Hibino Y, Kamiuchi S, Kusashio E, Sugano N
Division of Cell Biology, Faculty of Pharmaceutical Sciences, Toyama Medical & Pharmaceutical University, Japan.
Biochem Mol Biol Int. 1996 Apr;38(5):973-9.
Rat-liver cells (Ac2F cells) were transfected with cisplatin-damaged eucaryotic expression vectors carrying luciferase cDNA (cis-DDP-pVJ3luc) and incubated. The lysate of the incubated cells was subjected to a luciferase activity assay. Graded decrease in the activity was observed with increasing levels of platination of the plasmid DNA. In another experiment, Ac2F cells were pre-incubated in the presence of cisplatin ranging in concentration from 0.5 to 3 mu M. The viable cells were transfected with cis-DDP-pVJ3luc and incubated in the absence of this drug. The lysate of the incubated cells was subjected to the same assay. The level of the luciferase activity was raised with increasing cisplatin concentration. These results suggest that the repair activity for cis-DDP-pVJ3luc DNA is enhanced in Ac2F cells exposed to cisplatin.
用携带荧光素酶cDNA的顺铂损伤真核表达载体(顺式-顺铂-pVJ3luc)转染大鼠肝细胞(Ac2F细胞)并进行孵育。对孵育细胞的裂解物进行荧光素酶活性测定。随着质粒DNA铂化水平的增加,观察到活性逐渐降低。在另一项实验中,将Ac2F细胞在浓度为0.5至3μM的顺铂存在下预孵育。用顺式-顺铂-pVJ3luc转染存活细胞,并在无此药物的情况下孵育。对孵育细胞的裂解物进行相同的测定。荧光素酶活性水平随着顺铂浓度的增加而升高。这些结果表明,在暴露于顺铂的Ac2F细胞中,对顺式-顺铂-pVJ3luc DNA的修复活性增强。