结直肠癌中的 E3 泛素连接酶和去泛素酶:新的分子见解和治疗机会。

IF 4.6 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Sunny Kumar , Malini Basu , Mrinal K. Ghosh
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引用次数: 0

摘要

结肠直肠癌(CRC)的治疗效果有限,预后令人沮丧,因此一直面临着挑战,这也凸显了对突破性治疗方法的需求。本综述深入探讨了 E3 泛素连接酶和去泛素化酶(DUBs)的关键作用,强调了它们在 CRC 中作为肿瘤抑制和肿瘤发生的关键调控因子的作用。我们强调了 E3 连接酶和 DUBs 对 CRC 生物过程的不同影响及其显著的多功能性。我们仔细研究了它们对重要信号通路的具体影响,尤其是对 Wnt/β-catenin 和 NF-κB 的影响。了解这些调控机制对于揭示 CRC 进展的复杂性至关重要。重要的是,我们探讨了 E3 连接酶和 DUB 作为新型 CRC 治疗靶点尚未开发的潜力,讨论了可能指导更有效治疗策略的各个方面。总之,我们的简明综述阐明了 E3 泛素连接酶和去泛素化酶在 CRC 中的关键作用,为改变 CRC 治疗格局的创新方法提供了启发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

E3 ubiquitin ligases and deubiquitinases in colorectal cancer: Emerging molecular insights and therapeutic opportunities

E3 ubiquitin ligases and deubiquitinases in colorectal cancer: Emerging molecular insights and therapeutic opportunities

Colorectal cancer (CRC) presents ongoing challenges due to limited treatment effectiveness and a discouraging prognosis, underscoring the need for ground-breaking therapeutic approaches. This review delves into the pivotal role of E3 ubiquitin ligases and deubiquitinases (DUBs), underscoring their role as crucial regulators for tumor suppression and oncogenesis in CRC. We spotlight the diverse impact of E3 ligases and DUBs on CRC's biological processes and their remarkable versatility. We closely examine their specific influence on vital signaling pathways, particularly Wnt/β-catenin and NF-κB. Understanding these regulatory mechanisms is crucial for unravelling the complexities of CRC progression. Importantly, we explore the untapped potential of E3 ligases and DUBs as novel CRC treatment targets, discussing aspects that may guide more effective therapeutic strategies. In conclusion, our concise review illuminates the E3 ubiquitin ligases and deubiquitinases pivotal role in CRC, offering insights to inspire innovative approaches for transforming the treatment landscape in CRC.

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来源期刊
CiteScore
10.00
自引率
2.00%
发文量
151
审稿时长
44 days
期刊介绍: BBA Molecular Cell Research focuses on understanding the mechanisms of cellular processes at the molecular level. These include aspects of cellular signaling, signal transduction, cell cycle, apoptosis, intracellular trafficking, secretory and endocytic pathways, biogenesis of cell organelles, cytoskeletal structures, cellular interactions, cell/tissue differentiation and cellular enzymology. Also included are studies at the interface between Cell Biology and Biophysics which apply for example novel imaging methods for characterizing cellular processes.
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