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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.

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。

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