Waud W R
Kettering-Meyer Laboratory, Southern Research Institute, Birmingham, Alabama 35255.
Cancer Res. 1987 Dec 15;47(24 Pt 1):6549-55.
The uptake of cis-[14C]dichloro(ethylenediamine)platinum(II) (cis-DEP) is reduced in cis-diamminedichloroplatinum(II) (cis-DDP)-resistant L1210 cells [L1210/DDP (SRI)] in comparison to cis-DDP-sensitive L1210 cells (L1210/0). A difference in uptake is observed as early as 6 min after addition of cis-[14C]DEP and increases to approximately 3-fold after 30 min. This reduction in uptake is reflected in a decrease in the binding of platinum to DNA isolated from cis-DDP-treated cells as measured by atomic absorption spectroscopy and in the quantity of intracellular cis-DEP metabolites as measured by high-performance liquid chromatography. Similar differences in uptake are observed between ascitic L1210/0 and L1210/DDP (SRI) cells in vitro and in vivo, showing that the differences in uptake are not due to an artifact of the culturing process. The differences in cis-DEP uptake between the two cell lines were relatively unchanged during 7 mo in culture; however, both cell lines exhibited altered sensitivities to cis-DEP during extended culturing. No difference was observed in the efflux of cis-DEP by the two cell lines. Similarly, no difference in nonprotein and total sulfhydryl contents was observed between L1210/0 and L1210/DDP (SRI) cells. The difference in uptake (3-fold) of cis-DEP between L1210/0 and L1210/DDP (SRI) cells may not account fully for the observed differences in sensitivity of the two cell lines to cis-DDP (18-fold) and cis-DEP (19-fold). A portion of the resistance may be due to differences in the capacity of the two cell lines to survive in the presence of platinum damage.
与顺铂敏感的L1210细胞(L1210/0)相比,顺二氯二氨铂(II)(顺铂)耐药的L1210细胞[L1210/DDP(SRI)]中顺式-[14C]二氯(乙二胺)铂(II)(顺式-DEP)的摄取减少。早在加入顺式-[14C]DEP后6分钟就观察到摄取差异,30分钟后增加到约3倍。这种摄取减少反映在通过原子吸收光谱法测量的铂与从顺铂处理的细胞中分离的DNA的结合减少,以及通过高效液相色谱法测量的细胞内顺式-DEP代谢物的量减少。在体外和体内的腹水L1210/0和L1210/DDP(SRI)细胞之间观察到类似的摄取差异,表明摄取差异不是由于培养过程中的假象。两种细胞系之间顺式-DEP摄取的差异在培养7个月期间相对不变;然而,在延长培养期间,两种细胞系对顺式-DEP的敏感性均发生改变。两种细胞系对顺式-DEP的外排没有差异。同样,L1210/0和L1210/DDP(SRI)细胞之间在非蛋白质和总巯基含量方面没有差异。L1210/0和L1210/DDP(SRI)细胞之间顺式-DEP摄取的差异(3倍)可能无法完全解释观察到的两种细胞系对顺铂(18倍)和顺式-DEP(19倍)敏感性的差异。部分耐药性可能是由于两种细胞系在铂损伤存在下存活能力的差异。