创新链/学科链/研发链/产业链

新药研发前沿动态 / 医药领域趋势进展

Wee1激酶及其抑制剂研究进展

Research Progress of Wee1 Kinase and Its Inhibitors

  • 摘要: 有丝分裂是在细胞周期的精准调控下完成的。细胞周期依靠G1/S期检查点、S期检查点和G2/M期检查点及时阻滞分裂进程,确保遗传信息的完整性。由于多数人类肿瘤细胞存在由于p53突变、p53功能缺陷导致G1/S期检查点失活,从而更依赖于G2/M检查点的调控。细胞周期调节蛋白Wee1激酶是G2/M检查点的关键调控因子,通过磷酸化周期蛋白依赖性激酶1(CDK1)的第15位酪氨酸实现G2/M期阻滞,为DNA修复提供了时间。抑制Wee1可消除细胞周期阻滞,使肿瘤细胞过早进入有丝分裂,产生复制应激和有丝分裂灾难,且Wee1在许多肿瘤中高表达,因此是一个治疗肿瘤的理想靶点,目前其抑制剂已成为研究热门。通过对Wee1激酶的作用机制、与疾病的相关性和在研小分子抑制剂的临床应用进行详细介绍,为其进一步研究和应用提供参考。

     

    Abstract: Mitosis is completed under the precise control of cell cycle, which relies on the checkpoints of G1/S phase, S phase and G2/M phase to block the division process in time to ensure the integrity of genetic information. Since most human tumor cells have p53 mutations and p53 functional defects, the G1/S phase checkpoints are inactivated, leading to higher dependence on the regulation of G2/M checkpoints. The cell cycle regulatory protein Wee1 kinase is a key regulator of the G2/M checkpoint. It achieves G2/M phase blocked by phosphorylation of CDK1 Tyr15, which provides time for DNA repair. Inhibition of Wee1 can eliminate cell cycle block, make tumor cells enter mitosis prematurely, and produce replication stress and mitotic disaster. Wee1 is highly expressed in many tumors, so it is an ideal target for the treatment of tumors, with its inhibitors becoming a hot research topic. This article mainly introduces the mechanism of Wee1 kinase, its relevance to diseases, and the clinical application of small molecule inhibitors under investigation, in order to provide ideas for its further research and application.

     

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