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NEDD4 相关 HECT 型 E3 泛素连接酶在癌细胞中缺陷自噬中的作用:分子机制和治疗前景。

The role of NEDD4 related HECT-type E3 ubiquitin ligases in defective autophagy in cancer cells: molecular mechanisms and therapeutic perspectives.

机构信息

Department of Thoracic Surgery, The Seventh People's Hospital of Chengdu, Chengdu, 610021, Sichuan, People's Republic of China.

Scientific Research Laboratory Center, First Affiliated Hospital of Kunming Medical University, Kunming, 650032, Yunnan, People's Republic of China.

出版信息

Mol Med. 2023 Mar 14;29(1):34. doi: 10.1186/s10020-023-00628-3.

Abstract

The homologous to the E6-AP carboxyl terminus (HECT)-type E3 ubiquitin ligases are the selective executers in the protein ubiquitination, playing a vital role in modulation of the protein function and stability. Evidence shows the regulatory role of HECT-type E3 ligases in various steps of the autophagic process. Autophagy is an intracellular digestive and recycling process that controls the cellular hemostasis. Defective autophagy is involved in tumorigenesis and has been detected in various types of cancer cells. A growing body of findings indicates that HECT-type E3 ligases, in particular members of the neural precursor cell expressed developmentally downregulated protein 4 (NEDD4) including NEDD4-1, NEDD4-L, SMURFs, WWPs, and ITCH, play critical roles in dysregulation or dysfunction of autophagy in cancer cells. The present review focuses on NEDD4 E3 ligases involved in defective autophagy in cancer cells and discusses their autophagic function in different cancer cells as well as substrates and the signaling pathways in which they participate, conferring a basis for the cancer treatment through the modulating of these E3 ligases.

摘要

同源物到 E6-AP 羧基末端 (HECT)-型 E3 泛素连接酶是蛋白质泛素化的选择性执行者,在调节蛋白质功能和稳定性方面发挥着重要作用。有证据表明 HECT 型 E3 连接酶在自噬过程的各个步骤中具有调节作用。自噬是一种细胞内消化和再循环过程,可控制细胞止血。自噬功能缺陷与肿瘤发生有关,并在各种类型的癌细胞中检测到。越来越多的研究结果表明,HECT 型 E3 连接酶,特别是神经前体细胞表达发育下调蛋白 4(NEDD4)的成员,包括 NEDD4-1、NEDD4-L、SMURFs、WWPs 和 ITCH,在癌细胞中自噬的失调或功能障碍中发挥关键作用。本综述重点介绍了参与癌细胞中缺陷自噬的 NEDD4 E3 连接酶,并讨论了它们在不同癌细胞中的自噬功能以及它们参与的底物和信号通路,为通过调节这些 E3 连接酶进行癌症治疗提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4078/10015828/dfa0bd8e4247/10020_2023_628_Fig1_HTML.jpg

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