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WEE1 激酶限制 CDK 活性以保护 DNA 复制和有丝分裂进入。

WEE1 kinase limits CDK activities to safeguard DNA replication and mitotic entry.

机构信息

Biotech Research and Innovation Centre, University of Copenhagen, Ole Maaløes Vej 5, Copenhagen 2200 N, Denmark.

Biotech Research and Innovation Centre, University of Copenhagen, Ole Maaløes Vej 5, Copenhagen 2200 N, Denmark.

出版信息

Mutat Res. 2020 Jan-Apr;819-820:111694. doi: 10.1016/j.mrfmmm.2020.111694. Epub 2020 Feb 25.

Abstract

Precise execution of the cell division cycle is vital for all organisms. The Cyclin dependent kinases (CDKs) are the main cell cycle drivers, however, their activities must be precisely fine-tuned to ensure orderly cell cycle progression. A major regulatory axis is guarded by WEE1 kinase, which directly phosphorylates and inhibits CDK1 and CDK2. The role of WEE1 in the G2/M cell-cycle phase has been thoroughly investigated, and it is a focal point of multiple clinical trials targeting a variety of cancers in combination with DNA-damaging chemotherapeutic agents. However, the emerging role of WEE1 in S phase has so far largely been neglected. Here, we review how WEE1 regulates cell-cycle progression highlighting the importance of this kinase for proper S phase. We discuss how its function is modulated throughout different cell-cycle stages and provide an overview of how WEE1 levels are regulated. Furthermore, we outline recent clinical trials targeting WEE1 and elaborate on the mechanisms behind the anticancer efficacy of WEE1 inhibition. Finally, we consider novel biomarkers that may benefit WEE1-inhibition approaches in the clinic.

摘要

精确执行细胞分裂周期对所有生物体都是至关重要的。细胞周期蛋白依赖性激酶(CDKs)是细胞周期的主要驱动因素,然而,它们的活性必须被精确地微调,以确保细胞周期的有序进行。WEE1 激酶是一个主要的调节轴,它直接磷酸化并抑制 CDK1 和 CDK2。WEE1 在 G2/M 细胞周期阶段的作用已经被彻底研究过,它是多种针对各种癌症的临床试验的焦点,与 DNA 损伤化疗药物联合使用。然而,WEE1 在 S 期的新兴作用迄今为止在很大程度上被忽视了。在这里,我们回顾了 WEE1 如何调节细胞周期进程,强调了这种激酶对适当的 S 期的重要性。我们讨论了其功能在不同的细胞周期阶段是如何被调节的,并概述了 WEE1 水平的调节方式。此外,我们还概述了针对 WEE1 的最近临床试验,并详细阐述了 WEE1 抑制的抗癌疗效背后的机制。最后,我们考虑了可能有益于临床中 WEE1 抑制方法的新型生物标志物。

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