| Literature DB >> 28669728 |
Jiyou Wang1, Shiwen Wang2, Wenjuan Zhang3, Xiaofang Wang3, Xiaojun Liu3, Liang Liu3, Lihui Li3, Yupei Liang3, Jinha Yu4, Lak Shin Jeong4, Lijun Jia5, Hu Zhao6, Yanmei Zhang7.
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 G2 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.Entities:
Keywords: Apoptosis; MLN4924; Neddylation; Renal cell carcinoma
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Year: 2017 PMID: 28669728 DOI: 10.1016/j.bbrc.2017.06.179
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575