Lubet R A, McCarvill J T, Putman D L, Schwartz J L, Schechtman L M
Carcinogenesis. 1984 Apr;5(4):459-62. doi: 10.1093/carcin/5.4.459.
3-Aminobenzamide, a potent inhibitor of nuclear poly ADP-ribosyl synthetase, was tested for its ability to alter the toxic and/or transforming effects of ethyl methanesulfonate, methyl methanesulfonate and 3-methylcholanthrene in BALB/3T3 clone A31-1 cells. 3-Aminobenzamide enhanced the toxic effects of both ethyl methanesulfonate and methyl methanesulfonate in a dose dependent manner, but had minimal effects on 3-methylcholanthrene induced toxicity. Similarly, 3-aminobenzamide greatly enhanced ethyl methanesulfonate induced transformation while failing to enhance the transformation of BALB/3T3 clone A31-1 cells by 3-methylcholanthrene. These results stress the importance of poly ADP-ribosyl synthetase in repair of DNA damage and the chemical induction of transformation in vitro.
3-氨基苯甲酰胺是一种有效的核多聚ADP-核糖基合成酶抑制剂,测试了其改变甲磺酸乙酯、甲磺酸甲酯和3-甲基胆蒽对BALB/3T3克隆A31-1细胞的毒性和/或转化作用的能力。3-氨基苯甲酰胺以剂量依赖性方式增强了甲磺酸乙酯和甲磺酸甲酯的毒性作用,但对3-甲基胆蒽诱导的毒性影响极小。同样,3-氨基苯甲酰胺极大地增强了甲磺酸乙酯诱导的转化作用,而未能增强3-甲基胆蒽对BALB/3T3克隆A31-1细胞的转化作用。这些结果强调了多聚ADP-核糖基合成酶在DNA损伤修复和体外化学诱导转化中的重要性。