Yu Zongdong, Li Hong, Zhu Jie, Wang Haibiao, Jin Xiaofeng
Department of Biochemistry and Molecular Biology, Zhejiang Key Laboratory of Pathophysiology, Medical School of Ningbo University Ningbo 315211, Zhejiang, China.
Department of Hepatobiliary and Pancreatic Surgery, Ningbo Medical Center of Lihuili Hospital, Ningbo University Ningbo 315040, Zhejiang, China.
Am J Cancer Res. 2022 Mar 15;12(3):1179-1214. eCollection 2022.
Hepatocarcinogenesis is a complex multistep biological process involving genetic and epigenetic alterations that are accompanied by activation of oncoproteins and inactivation of tumor suppressors, which in turn results in Hepatocellular carcinoma (HCC), one of the common tumors with high morbidity and mortality worldwide. The ubiquitin-proteasome system (UPS) is the key to protein degradation and regulation of physiological and pathological processes, and E3 ligases are key enzymes in the UPS that contain a variety of subfamily proteins involved in the regulation of some common signal pathways in HCC. There is growing evidence that many structural or functional dysfunctions of E3 are engaged in the development and progression of HCC. Herein, we review recent research advances in HCC-associated E3 ligases, describe their structure, classification, functional roles, and discuss some mechanisms of the abnormal activation or inactivation of the HCC-associated signal pathway due to the binding of E3 to known substrates. In addition, given the success of proteasome inhibitors in the treatment of malignant cancers, we characterize the current knowledge and future prospects for targeted therapies against aberrant E3 in HCC.
肝癌发生是一个复杂的多步骤生物学过程,涉及基因和表观遗传改变,同时伴有癌蛋白激活和肿瘤抑制因子失活,进而导致肝细胞癌(HCC),这是全球发病率和死亡率都很高的常见肿瘤之一。泛素-蛋白酶体系统(UPS)是蛋白质降解以及生理和病理过程调节的关键,而E3连接酶是UPS中的关键酶,包含多种亚家族蛋白,参与肝癌中一些常见信号通路的调节。越来越多的证据表明,E3的许多结构或功能功能障碍都与肝癌的发生和发展有关。在此,我们综述了肝癌相关E3连接酶的最新研究进展,描述了它们的结构、分类、功能作用,并讨论了由于E3与已知底物结合导致肝癌相关信号通路异常激活或失活的一些机制。此外,鉴于蛋白酶体抑制剂在恶性肿瘤治疗中的成功,我们阐述了针对肝癌中异常E3的靶向治疗的现有知识和未来前景。