Bosland M C, Prinsen M K, Dirksen T J, Spit B J
Department of Biological Toxicology, TNO-CIVO Toxicology and Nutrition Institute, Zeist, The Netherlands.
Cancer Res. 1990 Feb 1;50(3):700-9.
Carcinomas of the rat prostate induced by a single injection of N-methyl-N-nitrosourea, 7,12-dimethylbenz(a)anthracene, and 3,2'-dimethyl-4-aminobiphenyl, after sequential treatment with cyproterone acetate and testosterone propionate, were evaluated as potential animal models for prostatic cancer. All ten carcinomas examined were located in the dorsolateral prostate region and did not involve the distal parts of the seminal vesicles and coagulating glands. The incidence of urinary obstruction leading to the animals' death was 6 of 10 rats, and metastases in the lung, abdominal lymph nodes, and/or liver also occurred in 6 of 10 rats. The tumors were invasive adenocarcinomas, showing frequent perineural invasion and a variable degree of differentiation. There were ultrastructural similarities with human prostatic carcinomas, such as intracellular lumina. Plasma acid phosphatase was increased. Enzyme histochemical analysis revealed similarities with the Dunning R3327H and -HI prostatic carcinomas but was not helpful in determining the site of origin of the tumors. The gross and microscopic appearance of the tumors and the observation of preneoplastic lesions exclusively located in the dorsolateral prostate suggest this lobe as site of origin of the carcinomas. Preneoplastic lesions (n = 9) included atypical hyperplasias (n = 5) and lesions with all histological characteristics of carcinoma except for local invasion and metastases, which were classified as carcinoma in situ (n = 4). Although androgen sensitivity could not be assessed, the observed characteristics of the tumors [their long latency time (46-80 weeks), the presence of preneoplastic lesions, and the short duration of the treatment, leaving the animals intact] all indicate that the present approach is a valid animal model for the study of prostatic carcinogenesis.
单次注射N-甲基-N-亚硝基脲、7,12-二甲基苯并(a)蒽和3,2'-二甲基-4-氨基联苯诱导大鼠前列腺癌后,经醋酸环丙孕酮和丙酸睾酮序贯治疗,将其评估为前列腺癌的潜在动物模型。检查的所有10例癌均位于背外侧前列腺区域,未累及精囊远端和凝固腺。导致动物死亡的尿路梗阻发生率为10只大鼠中的6只,10只大鼠中有6只还发生了肺、腹部淋巴结和/或肝脏转移。肿瘤为浸润性腺癌,常伴有神经周围浸润,分化程度不一。与人类前列腺癌存在超微结构相似性,如细胞内管腔。血浆酸性磷酸酶升高。酶组织化学分析显示与邓宁R3327H和-HI前列腺癌相似,但无助于确定肿瘤的起源部位。肿瘤的大体和显微镜下表现以及仅位于背外侧前列腺的癌前病变观察表明该叶为癌的起源部位。癌前病变(n = 9)包括非典型增生(n = 5)和除局部浸润和转移外具有癌的所有组织学特征的病变,后者被归类为原位癌(n = 4)。尽管无法评估雄激素敏感性,但肿瘤的观察特征[其长潜伏期(46 - 80周)、癌前病变的存在以及治疗时间短,动物保持完整]均表明本方法是研究前列腺癌发生的有效动物模型。