Kimler B F, Henderson S D, Mansfield C M, Svoboda D J, Cheng C C
Cancer Res. 1982 Jul;42(7):2656-9.
Dihydroxyanthraquinone (DHAQ; NSC 279836) is a recently synthesized compound that is structurally similar to Adriamycin and produces greater antitumor effects in murine model systems. We compared DHAQ to Adriamycin in rats, with and without irradiation of the chest at various intervals after drug treatment. A single injection of Adriamycin (1 mg/kg i.p.) had little effect on animal survival, even if combined with radiation (12 Gy 25 MV X-rays), greater than 90% being alive at 1 year. A single injection of DHAQ (3 mg/kg i.p.) was equally uneffective up to 200 days after treatment (survival, greater than 90%). However, between 200 and 370 days after treatment, all animals died, producing a median survival time of 280 days. Further, when DHAQ was combined with radiation, there was an increase in animal deaths between Days 300 and 200. For animals irradiated on Days 0, 43, and 93 after DHAQ treatment, only 50, 75, and 80%, respectively, survived to Day 200. All animals that survived past Day 200 subsequently died by 1 year, displaying the same kinetics of lethality as those animals that had received DHAQ only. A repeat experiment using DHAQ at 1 mg/kg produced similar results. Based on these findings, we conclude that DHAQ produces a long-term (greater than 200 days) toxicity in rats that is not detectable by short-duration toxicity screening. In addition, radiation enhances short-term (less than 200 days) lethality, with the degree of enhancement decreasing as the interval between drug and radiation is increased.
二羟基蒽醌(DHAQ;NSC 279836)是一种最近合成的化合物,其结构与阿霉素相似,在小鼠模型系统中产生更大的抗肿瘤作用。我们在大鼠中比较了DHAQ和阿霉素,在药物治疗后的不同时间间隔对胸部进行或不进行照射。单次注射阿霉素(1mg/kg腹腔注射)对动物存活几乎没有影响,即使与辐射(12Gy 25MV X射线)联合使用,1年后仍有超过90%的动物存活。单次注射DHAQ(3mg/kg腹腔注射)在治疗后200天内同样无效(存活率大于90%)。然而,在治疗后200至370天之间,所有动物死亡,中位存活时间为280天。此外,当DHAQ与辐射联合使用时,在第200天至300天之间动物死亡增加。对于在DHAQ治疗后第0、43和93天接受照射的动物,分别只有50%、75%和80%存活至第200天。所有存活超过第200天的动物随后在1年内死亡,显示出与仅接受DHAQ治疗的动物相同的致死动力学。使用1mg/kg DHAQ的重复实验产生了类似的结果。基于这些发现,我们得出结论,DHAQ在大鼠中产生长期(大于200天)毒性,短期毒性筛选无法检测到。此外,辐射增强了短期(小于200天)致死率,随着药物与辐射之间间隔的增加,增强程度降低。