Leibson P J, Schreiber H, Loken M R, Panem S, Rowley D A
Proc Natl Acad Sci U S A. 1978 Dec;75(12):6202-6. doi: 10.1073/pnas.75.12.6202.
We report that a chemotherapeutic agent (melphalan) can affect the sensitivity of tumor cells to cytotoxic antibody. Depending on the time interval between drug treatment and subsequent exposure to antibody and complement, the tumor cells can be either more resistant or more susceptible to antibody when compared to control cells. The number of tumor cells surviving the combined treatment was determined by a colony inhibition assay. The two antisera used in this study were directed against either virus-specific or myeloma protein-specific antigens on the surface of S107 murine myeloma cells; identical results were obtained with both sera. Twenty-four hours after exposure to the drug, the number of tumor cells surviving the antibody treatment increased. During this period of increased resistance, the tumor cells were temporarily arrested in the G(2) phase of the cell cycle. After this period of maximal resistance, the effect of cytotoxic antibody on the cells changed such that 4 days after melphalan treatment the cells were significantly more susceptible to the antibody than were the sham-treated control cells. The period of increased susceptibility correlated with an increased density of S107 myeloma protein and viral antigens on the surface of the tumor cells. Eight days after the drug treatment, the susceptibility of the tumor cells and the density of surface antigens both returned to normal levels. This study shows that the correct time interval between exposure to a drug and subsequent treatment with antibody is critical for maximal killing of the tumor cells. The basis for the differential sensitivity of the tumor cells to anti-body may be related to the drug-induced changes in the cell cycle and in antigen expression on the cell surface.
我们报告称,一种化疗药物(美法仑)可影响肿瘤细胞对细胞毒性抗体的敏感性。根据药物治疗与随后接触抗体及补体之间的时间间隔,与对照细胞相比,肿瘤细胞对抗体可能更具抗性或更敏感。联合治疗后存活的肿瘤细胞数量通过集落抑制试验确定。本研究中使用的两种抗血清分别针对S107小鼠骨髓瘤细胞表面的病毒特异性或骨髓瘤蛋白特异性抗原;两种血清均获得了相同的结果。接触药物24小时后,抗体治疗后存活的肿瘤细胞数量增加。在这种抗性增加的时期,肿瘤细胞暂时停滞在细胞周期的G(2)期。在这种最大抗性时期之后,细胞毒性抗体对细胞的作用发生了变化,使得美法仑治疗4天后,细胞对抗体的敏感性明显高于假处理的对照细胞。敏感性增加的时期与肿瘤细胞表面S107骨髓瘤蛋白和病毒抗原密度的增加相关。药物治疗8天后,肿瘤细胞的敏感性和表面抗原密度均恢复到正常水平。本研究表明,接触药物与随后用抗体治疗之间的正确时间间隔对于最大程度杀死肿瘤细胞至关重要。肿瘤细胞对抗体敏感性差异的基础可能与药物诱导的细胞周期变化和细胞表面抗原表达有关。