Department of Oncology, Mayo Clinic, Rochester, Minnesota, USA.
Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, Minnesota, USA.
Environ Mol Mutagen. 2020 Aug;61(7):716-729. doi: 10.1002/em.22381. Epub 2020 Jul 9.
Many environmental carcinogens cause DNA damage, which can result in mutations and other alterations in genomic DNA if not repaired promptly. Because of the bulkiness of the lesions, DNA-protein crosslinks (DPCs) are one of the types of toxic DNA damage with potentially deleterious consequences. Despite the importance of DPCs, how cells remove these complex DNA adducts has been incompletely understood. However, major progress in the DPC repair field over the past 5 years now supports the view that cells are equipped with multiple mechanisms to cope with DPCs. Here, we first provide an overview of environmental substances that induce DPCs, describing the sources of exposure and mechanisms of DPC formation. We then review current models of DPC repair and discuss their significance for environmental carcinogens.
许多环境致癌物会导致 DNA 损伤,如果不能及时修复,就会导致基因突变和其他基因组 DNA 改变。由于损伤的体积较大,DNA-蛋白质交联(DPC)是一种具有潜在有害后果的毒性 DNA 损伤类型。尽管 DPC 很重要,但细胞如何去除这些复杂的 DNA 加合物尚未完全了解。然而,过去 5 年来 DPC 修复领域的重大进展现在支持这样一种观点,即细胞配备了多种机制来应对 DPC。在这里,我们首先概述了诱导 DPC 的环境物质,描述了暴露源和 DPC 形成的机制。然后,我们回顾了 DPC 修复的现行模型,并讨论了它们对环境致癌物的意义。