McCulloch E A, Kelleher C A, Miyauchi J, Wang C, Cheng G Y, Minden M D, Curtis J E
Division of Biological Research, Ontario Cancer Institute, Toronto, Canada.
Leukemia. 1988 Dec;2(12 Suppl):38S-49S.
Morphological-identified blast populations are the hallmark of the malignant clones that dominate hemopoiesis in acute myeloblastic leukemia (AML). Marked heterogenity is characteristic of AML blasts. Patient-to-patient variation is seen in their biological properties but is particularly evident in the response to treatment. Intraclonal variation is generated during clonal expansion, particularly as blast stem cells either undergo self-renewal or enter into a series of terminal divisions. These two alternative activities can be monitored in cell culture using a clonogenic assay and a suspension assay. The balance between renewal and differentiation can be altered by exposing blast populations to various growth factors in culture. Further, certain drugs, particularly ara-C, appear to be more toxic for self-renewing divisions than cell-cycle events generally. We suggest that both drugs and growth factors should be assessed for their effects on self-renewal as part of preclinical testing.
形态学鉴定的原始细胞群体是急性髓系白血病(AML)中主导造血的恶性克隆的标志。AML原始细胞具有明显的异质性。患者之间在生物学特性上存在差异,但在对治疗的反应中尤为明显。克隆内变异在克隆扩增过程中产生,特别是当原始干细胞进行自我更新或进入一系列终末分裂时。这两种替代活动可以在细胞培养中使用克隆形成试验和悬浮试验进行监测。通过在培养中将原始细胞群体暴露于各种生长因子,可以改变更新与分化之间的平衡。此外,某些药物,特别是阿糖胞苷,似乎对自我更新分裂的毒性比对一般细胞周期事件的毒性更大。我们建议,作为临床前测试的一部分,应评估药物和生长因子对自我更新的影响。