Sadzuka Y, Iwazaki A, Sugiyama T, Sawanishi T, Miyamoto K
School of Pharmaceutical Sciences, University of Shizuoka, Yada.
Jpn J Cancer Res. 1998 Feb;89(2):228-33. doi: 10.1111/j.1349-7006.1998.tb00553.x.
We have screened xanthine derivatives for activity as novel biochemical modulators by assay of their inhibitory effect on adriamycin efflux from tumor cells. Strong inhibition of adriamycin efflux was shown by some xanthine derivatives with various alkyl or oxoalkyl substituents at the 1-, 3- and 7-positions. 1-Methyl-3-propyl-7-butylxanthine (XT-77), which had the greatest inhibitory effect on adriamycin efflux in vitro among the compounds tested, potentiated adriamycin-induced antitumor activity by causing an increase of adriamycin concentration in the tumor in vitro. Furthermore, XT-77 reduced the adverse drug reactions of adriamycin by decreasing the adriamycin concentrations in the heart and the liver. Thus, the combination of XT-77 with adriamycin not only increased the antitumor activity of adriamycin, but also decreased the adverse drug reactions.
我们通过检测黄嘌呤衍生物对阿霉素从肿瘤细胞中流出的抑制作用,筛选具有新型生化调节剂活性的黄嘌呤衍生物。一些在1、3和7位带有各种烷基或氧代烷基取代基的黄嘌呤衍生物对阿霉素流出表现出强烈抑制作用。在所测试的化合物中,1-甲基-3-丙基-7-丁基黄嘌呤(XT-77)在体外对阿霉素流出具有最大抑制作用,它通过在体外使肿瘤中阿霉素浓度升高来增强阿霉素诱导的抗肿瘤活性。此外,XT-77通过降低心脏和肝脏中的阿霉素浓度来减少阿霉素的药物不良反应。因此,XT-77与阿霉素联合使用不仅增强了阿霉素的抗肿瘤活性,还降低了药物不良反应。