Grindey G B, Moran R G
Cancer Res. 1975 Jul;35(7):1702-5.
The antitumor effects of methotrexate against early leukemia L1210 were partially reversed by the coadministration of allopurinol in vivo, even though allopurinol did not alter the growth-inhibitory effects of methotrexate against L1210 cells in culture. These data suggest that this alteration in antitumor activity results from a decreased catabolism of preformed systemic purines by allopurinol, a potent inhibitor of xanthine oxidase. On the other hand, the therapeutic effect of methotrexate against the P288 leukemia was not significantly altered by allopurinol did not significantly alter the toxicity of methotrexate that, in the mouse, the antileukemic effects of methotrexate are more related to a purineless rather than a thymineless death.
在体内,甲氨蝶呤对早期白血病L1210的抗肿瘤作用部分被别嘌呤醇的共同给药所逆转,尽管别嘌呤醇并未改变甲氨蝶呤在培养中对L1210细胞的生长抑制作用。这些数据表明,这种抗肿瘤活性的改变是由于别嘌呤醇(一种黄嘌呤氧化酶的有效抑制剂)减少了预先形成的全身性嘌呤的分解代谢。另一方面,别嘌呤醇并未显著改变甲氨蝶呤对P288白血病的治疗效果,也未显著改变甲氨蝶呤的毒性,即在小鼠中,甲氨蝶呤的抗白血病作用与无嘌呤死亡而非无胸腺嘧啶死亡更为相关。