Horikoshi A, Smith R, Murphy M J
Chemotherapy. 1983;29(2):135-44. doi: 10.1159/000238187.
Comparative studies to determine the suppressive effects of chlorozotocin (2-[3-(2-chloroethyl)-3-nitrosoureido]-D-glucopyranose) and BCNU (1,3-bis[2-chloroethyl]-1-nitrosourea) on mouse and human hematopoietic precursor cells: granulocyte-macrophage precursor cells (CFU-gm), late erythroid precursor cells (CFU-e), and early erythroid precursor cells (BFU-e) were performed after in vitro incubation of 1 h with drug concentrations based on clinical administration levels. The suppressive effect of chlorozotocin on CFU-gm, BFU-e, and CFU-e hematopoietic precursor cells in the mouse was less than that of BCNU with the most significant difference seen in CFU-e colony formation. For human hematopoietic progenitor cells, however, the suppressive effect of chlorozotocin was far less than that of BCNU. When the effects of 40 micrograms/ml of chlorozotocin and 20 micrograms/ml of BCNU on human marrow were compared, there were statistically significant differences found for CFU-gm colony formation, and BFU-e and CFU-e colony numbers were significantly different for the two drugs at all comparable concentrations tested. Our results confirm the clinical data, and establish that the effects of chlorozotocin on human hematopoietic precursor cells are minimal.
为确定氯脲霉素(2-[3-(2-氯乙基)-3-亚硝基脲基]-D-吡喃葡萄糖)和卡氮芥(1,3-双[2-氯乙基]-1-亚硝基脲)对小鼠和人类造血前体细胞的抑制作用而进行的对比研究:粒细胞-巨噬细胞前体细胞(CFU-gm)、晚期红系前体细胞(CFU-e)和早期红系前体细胞(BFU-e)在根据临床给药水平设置的药物浓度下体外孵育1小时后进行检测。氯脲霉素对小鼠CFU-gm、BFU-e和CFU-e造血前体细胞的抑制作用小于卡氮芥,在CFU-e集落形成方面差异最为显著。然而,对于人类造血祖细胞,氯脲霉素的抑制作用远小于卡氮芥。当比较40微克/毫升氯脲霉素和20微克/毫升卡氮芥对人类骨髓的作用时,发现CFU-gm集落形成存在统计学显著差异,并且在所有测试的可比浓度下,两种药物的BFU-e和CFU-e集落数量均存在显著差异。我们的结果证实了临床数据,并确定氯脲霉素对人类造血前体细胞的作用极小。