Hyperthermic Potentiation of Unrejoined DNA Strand Breaks Following Irradiation

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Abstract
Previous reports have suggested that the potentiation of cellular radiation sensitivity by hyperthermia may be due to its inhibition of the repair of single-strand breaks in DNA. Such inhibition could result in increased numbers of unrejoined breaks at long times following irradiation, lesions that are presumed to be lethal to the cell. As a test of this hypothesis, the amounts of residual strand-break damage in [Chinese hamster ovary] cells following combined hyperthermia and ionizing radiation were measured. The results show that hyperthermia does significantly enhance the relative number of unrejoined strand breaks as measured by the technique of alkaline elution and that the degree of enhancement is dependent on both the temperature and duration of the hyperthermia treatment. Compared to unheated cells, the proportion of unrejoined breaks measured 8 h after irradiation was increased by a factor of 1.5 in cells that were treated for 30 min at 43.degree. C, by a factor of 6 for cells treated for 30 min at 45.degree. C, and by a factor of 4 for cells treated at 43.degree. C for 2 h. In experiments in which the sequence of heat and irradiation were varied, a high degree of correlation was observed between the resulting level of cell killing and the relative numbers of unrejoined strand breaks. The greatest effects on both of these parameters were observed in those protocols in which the irradiation was delivered either during, just before, or just after the heat treatment. [This study has applications for cancer treatment.].