and DNA polymerase activity are not correlated. The correlation of hyperthermic radiosensitization and DNA polymerase activity was substantially less than observed in previous experiments with normotolerant and thermotolerant HeLa S3 cells. We conclude that alpha and beta DNA polymerase inactivation is not always the critical cellular process responsible for hyperthermic cell killing or hyperthermic radiosensitization. Other possible cellular systems that might determine these processes are discussed.
研究了α和β DNA聚合酶活性的热失活与热诱导细胞杀伤或热诱导放射增敏之间的可能关系。对艾氏腹水瘤(EAT)细胞和HeLa S3细胞进行了分次热疗。选择加热方案,使初次热处理对第二次热处理产生热耐受或热敏化(逐步降温加热)。结果表明,对于DNA聚合酶活性和热放射增敏(细胞存活),未观察到热耐受或热敏化。因此,热诱导细胞杀伤与DNA聚合酶活性不相关。热诱导放射增敏与DNA聚合酶活性的相关性明显低于先前对正常耐受和热耐受的HeLa S3细胞进行的实验中所观察到的。我们得出结论,α和β DNA聚合酶失活并不总是导致热诱导细胞杀伤或热诱导放射增敏的关键细胞过程。还讨论了其他可能决定这些过程的细胞系统。