Moore M A, Nakagawa K, Ishikawa T
Department of Experimental Pathology, Cancer Institute, Tokyo.
Jpn J Cancer Res. 1988 Feb;79(2):187-94. doi: 10.1111/j.1349-7006.1988.tb01576.x.
Development of glutathione S-transferase placental form (GST-P)-positive focal populations was investigated subsequent to single injections of the hepatocarcinogens aflatoxin B1 (AfB1), dimethylnitrosamine (DMN) and diethylnitrosamine (DEN). While DEN proved far more potent at inducing putative initiated hepatocytes, the AfB1 treatment was associated with a very rapid (3 weeks) development of lesions approaching nodular proportions. Autoradiographic investigation revealed selective incorporation of label into GST-P-positive hepatocytes and oval cells at the day 7 time point following AfB1 treatment. Administration of butylated hydroxyanisole (BHA) subsequent to carcinogen injection was associated with a decrease in the final yield of lesions and increased tritiated thymidine incorporation in perivenular zone 3 background hepatocytes. The results suggest that 'selection pressure', resulting in rapid growth and development of putative preneoplastic lesions, is inherent in a single injection of the mycotoxin and indicate that variations of the present short-term model may be useful for elucidating the mechanisms underlying AfB1-induced hepatocarcinogenesis.
在单次注射肝癌致癌物黄曲霉毒素B1(AfB1)、二甲基亚硝胺(DMN)和二乙基亚硝胺(DEN)之后,对谷胱甘肽S-转移酶胎盘型(GST-P)阳性灶性群体的发育情况进行了研究。虽然DEN在诱导假定的起始肝细胞方面被证明效力更强,但AfB1处理与病变在非常短的时间(3周)内发展到接近结节大小有关。放射自显影研究显示,在AfB1处理后第7天,标记物选择性地掺入GST-P阳性肝细胞和卵圆细胞中。在注射致癌物后给予丁基羟基茴香醚(BHA),与病变的最终产量降低以及3区中央静脉周围背景肝细胞中氚标记胸腺嘧啶核苷掺入增加有关。结果表明,单次注射这种霉菌毒素会产生“选择压力”,导致假定的癌前病变快速生长和发展,这表明当前短期模型的变体可能有助于阐明AfB1诱导肝癌发生的潜在机制。