Kim Ahhyun, Benavente Claudia A
Department of Pharmaceutical Sciences, University of California, Irvine, CA 92697, USA.
Department of Developmental and Cell Biology, University of California, Irvine, CA 92697, USA.
Epigenomes. 2024 Jul 1;8(3):26. doi: 10.3390/epigenomes8030026.
Ubiquitin-like with PHD and RING finger domains 1 (UHRF1) is an essential protein involved in the maintenance of repressive epigenetic marks, ensuring epigenetic stability and fidelity. As an epigenetic regulator, UHRF1 comprises several functional domains (UBL, TTD, PHD, SRA, RING) that are collectively responsible for processes like DNA methylation, histone modification, and DNA repair. UHRF1 is a downstream effector of the RB/E2F pathway, which is nearly universally deregulated in cancer. Under physiological conditions, UHRF1 protein levels are cell cycle-dependent and are post-translationally regulated by proteasomal degradation. Conversely, UHRF1 is overexpressed and serves as an oncogenic driver in multiple cancers. This review focuses on the functional domains of UHRF1, highlighting its key interacting proteins and oncogenic roles in solid tumors including retinoblastoma, osteosarcoma, lung cancer, and breast cancer. Additionally, current therapeutic strategies targeting UHRF1 domains or its interactors are explored, providing an insight on potential clinical applications.
含PHD和RING结构域的类泛素蛋白1(UHRF1)是一种重要蛋白质,参与维持抑制性表观遗传标记,确保表观遗传稳定性和忠实性。作为一种表观遗传调节因子,UHRF1包含几个功能结构域(UBL、TTD、PHD、SRA、RING),它们共同负责DNA甲基化、组蛋白修饰和DNA修复等过程。UHRF1是RB/E2F通路的下游效应因子,该通路在癌症中几乎普遍失调。在生理条件下,UHRF1蛋白水平依赖细胞周期,并通过蛋白酶体降解进行翻译后调控。相反,UHRF1在多种癌症中过表达并充当致癌驱动因子。本综述重点关注UHRF1的功能结构域,突出其在实体瘤(包括视网膜母细胞瘤、骨肉瘤、肺癌和乳腺癌)中的关键相互作用蛋白和致癌作用。此外,还探讨了目前针对UHRF1结构域或其相互作用分子的治疗策略,为潜在的临床应用提供见解。