Weber G, Yamaji Y, Nagai M, Natsumeda Y, Jayaram H N, Zhen W N, Paulik E
Laboratory for Experimental Oncology, Indiana University School of Medicine, Indianapolis 46202-5200.
Adv Enzyme Regul. 1990;30:35-45. doi: 10.1016/0065-2571(90)90007-o.
New light was thrown on the action of tiazofurin in the treatment of end-stage leukemic patients and in leukemic cells in tissue culture. 1. In a population of 21 consecutive patients 50% responded to tiazofurin treatment, confirming the usefulness of this therapy in end-stage leukemia. 2. In leukemic patients treated with tiazofurin and allopurinol reciprocal action was manifested in the increase in hypoxanthine and the decrease in uric acid concentrations in the plasma. On discontinuation of allopurinol, hypoxanthine levels steeply declined but uric acid concentration increased slowly, taking days to reach pretreatment level. 3. With a new and sensitive method the concentration of the active metabolite of tiazofurin, TAD, was measured in the mononuclear cells of tiazofurin-treated patients. Approximately 5 to 13% of the plasma tiazofurin level was observed as TAD in the mononuclear cells. This TAD concentration was sufficient to account for the inhibition of IMP DH in these cells. 4. Tiazofurin or retinoic acid caused differentiation of HL-60 leukemic cells and inhibition of cell proliferation. 5. By treating leukemic cells incubated with tiazofurin or retinoic acid also with guanosine it was elucidated that the mechanism of the two drugs differed since only the tiazofurin effects were counteracted by guanosine. 6. Tiazofurin and retinoic acid together in HL-60 cells provided synergistic impact on differentiation and cytotoxicity. 7. Tiazofurin resulted in down-regulation of the expression of ras and myc oncogenes in three systems: K562 human erythroleukemic cells, rat hepatoma 3924A cells and human HL-60 leukemia cells. 8. Because both tiazofurin and retinoic acid are licensed drugs, their potential use in combination chemotherapy may have clinical relevance in the treatment of end-stage leukemia where our earlier studies have demonstrated the usefulness of tiazofurin.
关于硫唑嘌呤在治疗晚期白血病患者及组织培养中的白血病细胞方面的作用有了新的认识。1. 在连续21例患者中,50%对硫唑嘌呤治疗有反应,证实了该疗法在晚期白血病中的有效性。2. 在接受硫唑嘌呤和别嘌呤醇治疗的白血病患者中,血浆中次黄嘌呤增加、尿酸浓度降低体现了二者的相互作用。停用别嘌呤醇后,次黄嘌呤水平急剧下降,但尿酸浓度缓慢上升,需数天才能达到治疗前水平。3. 采用一种新的灵敏方法测定了硫唑嘌呤治疗患者单核细胞中硫唑嘌呤活性代谢物TAD的浓度。在单核细胞中观察到TAD浓度约为血浆硫唑嘌呤水平的5%至13%。该TAD浓度足以解释对这些细胞中肌苷酸脱氢酶的抑制作用。4. 硫唑嘌呤或维甲酸可导致HL-60白血病细胞分化并抑制细胞增殖。5. 通过用鸟苷处理与硫唑嘌呤或维甲酸一起孵育的白血病细胞发现,两种药物的作用机制不同,因为只有硫唑嘌呤的作用可被鸟苷抵消。6. 硫唑嘌呤和维甲酸共同作用于HL-60细胞时,对细胞分化和细胞毒性具有协同作用。7. 硫唑嘌呤导致ras和myc癌基因在三种细胞体系中表达下调:K562人红白血病细胞、大鼠肝癌3924A细胞和人HL-60白血病细胞。8. 由于硫唑嘌呤和维甲酸都是已获许可的药物,它们在联合化疗中的潜在应用在晚期白血病治疗中可能具有临床意义,我们早期的研究已证实硫唑嘌呤在该治疗中的有效性。