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靶向衰老过程中的DNA损伤:实现DNA修复的强化

Targeting DNA damage in ageing: towards supercharging DNA repair.

作者信息

Bujarrabal-Dueso Arturo, Garinis George A, Robbins Paul D, Vijg Jan, Schumacher Björn

机构信息

Institute for Genome Stability in Aging and Disease, University and University Hospital of Cologne, Cologne, Germany.

Cologne Excellence Cluster for Cellular Stress Responses in Ageing-Associated Diseases (CECAD), Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany.

出版信息

Nat Rev Drug Discov. 2025 Jun 12. doi: 10.1038/s41573-025-01212-6.

Abstract

Ageing is the most important risk factor for many common human diseases, including cancer, diabetes, neurodegeneration and cardiovascular disease. Consequently, combating ageing itself has emerged as a rational strategy for addressing age-related multimorbidity. Over the past three decades, multiple genetic and pharmacologic interventions have led to substantial extension of lifespan and healthspan in model organisms. However, it is unclear whether these interventions target the causal mechanisms of ageing or downstream consequences. Ample evidence suggests that DNA damage to the somatic genome is a major causal mechanism of ageing, which compromises essential cellular functions such as transcription and replication, and leads to cellular senescence, apoptosis and mutations. Recently, new concepts have emerged to target the main consequences of DNA damage and enhance DNA repair capacities, thereby extending maintenance of the genome. Here, we review advances in this field and discuss approaches to pharmacologically mitigate the adverse effects of DNA damage to delay ageing, prevent mutation-driven cancer and mitigate age-related degenerative diseases.

摘要

衰老是许多常见人类疾病的最重要风险因素,包括癌症、糖尿病、神经退行性疾病和心血管疾病。因此,对抗衰老本身已成为解决与年龄相关的多种疾病的合理策略。在过去三十年中,多种基因和药物干预已使模式生物的寿命和健康寿命大幅延长。然而,尚不清楚这些干预措施是针对衰老的因果机制还是下游后果。大量证据表明,体细胞基因组的DNA损伤是衰老的主要因果机制,它会损害转录和复制等基本细胞功能,并导致细胞衰老、凋亡和突变。最近,出现了一些新的概念,旨在针对DNA损伤的主要后果并增强DNA修复能力,从而延长基因组的维持时间。在这里,我们综述该领域的进展,并讨论通过药理学方法减轻DNA损伤的不利影响以延缓衰老、预防突变驱动的癌症和减轻与年龄相关的退行性疾病的方法。

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