Tosi P, Zinzani P L, Pellacani A, Ottaviani E, Magagnoli M, Tura S
Institute of Hematology and Medical Oncology Seràgnoli University of Bologna, Policlinico S. Orsola, Italy.
Leuk Lymphoma. 1997 Jul;26(3-4):343-8. doi: 10.3109/10428199709051784.
Purine analogues like fludarabine have been shown to be superior to conventional therapy for B-cell chronic lymphocytic leukemia (B-CLL). In order to improve the activity of fludarabine, we tested its combination with loxoribine, a guanine ribonucleotide derivative, known to enhance the sensitivity of B-CLL cells to cytotoxic drugs. B-CLL cells from 6 patients were studied; co-incubation with loxoribine 100 microM increased the activity of fludarabine by 12% to 48%, as demonstrated by XTT colorimetric assay; while 1000 microM loxoribine exerted a protective effect. Accordingly, fludarabine-induced apoptosis was enhanced by the addition of loxoribine 1000 microM (39% increase). These results indicate that the combination of loxoribine and fludarabine could be of interest in B-CLL.
像氟达拉滨这样的嘌呤类似物已被证明在治疗B细胞慢性淋巴细胞白血病(B-CLL)方面优于传统疗法。为了提高氟达拉滨的活性,我们测试了它与洛索立宾(一种鸟嘌呤核糖核苷酸衍生物)的联合使用,已知该衍生物可增强B-CLL细胞对细胞毒性药物的敏感性。对6名患者的B-CLL细胞进行了研究;如XTT比色法所示,与100微摩尔的洛索立宾共同孵育可使氟达拉滨的活性提高12%至48%;而1000微摩尔的洛索立宾则发挥了保护作用。因此,添加1000微摩尔的洛索立宾可增强氟达拉滨诱导的细胞凋亡(增加39%)。这些结果表明,洛索立宾与氟达拉滨的联合使用可能对B-CLL有意义。