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MLN4924 的双刃剑效应:重新思考针对泛素化途径的抗癌药物。

The Double-Edged Effects of MLN4924: Rethinking Anti-Cancer Drugs Targeting the Neddylation Pathway.

机构信息

Key Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Chongqing University, Chongqing 400044, China.

Department of Immunology, School of Basic Medical Sciences, Chengdu Medical College, Chengdu 610500, China.

出版信息

Biomolecules. 2024 Jun 21;14(7):738. doi: 10.3390/biom14070738.

DOI:10.3390/biom14070738
PMID:39062453
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11274557/
Abstract

(1) Background: The neddylation pathway assumes a pivotal role in the initiation and progression of cancer. MLN4924, a potent small-molecule inhibitor of the NEDD8-activating enzyme (NAE), effectively intervenes in the early stages of the neddylation pathway. By instigating diverse cellular responses, such as senescence and apoptosis in cancer cells, MLN4924 also exerts regulatory effects on non-malignant cells within the tumor microenvironment (TME) and tumor virus-infected cells, thereby impeding the onset of tumors. Consequently, MLN4924 has been widely acknowledged as a potent anti-cancer drug. (2) Recent findings: Nevertheless, recent findings have illuminated additional facets of the neddylation pathway, revealing its active involvement in various biological processes detrimental to the survival of cancer cells. This newfound understanding underscores the dual role of MLN4924 in tumor therapy, characterized by both anti-cancer and pro-cancer effects. This dichotomy is herein referred to as the "double-edged effects" of MLN4924. This paper delves into the intricate relationship between the neddylation pathway and cancer, offering a mechanistic exploration and analysis of the causes underlying the double-edged effects of MLN4924-specifically, the accumulation of pro-cancer neddylation substrates. (3) Perspectives: Here, the objective is to furnish theoretical support and novel insights that can guide the development of next-generation anti-cancer drugs targeting the neddylation pathway.

摘要

(1) 背景:泛素化途径在癌症的发生和发展中起着关键作用。MLN4924 是一种有效的 NEDD8-激活酶(NAE)的小分子抑制剂,能有效干预泛素化途径的早期阶段。通过引发癌细胞中的多种细胞反应,如衰老和凋亡,MLN4924 还对肿瘤微环境(TME)和肿瘤病毒感染细胞中的非恶性细胞施加调节作用,从而阻止肿瘤的发生。因此,MLN4924 被广泛认为是一种有效的抗癌药物。

(2) 最新发现:然而,最近的发现揭示了泛素化途径的更多方面,表明它积极参与了各种对癌细胞生存有害的生物学过程。这种新的认识强调了 MLN4924 在肿瘤治疗中的双重作用,既有抗癌作用,也有促癌作用。这种二分法被称为 MLN4924 的“双刃剑效应”。本文深入探讨了泛素化途径与癌症之间的复杂关系,对 MLN4924 的双刃剑效应的机制进行了探索和分析,具体来说,就是促癌泛素化底物的积累。

(3) 展望:在这里,我们的目标是提供理论支持和新的见解,以指导针对泛素化途径的下一代抗癌药物的开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf17/11274557/599d3f274f31/biomolecules-14-00738-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf17/11274557/212010091966/biomolecules-14-00738-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf17/11274557/17eb6ec283a3/biomolecules-14-00738-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf17/11274557/599d3f274f31/biomolecules-14-00738-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf17/11274557/212010091966/biomolecules-14-00738-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf17/11274557/17eb6ec283a3/biomolecules-14-00738-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf17/11274557/599d3f274f31/biomolecules-14-00738-g003.jpg

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本文引用的文献

1
Protein neddylation and its role in health and diseases.蛋白质的类泛素化及其在健康和疾病中的作用。
Signal Transduct Target Ther. 2024 Apr 5;9(1):85. doi: 10.1038/s41392-024-01800-9.
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Pharmacologic targeting of Nedd8-activating enzyme reinvigorates T-cell responses in lymphoid neoplasia.靶向 Nedd8-激活酶的药物治疗重新激活了淋巴肿瘤中的 T 细胞反应。
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Neddylation-CRLs regulate the functions of Treg immune cells.泛素化-CRLs 调节 Treg 免疫细胞的功能。
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Neddylation of HER2 Inhibits its Protein Degradation and promotes Breast Cancer Progression.HER2 的泛素化抑制其蛋白降解并促进乳腺癌进展。
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SHP2 deneddylation mediates tumor immunosuppression in colon cancer via the CD47/SIRPα axis.SHP2 去泛素化通过 CD47/SIRPα 轴介导结肠癌中的肿瘤免疫抑制。
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Hepatic neddylation deficiency triggers fatal liver injury via inducing NF-κB-inducing kinase in mice.肝内 neddylation 缺陷通过在小鼠中诱导 NF-κB 诱导激酶引发致命性肝损伤。
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NEDDylated Cullin 3 mediates the adaptive response to topoisomerase 1 inhibitors.NEDDylated Cullin 3 介导了对拓扑异构酶 1 抑制剂的适应性反应。
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A small molecule inhibitor of the UBE2F-CRL5 axis induces apoptosis and radiosensitization in lung cancer.一种 UBE2F-CRL5 轴的小分子抑制剂可诱导肺癌细胞凋亡和放射增敏。
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Neddylation pathway promotes myeloid-derived suppressor cell infiltration via NF-κB-mCXCL5 signaling in lung cancer.Neddylation途径通过NF-κB-mCXCL5信号通路促进肺癌中髓源性抑制细胞浸润。
Int Immunopharmacol. 2022 Dec;113(Pt A):109329. doi: 10.1016/j.intimp.2022.109329. Epub 2022 Oct 14.