Faletto M B, Koser P L, Battula N, Townsend G K, Maccubbin A E, Gelboin H V, Gurtoo H L
Department of Experimental Therapeutics, Grace Cancer Drug Center, Roswell Park Memorial Institute, Buffalo, New York 14263.
J Biol Chem. 1988 Sep 5;263(25):12187-9.
Aflatoxin B1 (AFB1), a potent hepatocarcinogen and ubiquitous dietary contaminant in some countries, is detoxified to aflatoxin M1 (AFM1) via cytochrome P-450-mediated AFB1-4-hydroxylase. Genetic studies in mice have demonstrated that the expression of AFB1-4-hydroxylase is regulated by the aryl hydrocarbon locus and suggested that different cytochrome P-450 isozymes catalyze AFB1-4-hydroxylase and aryl hydrocarbon hydroxylase activities. We have now examined lysates from mammalian cells infected with recombinant vaccinia viruses containing expressible cytochrome P1-450 or P3-450 cDNAs for their ability to metabolize AFB1 to AFM1. Our results show that cytochrome P3-450 cDNA specifies AFB1-4-hydroxylase. This is the first direct assignment of a specific cytochrome P-450 to an AFB1 detoxification pathway. This finding may have relevance to the dietary modulation of AFB1 hepatocarcinogenesis.
黄曲霉毒素B1(AFB1)是一种强效的肝癌致癌物,在一些国家是普遍存在的饮食污染物,它通过细胞色素P - 450介导的AFB1 - 4 - 羟化酶被解毒为黄曲霉毒素M1(AFM1)。对小鼠的遗传学研究表明,AFB1 - 4 - 羟化酶的表达受芳烃位点调控,并提示不同的细胞色素P - 450同工酶催化AFB1 - 4 - 羟化酶和芳烃羟化酶活性。我们现在检测了感染含有可表达细胞色素P1 - 450或P3 - 450 cDNA的重组痘苗病毒的哺乳动物细胞裂解物将AFB1代谢为AFM1的能力。我们的结果表明,细胞色素P3 - 450 cDNA确定了AFB1 - 4 - 羟化酶。这是首次将特定的细胞色素P - 450直接确定为AFB1解毒途径。这一发现可能与AFB1肝癌发生的饮食调节有关。