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E3泛素连接酶在胃癌中的功能作用

Functional roles of E3 ubiquitin ligases in gastric cancer.

作者信息

Wang Mingliang, Dai Wei, Ke Zhangyan, Li Yongxiang

机构信息

Department of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui 230032, P.R. China.

Department of Geriatric Medicine, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui 230032, P.R. China.

出版信息

Oncol Lett. 2020 Oct;20(4):22. doi: 10.3892/ol.2020.11883. Epub 2020 Jul 16.

Abstract

To date, >650 E3 ubiquitin ligases have been described in humans, including >600 really interesting new genes (RINGs), 28 homologous to E6-associated protein C-terminus (HECTs) and several RING-in-between-RINGs. They are considered key regulators and therapeutic targets of many types of human cancers, including gastric cancer (GC). Among them, some RING and HECT E3 ligases are closely related to the proliferation, infiltration and prognosis of GC. During the past few years, abnormal expressions and functions of many E3 ligases have been identified in GC. However, the functional roles of E3 ligases in GC have not been fully elucidated. The present article focuses on the functional roles of E3 ligases related to the proteasome in GC. In this comprehensive review, the latest research progress on E3 ligases involved in GC and elaborate their structure, classification, functional roles and therapeutic value in GC was summarized. Finally, 30 E3 ligases that serve essential roles in regulating the development of GC were described. Some of these ligases may serve as oncogenes or tumor suppressors in GC, whereas the pathological mechanism of others needs further study; for example, constitutive photomorphogenic 1. In conclusion, the present review demonstrated that E3 ligases are crucial tumor regulatory factors and potential therapeutic targets in GC. Therefore, more studies should focus on the therapeutic targeting of E3 ligases in GC.

摘要

迄今为止,人类已发现超过650种E3泛素连接酶,其中包括600多种真正有趣的新基因(RING)、28种与E6相关蛋白C末端同源的基因(HECT)以及几种RING中间RING基因。它们被认为是多种人类癌症(包括胃癌,GC)的关键调节因子和治疗靶点。其中,一些RING和HECT E3连接酶与胃癌的增殖、浸润及预后密切相关。在过去几年中,已在胃癌中鉴定出多种E3连接酶的异常表达和功能。然而,E3连接酶在胃癌中的功能作用尚未完全阐明。本文重点探讨与蛋白酶体相关的E3连接酶在胃癌中的功能作用。在这篇综述中,总结了E3连接酶在胃癌中的最新研究进展,并详细阐述了它们的结构、分类、在胃癌中的功能作用及治疗价值。最后,描述了30种在调节胃癌发展中起重要作用的E3连接酶。其中一些连接酶在胃癌中可能作为癌基因或肿瘤抑制因子,而其他一些的病理机制尚需进一步研究,例如组成型光形态建成蛋白1。总之,本综述表明E3连接酶是胃癌中关键的肿瘤调节因子和潜在的治疗靶点。因此,更多研究应聚焦于针对胃癌中E3连接酶的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfec/7405480/195e9150a896/ol-20-04-11883-g00.jpg

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