Department of Medical Oncology, Dr BRAIRCH, All India Institute of Medical Sciences, New Delhi 110029, India.
School of Biotechnology, Shri Mata Vaishno Devi University, Katra, Jammu and Kashmir 182320, India.
Biochim Biophys Acta Gene Regul Mech. 2023 Dec;1866(4):194979. doi: 10.1016/j.bbagrm.2023.194979. Epub 2023 Aug 24.
The ubiquitin proteasomal system (UPS) represents a highly regulated protein degradation pathway essential for maintaining cellular homeostasis. This system plays a critical role in several cellular processes, which include DNA damage repair, cell cycle checkpoint control, and immune response regulation. Recently, the UPS has emerged as a promising target for cancer therapeutics due to its involvement in oncogenesis and tumor progression. Here we aim to summarize the key aspects of the UPS and its significance in cancer therapeutics. We begin by elucidating the fundamental components of the UPS, highlighting the role of ubiquitin, E1-E3 ligases, and the proteasome in protein degradation. Furthermore, we discuss the intricate process of ubiquitination and proteasomal degradation, emphasizing the specificity and selectivity achieved through various signaling pathways. The dysregulation of the UPS has been implicated in cancer development and progression. Aberrant ubiquitin-mediated degradation of key regulatory proteins, such as tumor suppressors and oncoproteins, can lead to uncontrolled cell proliferation, evasion of apoptosis, and metastasis. We outline the pivotal role of the UPS in modulating crucial oncogenic pathways, including the regulation of cyclins, transcription factors, Replication stress components and DNA damage response. The increasing recognition of the UPS as a target for cancer therapeutics has spurred the development of small molecules, peptides, and proteasome inhibitors with the potential to restore cellular balance and disrupt tumor growth. We provide an overview of current therapeutic strategies aimed at exploiting the UPS, including the use of proteasome inhibitors, deubiquitinating enzyme inhibitors, and novel E3 ligase modulators. We further discuss novel emerging strategies for the development of next-generation drugs that target proteasome inhibitors. Exploiting the UPS for cancer therapeutics offers promising avenues for developing innovative and effective treatment strategies, providing hope for improved patient outcomes in the fight against cancer.
泛素蛋白酶体系统 (UPS) 是一种高度调控的蛋白质降解途径,对维持细胞内稳态至关重要。该系统在多种细胞过程中发挥着关键作用,包括 DNA 损伤修复、细胞周期检查点控制和免疫反应调节。最近,UPS 作为癌症治疗的一个有前途的靶点出现,因为它参与了肿瘤发生和肿瘤进展。在这里,我们旨在总结 UPS 的关键方面及其在癌症治疗中的意义。我们首先阐明 UPS 的基本组成部分,强调泛素、E1-E3 连接酶和蛋白酶体在蛋白质降解中的作用。此外,我们讨论了泛素化和蛋白酶体降解的复杂过程,强调了通过各种信号通路实现的特异性和选择性。UPS 的失调与癌症的发展和进展有关。异常的泛素介导的关键调节蛋白的降解,如肿瘤抑制因子和癌蛋白,可以导致不受控制的细胞增殖、逃避细胞凋亡和转移。我们概述了 UPS 在调节关键致癌途径中的关键作用,包括调节细胞周期蛋白、转录因子、复制应激成分和 DNA 损伤反应。UPS 作为癌症治疗靶点的日益认识,促使开发了具有恢复细胞平衡和破坏肿瘤生长潜力的小分子、肽和蛋白酶体抑制剂。我们提供了目前旨在利用 UPS 的治疗策略概述,包括使用蛋白酶体抑制剂、去泛素化酶抑制剂和新型 E3 连接酶调节剂。我们进一步讨论了开发靶向蛋白酶体抑制剂的下一代药物的新出现的策略。利用 UPS 进行癌症治疗为开发创新和有效的治疗策略提供了有希望的途径,为改善癌症治疗中的患者预后带来了希望。