4.6 Article

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

期刊

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2017.06.179

关键词

Neddylation; MLN4924; Renal cell carcinoma; Apoptosis

资金

  1. Chinese Minister of Science and Technology [2016YFA0501800]
  2. National Natural Science Foundation China [81602072, 81625081, 81372196, 81572340, 81400893]
  3. Shanghai Education Development Foundation [14SG07]
  4. Shanghai Sailing Program [2017YF1405000]
  5. Shanghai Municipal Commission of Health and Family Planning, Key developing disciplines [2015Z130501]

向作者/读者索取更多资源

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(2) 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 proapoptotic NOXA. These findings highlighted the anticancer effects of the neddylation inhibitors (e.g. MLN4924) for the treatment of RCC. (C) 2017 Published by Elsevier Inc.

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