Yang J L, Cheng E H, Capizzi R L, Cheng Y C, Kute T
J Clin Invest. 1985 Jan;75(1):141-6. doi: 10.1172/JCI111666.
Pretreatment of L5178Y murine leukemia cells with uracil arabinoside (ara-U) enhances the cytotoxicity of cytosine arabinoside (ara-C). This effect is mediated by the cytostatic effect of ara-U, which causes a delay of cell progression through S-phase. Consequently, the specific activity of enzymes that peak during S-phase increases, and deoxycytidine kinase increases 3.6-fold over untreated controls. This allows enhanced anabolism of ara-C to nucleotides, as well as increased incorporation into DNA with ultimate synergistic cytotoxicity. It is postulated that the systemic metabolism of high-dose ara-C to sustained high levels of ara-U in patients with acute leukemia may enhance the activity of subsequent doses of ara-C, and thus contribute to a means for pharmacologic self-potentiation, contributing to the unique therapeutic activity of high-dose ara-C.
用阿糖尿苷(ara-U)预处理L5178Y小鼠白血病细胞可增强阿糖胞苷(ara-C)的细胞毒性。这种效应是由ara-U的细胞生长抑制作用介导的,它会导致细胞通过S期的进程延迟。因此,在S期达到峰值的酶的比活性增加,脱氧胞苷激酶比未处理的对照增加3.6倍。这使得ara-C向核苷酸的合成代谢增强,以及其掺入DNA增加,最终产生协同细胞毒性。据推测,急性白血病患者中高剂量ara-C全身代谢为持续高水平的ara-U可能会增强后续剂量ara-C的活性,从而有助于一种药理学自我增强的方式,这有助于高剂量ara-C独特的治疗活性。