Takemiya M, Miyayama H, Takeuchi T
Acta Pathol Jpn. 1982 Mar;32(2):257-64. doi: 10.1111/j.1440-1827.1982.tb02047.x.
Seventy four white male Wistar rats were divided into two groups and given weekly subcutaneous injections of 30 mg 1,2-dimethylhydrazine (DMH) 2HC1/kg body weight for 10 or 15 weeks, respectively, and the histological properties and distribution of DMH-induced rat carcinomas were investigated. The carcinomas induced by DMH were classified mainly into mucin producing carcinomas and non-mucin producing ones. In the large intestine, the group treated for 15 weeks induced significant incidences of mucin producing carcinomas composed mainly of cells containing intracellular mucin. Mucin producing carcinomas consisted of poorly differentiated adenocarcinoma, signet ring cell carcinoma and mucinous carcinoma, and these often coexisted within the same tumor mass. Mucin producing carcinomas tended to develop in the proximal colon and caecum, while non-mucin producing carcinomas were frequent in the distal colon. This method was thought to be a useful model to study glycoproteins of cancer cells.
74只雄性Wistar大白鼠被分为两组,分别连续10周或15周每周皮下注射30毫克1,2 - 二甲基肼(DMH)2HC1/千克体重,然后研究DMH诱导的大鼠癌的组织学特性和分布。DMH诱导的癌主要分为产生黏液的癌和不产生黏液的癌。在大肠中,接受15周治疗的组中产生黏液的癌发生率显著增加,这些癌主要由含有细胞内黏液的细胞组成。产生黏液的癌包括低分化腺癌、印戒细胞癌和黏液癌,这些类型常常在同一肿瘤块中共存。产生黏液的癌倾向于发生在近端结肠和盲肠,而不产生黏液的癌在远端结肠更为常见。该方法被认为是研究癌细胞糖蛋白的有用模型。