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超越激酶:在癌症治疗中靶向复制应激蛋白。

Beyond Kinases: Targeting Replication Stress Proteins in Cancer Therapy.

机构信息

Terry Fox Laboratory, BC Cancer, Vancouver, BC, Canada.

Terry Fox Laboratory, BC Cancer, Vancouver, BC, Canada; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.

出版信息

Trends Cancer. 2021 May;7(5):430-446. doi: 10.1016/j.trecan.2020.10.010. Epub 2020 Nov 14.

Abstract

DNA replication stress describes a state of impaired replication fork progress that triggers a cellular stress response to maintain genome stability and complete DNA synthesis. Replication stress is a common state that must be tolerated in many cancers. One promising therapeutic approach is targeting replication stress response factors such as the ataxia telangiectasia and rad 3-related kinase (ATR) or checkpoint kinase 1 (CHK1) kinases that some cancers depend upon to survive endogenous replication stress. However, research revealing the complexity of the replication stress response suggests new genetic interactions and candidate therapeutic targets. Many of these candidates regulate DNA transactions around reversed replication forks, including helicases, nucleases and alternative polymerases that promote fork stability and restart. Here we review emerging strategies to exploit replication stress for cancer therapy.

摘要

DNA 复制压力描述了一种复制叉进展受损的状态,会触发细胞应激反应以维持基因组稳定性并完成 DNA 合成。复制压力是许多癌症中必须耐受的常见状态。一种有前途的治疗方法是针对复制压力反应因子,如共济失调毛细血管扩张症和 rad 3 相关激酶 (ATR) 或检查点激酶 1 (CHK1) 激酶,一些癌症依赖这些因子来存活于内源性复制压力。然而,揭示复制压力反应复杂性的研究表明存在新的遗传相互作用和候选治疗靶点。其中许多候选物调节逆转复制叉周围的 DNA 交易,包括解旋酶、核酸酶和促进叉稳定性和重启动的替代聚合酶。在这里,我们综述了利用复制压力进行癌症治疗的新兴策略。

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