Rockwell S, Keyes S R, Sartorelli A C
Department of Therapeutic Radiology, Yale University School of Medicine, New Haven, Connecticut 06510-8040.
Anticancer Res. 1989 Jul-Aug;9(4):817-20.
The effects of dicoumarol (DIC) on the cytotoxicity of porfiromycin (POR) were studied in vitro using EMT6 mammary tumor cells in monolayer cultures and in vivo using solid EMT6 tumors and bone marrow stem cells. In vitro, POR was more toxic to hypoxic EMT6 cells than to aerobic cells. Exposure of aerobic cultures to DIC protected against POR; in contrast, DIC sensitized hypoxic cells to POR. Treatment of mice with DIC produced a slight increase in the toxicity of POR to cells in solid tumors. The toxicity of POR to marrow stem cells (CFU-GM and CFU-MK) was not altered by DIC. Pretreatment of mice with DIC therefore produced a small improvement in the therapeutic ratio.
使用单层培养的EMT6乳腺肿瘤细胞在体外研究双香豆素(DIC)对卟吩姆钠(POR)细胞毒性的影响,并使用实体EMT6肿瘤和骨髓干细胞在体内进行研究。在体外,POR对缺氧的EMT6细胞比需氧细胞毒性更大。将需氧培养物暴露于DIC可防止POR的毒性;相反,DIC使缺氧细胞对POR敏感。用DIC处理小鼠会使POR对实体瘤细胞的毒性略有增加。DIC不会改变POR对骨髓干细胞(CFU-GM和CFU-MK)的毒性。因此,用DIC预处理小鼠可使治疗比率略有提高。