Beyersmann D
Department of Biology and Chemistry, University of Bremen, Germany.
Toxicol Lett. 1994 Jun;72(1-3):333-8. doi: 10.1016/0378-4274(94)90045-0.
The carcinogenicity and genotoxicity of cadmium, chromium, cobalt and nickel strongly depend on their chemical ligands (speciation) which modulate their bioavailability and reactivity with biochemical targets. With the exception of hexavalent chromium, carcinogenic metal compounds are only weakly genotoxic. However, the ions of the carcinogenic metals cadmium, cobalt and nickel, and also the noncarcinogenic lead, inhibit the repair of DNA damaged by direct genotoxic agents like UV irradiation and alkylating substances, thereby enhancing the effects of the latter agents. These effects are interpreted by the interference of the toxic metal ions with biochemical functions of magnesium, calcium and zinc ions.
镉、铬、钴和镍的致癌性和遗传毒性在很大程度上取决于它们的化学配体(形态),这些配体调节它们的生物利用度以及与生化靶点的反应活性。除六价铬外,致癌金属化合物的遗传毒性较弱。然而,致癌金属镉、钴和镍的离子,以及非致癌的铅离子,会抑制由紫外线照射和烷基化物质等直接遗传毒性剂造成的DNA损伤的修复,从而增强后一类物质的作用。这些效应被解释为有毒金属离子对镁、钙和锌离子生化功能的干扰。