Schwartz H S, Kanter P M
Cancer Lett. 1981 Sep;13(4):309-13. doi: 10.1016/0304-3835(81)90059-8.
Leukemia cells from 4 acute myelocytic leukemia (AML) and 1 acute lymphocytic leukemia (ALL) patients were incubated with a set of 6 anthracycline agents: Adriamycin (Am), 4'-epi-Adriamycin (4'-epi-Am), daunorubicin (Dm), 4-demethoxy-daunorubicin (4-dDm), carminomycin (Cm) and N-trifluoroacetyl-Am-14-valerate (AD32). Cells were assayed for drug uptake after incubation for 2 h, and for DNA damage and drug retention 4 h later. Uptake and retention patterns were characteristic for each agent and fairly uniform for the different cell populations. In contrast, profiles of the amount of DNA damage produced reflected striking differences in each population of cells. These individual responses raise the possibility that leukemic cells resistant to one anthracycline may yet be sensitive to another.
来自4例急性髓细胞白血病(AML)患者和1例急性淋巴细胞白血病(ALL)患者的白血病细胞与一组6种蒽环类药物一起孵育:阿霉素(Am)、4'-表阿霉素(4'-epi-Am)、柔红霉素(Dm)、4-去甲氧基柔红霉素(4-dDm)、卡米诺霉素(Cm)和N-三氟乙酰阿霉素-14-戊酸酯(AD32)。孵育2小时后测定细胞对药物的摄取情况,4小时后测定DNA损伤和药物滞留情况。摄取和滞留模式对每种药物而言具有特征性,并且对于不同细胞群体相当一致。相比之下,所产生的DNA损伤量的概况反映出每个细胞群体存在显著差异。这些个体反应增加了一种可能性,即对一种蒽环类药物耐药的白血病细胞可能对另一种蒽环类药物仍敏感。