Pozharisski K M
J Natl Cancer Inst. 1975 May;54(5):1115-35. doi: 10.1093/jnci/54.5.1115.
In a morphogenetic study of experimental tumors of the intestine, 556 male noninbred albino rats were given weekly sc injections of 21 mg 1, 2-dimethylhydrazine dihydrochloride/kg body weight and were killed at different intervals (10-70 rats/wk) after the beginning of treatment. Intestinal carcinomas developed in almost all rats surviving 5 months after the beginning of the experiment. In addition, intestinal tumors induced in 800 rats of both sexes were examined. Tumor development began with a widening of the proliferative zone within the crypts, an indication of enterocyte differentiation disorders. The ensuing in situ carcinoma became superficial cancer capable of invading the lamina propria of the mucosa. Its continued growth caused the tumor to penetrate the tunica muscularis mucosae into the underlying layers of the intestinal wall. Thus experimental intestinal adenocarcinomas developed de novo or, at least, were not preceded by adenomatous polyps. Signet-ring cell carcinomas began with the accumulation of goblet cells in cells of signet-ring appearance; later they ruptured the basal membrane and infiltrated the surrounding tissues. The proposed scheme of morphogenesis of experimental tumors was correlated with current concepts of rectal tumor development in man.
在一项关于实验性肠道肿瘤的形态发生学研究中,给556只雄性非近交系白化大鼠每周皮下注射21毫克盐酸1,2 - 二甲基肼/千克体重,并在开始治疗后的不同间隔时间(每周10 - 70只大鼠)处死。几乎所有在实验开始后存活5个月的大鼠都发生了肠道癌。此外,还检查了800只雌雄大鼠诱导产生的肠道肿瘤。肿瘤的发展始于隐窝内增殖区的增宽,这表明肠上皮细胞分化紊乱。随后原位癌发展为能够侵犯黏膜固有层的浅表癌。其持续生长导致肿瘤穿透黏膜肌层进入肠壁的下层。因此,实验性肠道腺癌是从头发生的,或者至少在之前没有腺瘤性息肉。印戒细胞癌始于杯状细胞在印戒样细胞中的聚集;随后它们破坏基底膜并浸润周围组织。所提出的实验性肿瘤形态发生方案与当前关于人类直肠肿瘤发展的概念相关。