Houghton J A, Houghton P J
Cancer Treat Rep. 1982 May;66(5):1201-6.
A series of four human colon adenocarcinomas, growing as xenografts in immune-deprived mice, have been used to evaluate the efficacy of 5-FU in combination with two purines, hypoxanthine (Hx) and allopurinol (HPP), which have reduced the toxicity of 5-FU in host mice. Tumor-bearing mice were treated at 7-day intervals with 5-FU administered simultaneously with the protecting agents (Hx and HPP). Two tumor lines (HxVRC5 and HxGC3), insensitive to 5-FU alone, failed to show any response to this combination. In 5-FU-sensitive HxELC2 tumors, the combination of 5-FU with Hx and HPP did not increase the therapeutic index, and in HxHC1 xenografts, antagonism to 5-FU cytotoxicity was observed. Tumor response in relation to the pathways of 5-FU metabolism is discussed.
将4个人类结肠腺癌作为异种移植物在免疫缺陷小鼠体内生长,用于评估5-氟尿嘧啶(5-FU)与两种嘌呤(次黄嘌呤(Hx)和别嘌呤醇(HPP))联合使用的疗效,这两种嘌呤可降低5-FU对宿主小鼠的毒性。荷瘤小鼠每隔7天接受一次5-FU治疗,同时给予保护剂(Hx和HPP)。两个单独对5-FU不敏感的肿瘤系(HxVRC5和HxGC3)对这种联合治疗没有任何反应。在对5-FU敏感的HxELC2肿瘤中,5-FU与Hx和HPP联合使用并未提高治疗指数,而在HxHC1异种移植物中,观察到对5-FU细胞毒性的拮抗作用。讨论了肿瘤反应与5-FU代谢途径的关系。