Momparler R L, Karon M, Siegel S E, Avila F
Cancer Res. 1976 Aug;36(8):2891-5.
The effect of adriamycin on DNA, RNA, and protein synthesis was investigated in cell-free systems and intact cells. In studies with purified mammalian cell enzymes, adriamycin produced a greater inhibition of DNA-dependent DNA polymerase than of RNA polymerase. The extent of inhibition of both these enzymes was decreased by increasing the concentration of the DNA template in the reaction mixture. In studies with isolated nuclei, adriamycin was also a more potent inhibitor of DNA synthesis than RNA synthesis. However, with intact cells, adriamycin inhibited both DNA and RNA synthesis to about the same extent. The inhibition produced by adriamycin on RNA synthesis in intact cells was greater than that observed in the cell-free systems. Adriamycin inhibited protein synthesis in a cell-free system consisting of polyribosomes, transfer RNA, and enzymes but did not inhibit protein synthesis in intact cells. These differences in the pattern of inhibition may be due to biotransformation of the drug and/or preferential binding to chromosomal DNA in the intact cell.
在无细胞系统和完整细胞中研究了阿霉素对DNA、RNA和蛋白质合成的影响。在用纯化的哺乳动物细胞酶进行的研究中,阿霉素对依赖DNA的DNA聚合酶的抑制作用比对RNA聚合酶的抑制作用更强。通过增加反应混合物中DNA模板的浓度,这两种酶的抑制程度均降低。在用分离细胞核进行的研究中,阿霉素对DNA合成的抑制作用也比RNA合成更强。然而,对于完整细胞,阿霉素对DNA和RNA合成的抑制程度大致相同。阿霉素对完整细胞中RNA合成的抑制作用大于在无细胞系统中观察到的抑制作用。阿霉素在由多核糖体、转运RNA和酶组成的无细胞系统中抑制蛋白质合成,但在完整细胞中不抑制蛋白质合成。抑制模式的这些差异可能是由于药物的生物转化和/或在完整细胞中与染色体DNA的优先结合。