Mandelbaum-Shavit F, Ramu A
Cell Biol Int Rep. 1987 May;11(5):389-96. doi: 10.1016/0309-1651(87)90006-3.
P388 murine leukemia cells 18.4-fold more resistant to methotrexate (MTX) than the parent, drug susceptible line, were shown to possess a 1.5-fold higher dihydrofolate reductase (EC1.5.1.3) (DHFR) activity. This is in contrast to a MTX-resistant line, obtained from adriamycin-resistant cells, which is 27.9-fold more resistant to MTX and exhibits a 22.4-fold higher DHFR activity than that of the parent. The susceptibility of the enzyme to inhibition by MTX does not markedly change with the acquired drug resistance of the cell lines studied. Thus MTX-resistant cells obtained from an adriamycin-resistant line acquired resistance due to increased activity of the target enzyme, whereas other mechanisms are responsible for the resistance of cells derived from the adriamycin-sensitive parent.
P388鼠白血病细胞对甲氨蝶呤(MTX)的抗性比亲本药物敏感细胞系高18.4倍,其二氢叶酸还原酶(EC1.5.1.3)(DHFR)活性比亲本高1.5倍。这与从阿霉素抗性细胞获得的MTX抗性细胞系形成对比,该细胞系对MTX的抗性高27.9倍,其DHFR活性比亲本高22.4倍。在所研究的细胞系获得耐药性后,该酶对MTX抑制的敏感性没有明显变化。因此,从阿霉素抗性细胞系获得的MTX抗性细胞是由于靶酶活性增加而获得抗性,而源自阿霉素敏感亲本的细胞的抗性则由其他机制所致。