Fergusson R J, Anderson L E, Macpherson J S, Robins P, Smyth J F
University Department of Clinical Oncology, Western General Hospital, Edinburgh, UK.
Br J Cancer. 1988 Apr;57(4):339-42. doi: 10.1038/bjc.1988.78.
The activity of a new nitrosourea (TCNU) based on the endogenous amino acid taurine was assessed in three human lung cancer xenografts growing in immunodeficient mice. Moderate activity (specific growth delays of 0.63 and 1.13 compared with controls) was seen in two non-small cell tumours after a single oral administration of 20 mg-1kg. This dose was curative in a small cell xenograft. By using high performance liquid chromatography it was possible to detect parent drug in the tumours as well as the plasma and tissues after oral administration of TCNU. Drug sensitivity was correlated inversely with the amount of the DNA repair enzyme 0(6)-methylguanine-DNA methyltransferase assayed from extracts of the tumour cells but not with the levels of parent drug within the tumour. This compound appears to have unique pharmacokinetic properties compared with other chloroethylnitrosoureas.
在免疫缺陷小鼠体内生长的三种人肺癌异种移植瘤中,对一种基于内源性氨基酸牛磺酸的新型亚硝基脲(TCNU)的活性进行了评估。单次口服20mg/kg后,在两种非小细胞肿瘤中观察到中等活性(与对照组相比,特定生长延迟分别为0.63和1.13)。该剂量对一种小细胞异种移植瘤具有治愈作用。通过高效液相色谱法,在口服TCNU后能够在肿瘤以及血浆和组织中检测到母体药物。药物敏感性与从肿瘤细胞提取物中检测到的DNA修复酶O(6)-甲基鸟嘌呤-DNA甲基转移酶的量呈负相关,但与肿瘤内母体药物的水平无关。与其他氯乙基亚硝基脲相比,该化合物似乎具有独特的药代动力学特性。