Stoica G, Koestner A, Capen C C
Anticancer Res. 1984 Jan-Apr;4(1-2):5-12.
Intraperitoneal administration of high doses (45, 90, and 180 mg/kg of ENU (N-ethyl-N-nitrosourea) to 30-day-old female Sprague-Dawley (CD) rats resulted in a high incidence (greater than 100%) of mammary tumors (MT), of which 95% were malignant. The mean induction time was 92 days for the high dose group. There was a definite dose-effect relationship. As the dose of ENU decreased the number of rats affected and number of tumors per rat decreased, but the survival time and mean induction time increased. At the time of death 7.5% of mammary tumors had metastasized to the lung. A variety of histological MT types were produced simulating breast tumors in women. In addition to MT, a number of rats developed primary tumors in other organs (brain, ovary, kidney, and hemic-lymphatic system). The high MT incidence, high rate of malignancy, short latent period, and the simulation of human breast tumor types suggest this experimental design to be a valuable animal model to study initiation, hormone dependency, and pathogenesis of mammary neoplasia.
给30日龄雌性斯普拉格-道利(CD)大鼠腹腔注射高剂量(45、90和180毫克/千克N-乙基-N-亚硝基脲(ENU)),导致乳腺肿瘤(MT)的高发病率(超过100%),其中95%为恶性肿瘤。高剂量组的平均诱发时间为92天。存在明确的剂量效应关系。随着ENU剂量的降低,受影响的大鼠数量和每只大鼠的肿瘤数量减少,但存活时间和平均诱发时间增加。在死亡时,7.5%的乳腺肿瘤已转移至肺部。产生了多种组织学类型的乳腺肿瘤,模拟了人类的乳腺肿瘤。除乳腺肿瘤外,一些大鼠在其他器官(脑、卵巢、肾和血液淋巴系统)发生了原发性肿瘤。乳腺肿瘤的高发病率、高恶性率、短潜伏期以及对人类乳腺肿瘤类型的模拟表明,该实验设计是研究乳腺肿瘤发生、激素依赖性和发病机制的有价值的动物模型。