Carruthers C, Baumler A, Neilson A, Pressman D
Cancer Res. 1975 Dec;35(12):3798-06.
The location of binding sites for 3'-methyl-p-dimethylaminoazobenzene (3'-Me-DAB) or metabolites on components of rat liver cells and hepatoma cells in tumors induced by this carcinogen was determined at 2 stages during the induction of tumors in rats: (a) in normal liver immediately following the application of a massive dose of the azocarcinogen by intragastric feeding, and (b) in liver and tumor after hepatomas had developed following repeated exposures to the carcinogen by s.c. injections. Bound 3'-Me-DAB or metabolites were detected by the use of rabbit antisera directed against either p-azoazobenzene or p'-azo-p-dimethylaminoazobenzene in an indirect fluorescent antibody technique. Soon after massive intragastric doses of 3'-Me-DAB, the staining observed when the anti-p-azoazobenzene antiserum was used was principally on cytoplasmic components of liver cells with some staining of the intranuclear components. When the second antiserum, anti-p'-azo-p-dimethylaminoazobenzene antiserum, was used, the most intense fluorescent staining was on the nuclear membranes, although there was some cytoplasmic and intranuclear staining as well.
在大鼠肿瘤诱导的两个阶段,确定了3'-甲基 - 对二甲氨基偶氮苯(3'-Me-DAB)或其代谢产物在大鼠肝癌细胞和肝细胞成分上的结合位点位置:(a)在通过胃内灌喂给予大量偶氮致癌物后立即在正常肝脏中;(b)在通过皮下注射反复接触致癌物后肝癌形成后的肝脏和肿瘤中。在间接荧光抗体技术中,使用针对对偶氮苯或对'-偶氮 - 对二甲氨基偶氮苯的兔抗血清检测结合的3'-Me-DAB或其代谢产物。在胃内给予大量3'-Me-DAB后不久,使用抗对偶氮苯抗血清时观察到的染色主要在肝细胞的细胞质成分上,核内成分也有一些染色。当使用第二种抗血清,即抗对'-偶氮 - 对二甲氨基偶氮苯抗血清时,最强的荧光染色在核膜上,尽管也有一些细胞质和核内染色。