Tahir M K, Guthenberg C, Mannervik B
Department of Biochemistry, Arrhenius Laboratory, University of Stockholm, Sweden.
Biochem J. 1989 Jan 1;257(1):215-20. doi: 10.1042/bj2570215.
Rat hepatoma cells grown intraperitoneally as an ascites tumour were analysed with respect to their contents of cytosolic glutathione transferases. In contrast with normal liver tissue, the hepatoma cells were dominated by the class Pi glutathione transferase 7-7. All the major hepatic enzyme forms were down-regulated to almost undetectable concentrations. Livers of rats bearing ascites-hepatoma cells expressed low, but significant, amounts of protein which, by electrophoretic and immunochemical properties, appeared identical with transferase 7-7. This enzyme is not detectable in normal hepatocytes. Treatment of rats with trans-stilbene oxide induced the expression of transferase 7-7 in the livers of normal rats as well as in hepatoma-cell-bearing animals. In addition, a 2-fold induction of transferase 7-7 was measured in the hepatoma ascites cells. No significant elevation of any other enzyme forms in the hepatoma cells was noted.
对作为腹水肿瘤生长于大鼠腹腔内的肝癌细胞的胞质谷胱甘肽转移酶含量进行了分析。与正常肝组织相比,肝癌细胞中以Pi类谷胱甘肽转移酶7-7为主。所有主要的肝酶形式均下调至几乎无法检测到的浓度。携带腹水肝癌细胞的大鼠肝脏表达的蛋白量虽低但显著,从电泳和免疫化学特性来看,这些蛋白与转移酶7-7相同。这种酶在正常肝细胞中无法检测到。用反式氧化茋处理大鼠可诱导正常大鼠肝脏以及携带肝癌细胞的动物肝脏中转移酶7-7的表达。此外,在肝癌腹水细胞中检测到转移酶7-7有2倍的诱导。未观察到肝癌细胞中任何其他酶形式有显著升高。