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AKT与去泛素化酶:一种双向关系。

AKT and DUBs: a bidirectional relationship.

作者信息

Serratore Valentina, Lucibello Maria, Malanga Donatella, Viglietto Giuseppe, De Marco Carmela

机构信息

Molecular Oncology Laboratory, Department of Experimental and Clinical Medicine, "Magna Graecia" University, 88100, Catanzaro, Italy.

Department of Biomedical Sciences, Institute for Biomedical Research and Innovation, National Research Council of Italy (CNR), 88100, Catanzaro, Italy.

出版信息

Cell Mol Biol Lett. 2025 Jul 7;30(1):77. doi: 10.1186/s11658-025-00753-3.

Abstract

The serine/threonine kinase Akt is crucial for cell physiology and can also contribute to pathology if its activation and regulation is disturbed. This kinase phosphorylates several substrates involved in mechanisms that are altered in human disease. AKT is regulated by several post-translational modifications (PTMs), including ubiquitination/deubiquitination. Ubiquitination can both target AKT to the proteasome and promote its activation. The interplay with the deubiquitination mechanism plays a crucial role in almost all biological activities of AKT. Information on the mechanisms of AKT deubiquitination and its key players has evolved rapidly in recent years along with the development of potential targeting strategies, although many of them are still unclear. Nevertheless, AKT in turn regulates various deubiquitinases (DUBs), suggesting further targeting strategies for human diseases. In this review, we aim to provide an up-to-date overview of the dual relationship between AKT and DUBs with respect to potential translational aim.

摘要

丝氨酸/苏氨酸激酶Akt对细胞生理功能至关重要,但其激活和调节一旦受到干扰也会导致病理状态。该激酶可磷酸化多种参与人类疾病中发生改变的机制的底物。Akt受多种翻译后修饰(PTM)调控,包括泛素化/去泛素化。泛素化既能将Akt靶向蛋白酶体,也能促进其激活。与去泛素化机制的相互作用在Akt的几乎所有生物学活性中都起着关键作用。近年来,随着潜在靶向策略的发展,关于Akt去泛素化机制及其关键作用因子的信息迅速增加,尽管其中许多仍不清楚。然而,Akt反过来又调节各种去泛素化酶(DUB),这为人类疾病提示了进一步的靶向策略。在本综述中,我们旨在就潜在的转化目标,对Akt与DUB之间的双重关系提供最新概述。

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