Iliakis G, Seaner R, Okayasu R
Thomas Jefferson University, Department of Radiation Oncology, Philadelphia, PA.
Int J Hyperthermia. 1990 Jul-Aug;6(4):813-33. doi: 10.3109/02656739009140828.
The effect of heat on the induction and repair of DNA single (ssb) and double (dsb) strand breaks was studied in irradiated exponentially growing or plateau-phase CHO cells and their DNA dsb repair-deficient, radiation-sensitive counterpart, the xrs-5 cells. Induction and repair of DNA ssb was measured by the alkaline unwinding technique, whereas induction and repair of DNA dsb was measured by the non-unwinding filter elution technique. The results indicated that pre-exposure of cells to heat (45 x 5 degrees C) for 8-30 min did not affect the induction of DNA ssb or DNA dsb per Gy and dalton of DNA in CHO or xrs-5 cells, tested either in the exponential or in the plateau-phase of growth. On the other hand, pre-exposure to heat inhibited DNA repair processes and increased the fraction of unrepaired radiation-induced damage measured 2 h after irradiation. Repair of DNA dsb was more heat-sensitive than repair of DNA ssb in both cell lines. Repair of radiation-induced ssb or dsb was inhibited in xrs-5 cells to a larger extent than in CHO cells after a similar exposure to heat. These results complement those previously reported on heat-induced radiosensitization in these cell lines, and suggest that the reduction in heat-induced radiosensitization observed in xrs-5 cells is largely due to their deficiency in repairing DNA dsb, rather than to a reduction in the ability of heat to inhibit DNA repair processes in general. The data presented here provide further support to the hypothesis that DNA dsb repair proficiency is a prerequisite for heat-induced radiosensitization.
在指数生长期或平台期的经照射的中国仓鼠卵巢(CHO)细胞及其DNA双链断裂修复缺陷型、辐射敏感型对应细胞xrs - 5细胞中,研究了热对DNA单链(ssb)和双链(dsb)断裂的诱导和修复的影响。通过碱性解旋技术测量DNA单链断裂的诱导和修复,而通过非解旋滤膜洗脱技术测量DNA双链断裂的诱导和修复。结果表明,在指数生长期或平台期生长的CHO或xrs - 5细胞中,预先将细胞暴露于45×5℃的热环境8 - 30分钟,并不影响每戈瑞辐射剂量及每道尔顿DNA所诱导产生的DNA单链断裂或双链断裂的数量。另一方面,预先暴露于热环境会抑制DNA修复过程,并增加照射后2小时所测得的未修复辐射诱导损伤的比例。在这两种细胞系中,DNA双链断裂的修复比DNA单链断裂的修复对热更敏感。在相似的热暴露后,xrs - 5细胞中辐射诱导的单链或双链断裂的修复比CHO细胞受到的抑制程度更大。这些结果补充了先前关于这些细胞系中热诱导放射增敏作用的报道,并表明在xrs - 5细胞中观察到的热诱导放射增敏作用的降低主要是由于它们在修复DNA双链断裂方面存在缺陷,而不是由于热抑制DNA修复过程的能力普遍下降。此处呈现的数据进一步支持了以下假设:DNA双链断裂修复能力是热诱导放射增敏作用的先决条件。