Herman T S
Cancer Res. 1983 Feb;43(2):517-20.
We have examined the effect of mildly hypothermic temperatures (22-32 degrees) on the cytotoxicity of Adriamycin, cis-diamminedichloroplatinum, bleomycin, and 1,3-bis(2-chloroethyl)-1-nitrosourea in Chinese hamster ovary cells in vitro. Over a dose range of Adriamycin, cell killing at 30 degrees was reduced by 1 to 3 orders of magnitude as compared to that at 37 degrees. cis-Diamminedichloroplatinum was also less cytotoxic at 30 degrees (0.4 to 1.2 orders of magnitude) than at 37 degrees. For bleomycin and 1,3-bis(2-chloroethyl)-1-nitrosourea, the reduction in cytotoxicity at 30 degrees in comparison to 37 degrees was less marked. All drugs were more toxic at 42.4-43 degrees than at 37 degrees. Precooling of cells for 2 hr at 30 degrees did not alter the cell killing caused by these drugs at elevated temperatures. These results suggest that a more selective anticancer effect might result if some chemotherapeutic drugs were administered during whole-body hypothermia and regional-local hyperthermia of tumor masses.
我们研究了轻度低温(22 - 32摄氏度)对阿霉素、顺二氨二氯铂、博来霉素和1,3 - 双(2 - 氯乙基)- 1 - 亚硝基脲在中国仓鼠卵巢细胞体外细胞毒性的影响。在阿霉素的剂量范围内,与37摄氏度相比,30摄氏度时细胞杀伤减少了1至3个数量级。顺二氨二氯铂在30摄氏度时的细胞毒性也比37摄氏度时小(0.4至1.2个数量级)。对于博来霉素和1,3 - 双(2 - 氯乙基)- 1 - 亚硝基脲,与37摄氏度相比,30摄氏度时细胞毒性的降低不太明显。所有药物在42.4 - 43摄氏度时比37摄氏度时毒性更大。将细胞在30摄氏度下预冷2小时不会改变这些药物在高温下引起的细胞杀伤。这些结果表明,如果在全身低温和肿瘤块区域局部高温期间给予某些化疗药物,可能会产生更具选择性的抗癌效果。