Jackson Stephen P
Department of Zoology, The Gurdon Institute, University of Cambridge, Cambridge, UK.
Biochem Soc Trans. 2009 Jun;37(Pt 3):483-94. doi: 10.1042/BST0370483.
The DNA of all cells is continually under assault from a wide range of DNA-damaging agents. To counter this threat to their genetic integrity, cells possess systems, collectively known as the DDR (DNA-damage response), to detect DNA damage, signal its presence and mediate its repair. In the present article, I provide an overview of the DDR and then describe how work in my laboratory and elsewhere has identified some of the key protein players that mediate cellular responses to the most cytotoxic form of DNA damage: the DNA DSB (double-strand break). I also discuss some of my laboratory's recent work, which has revealed that the way cells respond to DSBs is modulated in a cell-cycle-dependent manner to ensure that the cell uses the DSB repair system that is most suited to its cell-cycle stage. Finally, I explain how our increasing knowledge of the DDR is suggesting new avenues for treating cancer and provide an example of a DDR-inhibitory drug that is showing promise in clinical trials.
所有细胞的DNA不断受到各种DNA损伤剂的攻击。为了应对这种对其遗传完整性的威胁,细胞拥有一些系统,统称为DDR(DNA损伤反应),用于检测DNA损伤、发出损伤信号并介导其修复。在本文中,我将概述DDR,然后描述我实验室及其他地方的研究如何确定了一些关键蛋白质,它们介导细胞对最具细胞毒性的DNA损伤形式——DNA双链断裂(DSB)的反应。我还将讨论我实验室最近的一些工作,这些工作揭示了细胞对DSB的反应方式以细胞周期依赖性方式受到调节,以确保细胞使用最适合其细胞周期阶段的DSB修复系统。最后,我将解释我们对DDR的不断深入了解如何为癌症治疗开辟新途径,并提供一种在临床试验中显示出前景的DDR抑制药物的例子。