Chen Shuyi, Li Ling
The Sixth Student Battalion, School of Basic Medical Sciences, Fourth Military Medical University, Xi'an, China.
Department of Cell Biology, National Translational Science Center for Molecular Medicine, Fourth Military Medical University, Xi'an, China.
Front Oncol. 2022 Aug 18;12:949688. doi: 10.3389/fonc.2022.949688. eCollection 2022.
Cyclin D1 has been reported to be upregulated in several solid and hematologic tumors, promoting cancer progression. Thus, decreasing cyclin D1 by degradation could be a promising target strategy for cancer therapy. This mini review summarizes the roles of cyclin D1 in tumorigenesis and progression and its degradation strategies. Besides, we proposed an exploration of the degradation of cyclin D1 by FBX4, an F box protein belonging to the E3 ligase SKP-CUL-F-box (SCF) complex, which mediates substrate ubiquitination, as well as a postulate about the concrete combination mode of FBX4 and cyclin D1. Furthermore, we proposed a possible photodynamic therapy strategythat is based on the above concrete combination mode for treating superficial cancer.
据报道,细胞周期蛋白D1在多种实体瘤和血液系统肿瘤中表达上调,促进癌症进展。因此,通过降解来降低细胞周期蛋白D1可能是一种有前景的癌症治疗靶向策略。本综述总结了细胞周期蛋白D1在肿瘤发生和进展中的作用及其降解策略。此外,我们提出探索由FBX4介导的细胞周期蛋白D1的降解,FBX4是一种属于E3连接酶SKP-CUL-F-box(SCF)复合物的F盒蛋白,可介导底物泛素化,同时还提出了关于FBX4与细胞周期蛋白D1具体结合模式的假设。此外,我们基于上述具体结合模式提出了一种可能的光动力治疗浅表癌的策略。