Newcastle Centre for Cancer Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.
Wolfson Childhood Cancer Research Centre, Newcastle Centre for Cancer, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, NE1 7RU, UK.
Expert Rev Mol Med. 2020 Jun 8;22:e2. doi: 10.1017/erm.2020.3.
DNA damage response (DDR) pathway prevents high level endogenous and environmental DNA damage being replicated and passed on to the next generation of cells via an orchestrated and integrated network of cell cycle checkpoint signalling and DNA repair pathways. Depending on the type of damage, and where in the cell cycle it occurs different pathways are involved, with the ATM-CHK2-p53 pathway controlling the G1 checkpoint or ATR-CHK1-Wee1 pathway controlling the S and G2/M checkpoints. Loss of G1 checkpoint control is common in cancer through TP53, ATM mutations, Rb loss or cyclin E overexpression, providing a stronger rationale for targeting the S/G2 checkpoints. This review will focus on the ATM-CHK2-p53-p21 pathway and the ATR-CHK1-WEE1 pathway and ongoing efforts to target these pathways for patient benefit.
DNA 损伤反应 (DDR) 途径通过细胞周期检查点信号和 DNA 修复途径的协调和综合网络,防止高水平的内源性和环境 DNA 损伤被复制并传递到下一代细胞。根据损伤的类型和发生的细胞周期位置,涉及不同的途径,ATM-CHK2-p53 途径控制 G1 检查点,ATR-CHK1-Wee1 途径控制 S 和 G2/M 检查点。通过 TP53、ATM 突变、Rb 缺失或细胞周期蛋白 E 过表达,G1 检查点控制在癌症中常见,这为靶向 S/G2 检查点提供了更强的理由。这篇综述将重点介绍 ATM-CHK2-p53-p21 途径和 ATR-CHK1-WEE1 途径,以及为了患者获益而针对这些途径的正在进行的努力。