Kozhemiakina O V, Iaguzhinskiĭ L S
Biokhimiia. 1993 Aug;58(8):1176-87.
Literary data concerning structure-activity relationships in compounds exhibiting an antipromoter activity in skin tests of full tumour promotion by 12-O-tetradecanoyl-phorbol-13-acetate (TPA) or its analogs have been reviewed. Five classes of antipromoters differing in their action on the first and second stages of tumour promotion have been identified, namely: i) 2nd stage promoters/1st stage inhibitors; ii) 1st stage promoters/2nd stage inhibitors; iii) 2nd stage inhibitors; iiii) 1st stage inhibitors; iiiii) 1st and 2nd stage inhibitors. The results on structure-activity of antipromoters were compared with the results of previous studies on phorbol tumour promoters. These data made it possible to determine the reciprocal localization of binding sites for various classes of antipromoters and individual functionally important phorbol fragments on protein kinase C. A new detailed variant of the model of two-center binding of full phorbol tumour promoters on protein kinase C is proposed.
有关在12-O-十四烷酰佛波醇-13-乙酸酯(TPA)或其类似物的完全肿瘤促进皮肤试验中表现出抗启动子活性的化合物结构-活性关系的文献数据已被综述。已鉴定出五类在肿瘤促进的第一阶段和第二阶段作用不同的抗启动子,即:i)第二阶段启动子/第一阶段抑制剂;ii)第一阶段启动子/第二阶段抑制剂;iii)第二阶段抑制剂;iiii)第一阶段抑制剂;iiiii)第一阶段和第二阶段抑制剂。将抗启动子的结构-活性结果与先前关于佛波醇肿瘤启动子的研究结果进行了比较。这些数据使得确定各类抗启动子和蛋白质激酶C上各个功能重要的佛波醇片段的结合位点的相互定位成为可能。提出了全佛波醇肿瘤启动子在蛋白质激酶C上双中心结合模型的一个新的详细变体。