Lan Huiyin, Sun Yi
Department of Thoracic Radiation Oncology, Zhejiang Cancer Hospital, Cancer Hospital of University of Chinese Academy of Sciences, Hangzhou, China.
Institute of Cancer and Basic Medicine, Chinese Academy of Sciences, Hangzhou, China.
Front Cell Dev Biol. 2021 Oct 25;9:751574. doi: 10.3389/fcell.2021.751574. eCollection 2021.
The proper DNA damage response (DDR) and repair are the central molecular mechanisms for the maintenance of cellular homeostasis and genomic integrity. The abnormality in this process is frequently observed in human cancers, and is an important contributing factor to cancer development. FBXW7 is an F-box protein serving as the substrate recognition component of SCF (SKP1-CUL1-F-box protein) E3 ubiquitin ligase. By selectively targeting many oncoproteins for proteasome-mediated degradation, FBXW7 acts as a typical tumor suppressor. Recent studies have demonstrated that FBXW7 also plays critical roles in the process of DDR and repair. In this review, we first briefly introduce the processes of protein ubiquitylation by SCF and DDR/repair, then provide an overview of the molecular characteristics of FBXW7. We next discuss how FBXW7 regulates the process of DDR and repair, and its translational implication. Finally, we propose few future perspectives to further elucidate the role of FBXW7 in regulation of a variety of biological processes and tumorigenesis, and to design a number of approaches for FBXW7 reactivation in a subset of human cancers for potential anticancer therapy.
适当的DNA损伤反应(DDR)和修复是维持细胞内稳态和基因组完整性的核心分子机制。在人类癌症中经常观察到这一过程的异常,并且是癌症发展的一个重要促成因素。FBXW7是一种F-box蛋白,作为SCF(SKP1-CUL1-F-box蛋白)E3泛素连接酶的底物识别成分。通过选择性地将许多癌蛋白靶向蛋白酶体介导的降解,FBXW7作为一种典型的肿瘤抑制因子发挥作用。最近的研究表明,FBXW7在DDR和修复过程中也起着关键作用。在这篇综述中,我们首先简要介绍SCF介导的蛋白质泛素化过程以及DDR/修复过程,然后概述FBXW7的分子特征。接下来,我们讨论FBXW7如何调节DDR和修复过程及其转化意义。最后,我们提出了一些未来的展望,以进一步阐明FBXW7在调节多种生物学过程和肿瘤发生中的作用,并设计一些方法来重新激活一部分人类癌症中的FBXW7,用于潜在的抗癌治疗。