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2
Encorafenib (LGX818), a potent BRAF inhibitor, induces senescence accompanied by autophagy in BRAFV600E melanoma cells.恩考芬尼(LGX818),一种强效的 BRAF 抑制剂,可诱导 BRAFV600E 黑色素瘤细胞衰老并伴随自噬。
Cancer Lett. 2016 Jan 28;370(2):332-44. doi: 10.1016/j.canlet.2015.11.015. Epub 2015 Nov 14.
3
Phase I Study of the Investigational NEDD8-Activating Enzyme Inhibitor Pevonedistat (TAK-924/MLN4924) in Patients with Advanced Solid Tumors.TAK-924/MLN4924 治疗晚期实体瘤患者的 NEDD8 激活酶抑制剂的 I 期临床研究。
Clin Cancer Res. 2016 Feb 15;22(4):847-57. doi: 10.1158/1078-0432.CCR-15-1338. Epub 2015 Sep 30.
4
Ubiquitylation, neddylation and the DNA damage response.泛素化、类泛素化修饰与DNA损伤反应
Open Biol. 2015 Apr;5(4):150018. doi: 10.1098/rsob.150018.
5
Overactivated neddylation pathway as a therapeutic target in lung cancer.过度激活的 neddylation 通路作为肺癌的治疗靶点。
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6
MLN4924, an NAE inhibitor, suppresses AKT and mTOR signaling via upregulation of REDD1 in human myeloma cells.MLN4924是一种NAE抑制剂,它通过上调人骨髓瘤细胞中的REDD1来抑制AKT和mTOR信号传导。
Blood. 2014 May 22;123(21):3269-76. doi: 10.1182/blood-2013-08-521914. Epub 2014 Apr 8.
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Inactivation of SAG/RBX2 E3 ubiquitin ligase suppresses KrasG12D-driven lung tumorigenesis.SAG/RBX2 E3 泛素连接酶的失活抑制 KrasG12D 驱动的肺肿瘤发生。
J Clin Invest. 2014 Feb;124(2):835-46. doi: 10.1172/JCI70297. Epub 2014 Jan 16.
9
Overcoming platinum resistance in preclinical models of ovarian cancer using the neddylation inhibitor MLN4924.使用泛素化抑制剂 MLN4924 克服卵巢癌临床前模型中的铂耐药性。
Mol Cancer Ther. 2013 Oct;12(10):1958-67. doi: 10.1158/1535-7163.MCT-12-1028. Epub 2013 Aug 12.
10
Disrupting protein NEDDylation with MLN4924 is a novel strategy to target cisplatin resistance in ovarian cancer.用 MLN4924 破坏蛋白质的 NEDDylation 是一种针对卵巢癌顺铂耐药的新策略。
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MLN4924(一种NEDDylation抑制剂)可促进耐紫杉醇的人肺腺癌细胞死亡。

MLN4924 neddylation inhibitor promotes cell death in paclitaxel-resistant human lung adenocarcinoma cells.

作者信息

Xu Qiang, Lin Guibin, Xu Huizhe, Hu Lulu, Wang Yupeng, Du Sha, Deng Wuguo, Hu Wenxian, Cheng Wei, Jiang Ke

机构信息

Department of Orthopedics, The Affiliated Yuhuangding Hospital of Qingdao University Medical College, Yantai, Shandong 264000, P.R. China.

Institute of Cancer Stem Cell, Dalian Medical University Cancer Center, Dalian, Liaoning 116044, P.R. China.

出版信息

Oncol Lett. 2018 Jan;15(1):515-521. doi: 10.3892/ol.2017.7314. Epub 2017 Nov 1.

DOI:10.3892/ol.2017.7314
PMID:29387232
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5768125/
Abstract

Acquired resistance to first-line chemotherapeutics, including paclitaxel (PTX), is a primary factor contributing to chemotherapy failure in non-small cell lung cancer (NSCLC) patients. Previous studies have identified that targeting NEDD8-activating enzyme (NAE) with MLN4924 effectively overcomes platinum resistance in preclinical models of ovarian cancer. However, the underlying mechanisms are yet to be fully elucidated. The present study demonstrates that the inhibition of the neddylation pathway with MLN4924 an NAE inhibitor inhibited protein neddylation, inactivated cullin-RING E3 ligase and exhibited a potent antiproliferative effect on PTX-resistant A549 and H460 cells (A549/PTX and H460/PTX). The application of MLN4924 promotes apoptosis and DNA damage in A549/PTX and H460/PTX cells. Additionally, MLN4924 abrogated the 3-dimensional growth potential of these cells and inhibited the formation of the A549/PTX and H460/PTX spheroids. Notably, combining MLN4924 with PTX did not exhibit synergy in PTX-resistant NSCLC cells. Taken together, the results of the current study suggest that MLN4924 may be utilized as an effective strategy for the treatment of PTX-resistant NSCLC.

摘要

对包括紫杉醇(PTX)在内的一线化疗药物产生获得性耐药是导致非小细胞肺癌(NSCLC)患者化疗失败的主要因素。先前的研究已证实,在卵巢癌临床前模型中,使用MLN4924靶向NEDD8激活酶(NAE)可有效克服铂耐药。然而,其潜在机制尚未完全阐明。本研究表明,使用NAE抑制剂MLN4924抑制NEDDylation途径可抑制蛋白质NEDDylation,使cullin-RING E3连接酶失活,并对PTX耐药的A549和H460细胞(A549/PTX和H460/PTX)表现出强大的抗增殖作用。MLN4924的应用促进了A549/PTX和H460/PTX细胞的凋亡和DNA损伤。此外,MLN4924消除了这些细胞的三维生长潜力,并抑制了A549/PTX和H460/PTX球体的形成。值得注意的是,在PTX耐药的NSCLC细胞中,将MLN4924与PTX联合使用未表现出协同作用。综上所述,本研究结果表明,MLN4924可能是治疗PTX耐药NSCLC的有效策略。