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用MLN4924(培澳新)靶向NEDDylation途径可诱导肾细胞癌中依赖NOXA的细胞凋亡。

Targeting neddylation pathway with MLN4924 (Pevonedistat) induces NOXA-dependent apoptosis in renal cell carcinoma.

作者信息

Wang Jiyou, Wang Shiwen, Zhang Wenjuan, Wang Xiaofang, Liu Xiaojun, Liu Liang, Li Lihui, Liang Yupei, Yu Jinha, Jeong Lak Shin, Jia Lijun, Zhao Hu, Zhang Yanmei

机构信息

Department of Laboratory Medicine, Huadong Hospital Affiliated to Fudan University, Shanghai, 200040, China; College of Life Science, Dezhou University, Dezhou, 253023, China.

Department of Laboratory Medicine, Huadong Hospital Affiliated to Fudan University, Shanghai, 200040, China; Shanghai Key Laboratory of Clinical Geriatric Medicine, Shanghai, 200040, China; Research Center on Aging and Medicine, Fudan University, Shanghai, 200040, China.

出版信息

Biochem Biophys Res Commun. 2017 Sep 2;490(4):1183-1188. doi: 10.1016/j.bbrc.2017.06.179. Epub 2017 Jun 29.

Abstract

Inhibition of protein neddylation pathway has emerged an attractive anticancer strategy in preclinical studies by using Nedd8-activating enzyme (NAE) inhibitor MLN4924 (Pevonedistat). Previous studies have reported the antitumor activity of MLN4924 mediated by its efficacy on apoptosis, autophagy and senescence. However, whether MLN4924 has any effect on renal carcinoma cells (RCC) remains unexplored. Here we reported that MLN4924 specifically inhibited protein neddylation pathway, leading to statistically significantly suppress the proliferation, survival and migration of RCC cells by inducing G cell-cycle arrest, followed by apoptosis in a MLN4924 dose-dependent manner. Further mechanistic study revealed that MLN4924-induced apoptosis was mediated by substantial up-regulation of pro-apoptotic NOXA. These findings highlighted the anticancer effects of the neddylation inhibitors (e.g. MLN4924) for the treatment of RCC.

摘要

在临床前研究中,通过使用Nedd8激活酶(NAE)抑制剂MLN4924(培沃替尼)抑制蛋白质Nedd化途径已成为一种有吸引力的抗癌策略。先前的研究报道了MLN4924通过其对细胞凋亡、自噬和衰老的作用介导的抗肿瘤活性。然而,MLN4924对肾癌细胞(RCC)是否有任何影响仍未得到探索。在此,我们报道MLN4924特异性抑制蛋白质Nedd化途径,导致通过诱导G期细胞周期停滞,以MLN4924剂量依赖性方式显著抑制RCC细胞的增殖、存活和迁移,随后诱导细胞凋亡。进一步的机制研究表明,MLN4924诱导的细胞凋亡是由促凋亡蛋白NOXA的大量上调介导的。这些发现突出了Nedd化抑制剂(如MLN4924)对RCC治疗的抗癌作用。

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