Arundel C M, Nishioka K, Tofilon P J
Department of Experimental Radiotherapy, University of Texas System Cancer Center, M. D. Anderson Hospital & Tumor Institute, Houston 77030.
Radiat Res. 1988 Jun;114(3):634-40.
The effect of the polyamine biosynthesis inhibitor alpha-difluoromethylornithine (DFMO) on the in vitro radiation response of Clone A human colon adenocarcinoma cells was investigated. Analysis of intracellular polyamine levels showed that exposure of Clone A cells to 1 mM DFMO for 96 h reduced putrescine and spermidine to nondetectable levels, while spermine was decreased by approximately 50%. This DFMO treatment protocol enhanced the radiosensitivity of Clone A cells, which was reflected by a decrease in both the Do and Dq. The addition of putrescine (1 mM) for the final 48 h of DFMO exposure restored polyamine levels and returned clone A radiosensitivity to that of control cells. These results indicate that polyamine depletion by DFMO sensitizes Clone A tumor cells to ionizing radiation.
研究了多胺生物合成抑制剂α-二氟甲基鸟氨酸(DFMO)对克隆A人结肠腺癌细胞体外辐射反应的影响。细胞内多胺水平分析表明,将克隆A细胞暴露于1 mM DFMO 96小时可使腐胺和亚精胺降至无法检测的水平,而精胺减少约50%。这种DFMO处理方案增强了克隆A细胞的放射敏感性,这通过Do和Dq的降低得以体现。在DFMO暴露的最后48小时添加腐胺(1 mM)可恢复多胺水平,并使克隆A细胞的放射敏感性恢复至对照细胞水平。这些结果表明,DFMO导致的多胺耗竭使克隆A肿瘤细胞对电离辐射敏感。