Allaudeen H S, Snyder R M, Whitman M H, Crooke S T
Biochem Pharmacol. 1985 Sep 15;34(18):3243-50. doi: 10.1016/0006-2952(85)90341-7.
Auranofin, a coordinated gold compound, inhibits in vitro DNA synthesis and displays in vivo antitumor activity. To understand the mechanisms of inhibition of DNA replication, we have examined the effects of auranofin and other gold complexes on the activities of purified cellular and herpesvirus-induced DNA polymerases, and on in situ DNA replication in permeabilized S phase KB cells. Evaluation of the data suggests the following conclusions. (1) The gold compounds varied in their abilities to inhibit DNA polymerase activities. DNA polymerase alpha was more sensitive to inhibition by gold compounds than DNA polymerase beta; (2) Inhibition of purified DNA polymerases by gold (I) compounds was noncompetitive with both DNA template and triphosphate substrates. Inhibition by SKF 101675, a gold (III) complex was competitive with DNA. (3) None of the gold compounds tested preferentially inhibited herpesvirus-induced DNA polymerases. (4) The gold complexes that inhibited in vitro DNA replication also inhibited in situ DNA synthesis. However, the potency and order of potency of the compounds varied between the in vitro and in situ systems. (5) Auranofin and other gold compounds inhibited the clonogenic capacity of KB cells in a concentration-dependent manner. The IC50 values measured in the clonogenic assay were significantly lower than those obtained from the in vitro and in situ DNA replication assays.
金诺芬是一种配位金化合物,它能在体外抑制DNA合成,并在体内显示出抗肿瘤活性。为了了解抑制DNA复制的机制,我们研究了金诺芬和其他金配合物对纯化的细胞及疱疹病毒诱导的DNA聚合酶活性的影响,以及对通透化的S期KB细胞原位DNA复制的影响。对数据的评估得出以下结论:(1)金化合物抑制DNA聚合酶活性的能力各不相同。DNA聚合酶α比DNA聚合酶β对金化合物的抑制更敏感;(2)金(I)化合物对纯化的DNA聚合酶的抑制作用对DNA模板和三磷酸底物均无竞争性。金(III)配合物SKF 101675的抑制作用与DNA具有竞争性。(3)所测试的金化合物均未优先抑制疱疹病毒诱导的DNA聚合酶。(4)抑制体外DNA复制的金配合物也抑制原位DNA合成。然而,化合物在体外和原位系统中的效力和效力顺序有所不同。(5)金诺芬和其他金化合物以浓度依赖的方式抑制KB细胞的克隆形成能力。克隆形成试验中测得的IC50值显著低于体外和原位DNA复制试验中获得的值。