Williams Dean T, Staples Christopher J
School of Medical Sciences, Bangor University, Bangor, Gwynedd, LL57 2DG, UK.
Department of Vascular Surgery, Ysbyty Gwynedd, Bangor, LL57 2PW, UK.
Adv Exp Med Biol. 2017;1007:1-16. doi: 10.1007/978-3-319-60733-7_1.
Genome stability is maintained by a number of elegant mechanisms, which sense and repair damaged DNA. Germline defects that compromise genomic integrity result in cancer predisposition, exemplified by rare syndromes caused by mutations in certain DNA repair genes. These individuals often exhibit other symptoms including progeria and neurodegeneration. Paradoxically, some of these deleterious genetic alterations provide novel therapeutic opportunities to target cancer cells; an excellent example of such an approach being the recent development of poly (ADP-ribose) polymerase inhibitors as the first 'synthetic lethal' medicine for patients with BRCA-mutant cancers. The therapeutic exploitation of synthetic lethal interactions has enabled a novel approach to personalised medicine based on continued molecular profiling of patient and tumour material. This profiling may also aid clinicians in the identification of specific drug resistance mechanisms following relapse, and enable appropriate modification of the therapeutic regimen. This chapter focuses on therapeutic strategies designed to target aspects of the DNA damage response, and examines emerging themes demonstrating mechanistic overlap between DNA repair and neurodegeneration.
基因组稳定性由多种精妙机制维持,这些机制可感知并修复受损DNA。损害基因组完整性的生殖系缺陷会导致癌症易感性,某些DNA修复基因突变引起的罕见综合征就是例证。这些个体常表现出早衰和神经退行性变等其他症状。矛盾的是,其中一些有害的基因改变为靶向癌细胞提供了新的治疗机会;聚(ADP - 核糖)聚合酶抑制剂作为治疗携带BRCA突变癌症患者的首款“合成致死”药物的最新进展就是这种方法的一个绝佳例子。对合成致死相互作用的治疗性利用为基于对患者和肿瘤材料持续进行分子分析的个性化医疗开辟了一条新途径。这种分析还可帮助临床医生在复发后识别特定的耐药机制,并对治疗方案进行适当调整。本章重点介绍旨在针对DNA损伤反应各方面的治疗策略,并探讨显示DNA修复与神经退行性变之间存在机制重叠的新主题。