Sun Jian, Liu Cui, Lang Changhui, Wang Jing, Li Qingxiang, Peng Chang, Du Zuochen, Chen Yan, Huang Pei
Department of Pediatrics, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, 563000, China.
Department of Pediatrics, Guizhou Children's Hospital, Zunyi, Guizhou, 563000, China.
J Pharm Anal. 2025 May;15(5):101140. doi: 10.1016/j.jpha.2024.101140. Epub 2024 Nov 8.
Neddylation is a crucial posttranslational modification that involves the attachment of neural precursor cell-expressed developmentally downregulated protein 8 (NEDD8) to a lysine residue in the substrate via the sequential actions of the E1 NEDD8-activating enzyme (NAE) (E1), E2 NEDD8-conjugating enzyme (E2), and E3 NEDD8-ligase (E3). The most extensively studied substrates of neddylation are members of the cullin family, which act as scaffold components for cullin ring E3 ubiquitin ligases (CRLs). Since cullin neddylation activates CRLs, which are frequently overactive in tumors, inhibiting neddylation has emerged as a promising strategy for developing novel antitumor therapies. This review explores the antitumor effects of inhibiting neddylation that leads to the inactivation of CRLs and provides a summary of known inhibitors that target protein-protein interactions (PPIs) within the neddylation enzymatic cascade.
Neddylation是一种关键的翻译后修饰,它涉及通过E1 NEDD8激活酶(NAE)(E1)、E2 NEDD8缀合酶(E2)和E3 NEDD8连接酶(E3)的顺序作用,将神经前体细胞表达的发育下调蛋白8(NEDD8)连接到底物中的赖氨酸残基上。Neddylation研究最广泛的底物是cullin家族成员,它们作为cullin环E3泛素连接酶(CRL)的支架成分。由于cullin neddylation激活CRL,而CRL在肿瘤中经常过度活跃,抑制neddylation已成为开发新型抗肿瘤疗法的一种有前景的策略。本文综述探讨了抑制neddylation导致CRL失活的抗肿瘤作用,并总结了针对neddylation酶促级联反应中蛋白质-蛋白质相互作用(PPI)的已知抑制剂。