Marcovitch S, Keisari Y
Cancer Immunol Immunother. 1985;20(3):205-8. doi: 10.1007/BF00205577.
The anticancer drugs adriamycin (ADR) and actinomycin D (AMD) were tested for their effect on the oxidative burst (OB) of mouse peritoneal macrophages (MPM) and on the killing of tumor cells by OB-stimulated MPM. The oxidative burst of MPM determined by hydrogen peroxide (H2O2) production was severely impaired by ADR (10 micrograms/ml) and AMD (40 micrograms/ml) after a 1 h treatment and by lower concentrations of the drugs following a 24 h treatment. The toxicity of the drugs against MPM was comparable to their effect on EL4 cells. Pretreatment of EL4 and TLX-9 tumor cells with sublethal amounts of ADR for 4 h rendered the cells sensitive to the cytotoxic effect of OB-stimulated MPM which were otherwise unable to kill these cells. It seems that anticancer drugs and OB-stimulated macrophages can cooperate in the destruction of tumor cells in vitro.
对抗癌药物阿霉素(ADR)和放线菌素D(AMD)进行了测试,以研究它们对小鼠腹腔巨噬细胞(MPM)氧化爆发(OB)以及对经OB刺激的MPM杀伤肿瘤细胞能力的影响。经1小时处理后,ADR(10微克/毫升)和AMD(40微克/毫升)会严重损害通过过氧化氢(H2O2)生成量测定的MPM氧化爆发,而经24小时处理后,较低浓度的这些药物也会产生这种损害。这些药物对MPM的毒性与其对EL4细胞的作用相当。用亚致死量的ADR对EL4和TLX - 9肿瘤细胞进行4小时预处理,可使这些细胞对经OB刺激的MPM的细胞毒性作用敏感,否则MPM无法杀伤这些细胞。看来抗癌药物和经OB刺激的巨噬细胞在体外能够协同破坏肿瘤细胞。