Nakajima Y, Miyamoto T, Tanabe M, Watanabe I, Terasima T
Cancer Res. 1979 Sep;39(9):3763-7.
The enhanced cytocidal effect of a combination of X-rays and 5-fluorouracil was investigated by means of colony-forming ability in mouse L-cells. Cells were treated with 5-fluorouracil immediately preceding (preirradiation treatment) or following (postirradiation treatment) irradiation. In either pre- or postirradiation treatment with various concentrations of the drug for a fixed time, the enhanced effect was augmented with increasing concentrations of 5-fluorouracil up to 20 microgram/ml. When cells were subjected to postirradiation treatment with a fixed concentration of drug for varying times, the cytocidal effect was further enhanced with increasing duration of drug treatment. In preirradiation treatment, however, drug treatment for longer than 3 hr did not exhibit any further enhancement. Postirradiation treatment with 5-fluorouracil to synchronous cells at various ages demonstrated enhancement at all ages during the cell cycle. The greatest enhancement was observed in the DNA-synthetic phase. Postirradiation treatment with 5-fluorouracil (2.5 microgram/ml) for 24 hr markedly reduced the width of the shoulder of the X-ray survival curve without significantly altering the slope of the exponential portion of the curve. Recovery from sublethal radiation damage was not suppressed by 5-fluorouracil when cells were treated with drug between fractionated X-ray doses. These results indicate that damages caused by 5-fluorouracil and X-rays interact additively to induce cell killing.
通过小鼠L细胞的集落形成能力研究了X射线与5-氟尿嘧啶联合使用时增强的杀细胞效应。细胞在照射前(照射前处理)或照射后(照射后处理)立即用5-氟尿嘧啶处理。在照射前或照射后用不同浓度的药物处理固定时间,增强效应随着5-氟尿嘧啶浓度增加至20微克/毫升而增强。当细胞用固定浓度的药物进行照射后处理不同时间时,杀细胞效应随着药物处理时间延长而进一步增强。然而,在照射前处理中,药物处理超过3小时未显示出任何进一步增强。对不同年龄的同步细胞进行5-氟尿嘧啶照射后处理表明,在细胞周期的所有阶段均有增强。在DNA合成期观察到最大增强。用5-氟尿嘧啶(2.5微克/毫升)进行照射后处理24小时,显著降低了X射线存活曲线的肩部宽度,而未显著改变曲线指数部分的斜率。当细胞在分次X射线剂量之间用药物处理时,5-氟尿嘧啶并未抑制亚致死性辐射损伤的恢复。这些结果表明,5-氟尿嘧啶和X射线造成的损伤相互作用,以诱导细胞死亡。