Sinha S, Hockin L J, Neal G E
Br J Cancer. 1987 Jun;55(6):595-8. doi: 10.1038/bjc.1987.121.
Aflatoxin B1 (AFB1) induced rat liver cancer is a well studied system of hepatocarcinogenesis. AFB1 has also been used to transform cultured rat liver derived cells in vitro. Cells in culture often have a reduced capacity to metabolise the AFB1 to its active metabolite, and often prolonged periods of exposure to the toxin have to be employed, with a long latency in the appearance of transformed cells in culture. We report here the transformation of a rat liver derived cell line by acute treatment with AFB1. An extrinsic metabolising system of quail microsomes, which convert AFB1 to its epoxide form with high efficiency, was used to activate the AFB1. A dose dependent cytotoxicity was obtained and neoplastic transformation was seen in the higher doses used. The enzyme GGT which has strong association with liver cell transformation both in vivo and in vitro was also elevated in the treated cells.
黄曲霉毒素B1(AFB1)诱导的大鼠肝癌是一个经过充分研究的肝癌发生系统。AFB1也被用于体外转化培养的大鼠肝脏来源细胞。培养中的细胞代谢AFB1为其活性代谢物的能力通常会降低,并且常常需要长时间暴露于该毒素,培养中转化细胞出现的潜伏期很长。我们在此报告通过用AFB1急性处理对大鼠肝脏来源细胞系的转化。鹌鹑微粒体的外源性代谢系统可高效地将AFB1转化为其环氧化物形式,用于激活AFB1。获得了剂量依赖性细胞毒性,并且在使用的较高剂量中观察到肿瘤转化。在体内和体外都与肝细胞转化密切相关的γ-谷氨酰转移酶(GGT)在处理过的细胞中也升高了。