Henne T, Berger M R
J Cancer Res Clin Oncol. 1986;111(1):75-8. doi: 10.1007/BF00402781.
Female Sprague-Dawley rats bearing methylnitrosourea-induced mammary carcinomas were treated with 100 mumol 1-(2-hydroxyethyl)-3-(2-chloroethyl)-3-nitrosourea (HECNU)/kg to investigate the time course of DNA-DNA interstrand cross-linking (DNA-XL) as measured by alkaline elution in tumor, bone marrow and liver cells. The inhibition of bone marrow stem cell colony formation in culture (CFU-C) and in spleens of lethally irradiated mice (CFU-S), serum transaminase levels and total bilirubin were concomitantly determined. All parameters were evaluated at different times from 4 to 72 h after treatment. The highest amounts of DNA-XL were found in tumor cells, peaking at 24 h after treatment. A parallel increase was observed in bone marrow cells up to 16 h with a subsequent rapid decrease to about one-third of DNA-XL in tumor cells after 72 h. Concomitantly, CFU-C and CFU-S were suppressed, the nadir being at 24 h after treatment. In liver cells, however, constant low levels of DNA-XL were found, which had disappeared after 48 h. In accordance with this observation, serum transaminase levels were only slightly elevated.
用100微摩尔1-(2-羟乙基)-3-(2-氯乙基)-3-亚硝基脲(HECNU)/千克对携带甲基亚硝基脲诱导的乳腺癌的雌性斯普拉格-道利大鼠进行治疗,以研究通过碱性洗脱法测定的肿瘤、骨髓和肝细胞中DNA-DNA链间交联(DNA-XL)的时间进程。同时测定培养的骨髓干细胞集落形成(CFU-C)和致死性照射小鼠脾脏中的集落形成单位(CFU-S)、血清转氨酶水平和总胆红素。在治疗后4至72小时的不同时间评估所有参数。在肿瘤细胞中发现最高量的DNA-XL,在治疗后24小时达到峰值。在骨髓细胞中观察到平行增加,直至16小时,随后在72小时后迅速下降至肿瘤细胞中DNA-XL的约三分之一。同时,CFU-C和CFU-S受到抑制,最低点出现在治疗后24小时。然而,在肝细胞中,发现DNA-XL的水平持续较低,在48小时后消失。根据这一观察结果,血清转氨酶水平仅略有升高。