Dikomey E
Int J Radiat Biol Relat Stud Phys Chem Med. 1982 Jun;41(6):603-14. doi: 10.1080/09553008214550701.
The effect of hyperthermia on DNA strand break repair was studied in CHO cells. DNA strand breaks were analysed by the alkaline DNA-unwinding technique followed by chromatography on hydroxyapatite. Immediately after irradiation with doses ranging from 2 to 7 Gy, cells were exposed to 42 or 45 degrees C. Heat alone was found to induce DNA strand breaks only at temperatures exceeding 45 degrees C. In comparison to 37 degrees, C, the rate of single-strand break repair was increased by hyperthermia at 42 degrees C, but decreased at 45 degrees C. In contrast hyperthermia at either temperature resulted in a higher number of remaining double-strand breaks 1 hour after irradiation. For the three treatments applied, i.e. X-rays alone or combined with hyperthermia at 42 or 45 degrees C, the relation between cell survival and the number of double-strand breaks measured 1 hour after irradiation could be described by the same function.
在CHO细胞中研究了热疗对DNA链断裂修复的影响。采用碱性DNA解旋技术分析DNA链断裂,随后在羟基磷灰石上进行色谱分析。在用2至7 Gy的剂量照射后,细胞立即暴露于42或45摄氏度。发现仅在温度超过45摄氏度时,热疗本身会诱导DNA链断裂。与37摄氏度相比,42摄氏度的热疗可提高单链断裂修复率,但在45摄氏度时则降低。相反,在任一温度下的热疗在照射后1小时都会导致更多的双链断裂残留。对于所应用的三种处理,即单独的X射线或与42或45摄氏度的热疗联合应用,照射后1小时测得的细胞存活率与双链断裂数量之间的关系可用相同的函数来描述。