Department of Biochemistry and Molecular Biology, Capital Medical University, Beijing, 100069, China.
Beijing Key Laboratory for Cancer Invasion and Metastasis Research, Capital Medical University, Beijing, 100069, China.
Sci Rep. 2017 Jul 17;7(1):5599. doi: 10.1038/s41598-017-06098-y.
Neddylation is a post-translational protein modification associated with cancer development. MLN4924 is a neddylation inhibitor currently under investigation in multiple phase I studies on various malignancies, and its clincal name is Pevonedistat. It has been documented that MLN4924 blocks Cullins neddylation and inactivates CRLs and, in turn, triggers cell-cycle arrest, apoptosis, senescence and autophagy in many cancer cells. In this study, we investigated the anti-tumor effect of MLN4924 in human clear cell renal carcinoma (ccRCC). Levels of both Nedd8 activating enzyme E1 and Nedd8-conjugating enzyme E2 were higher in ccRCC tissues and RCC cancer cells than in normal. Moreover, MLN4924 treatment led to rapid inhibition of Cullin1 neddylation and notably suppressed growth and survival as well as migration in a dose-and time-dependent manner. Mechanistic studies revealed that MLN4924 induced the accumulation of a number of CRL substrates, including p21, p27 and Wee1 to trigger DNA damage and induce growth arrest at the G2/M phase. MLN4924 also induced anti-migration and anti-invasion by activating E-cadherin and repressing Vimentin. Taken together, this study provides the first evidence that neddylation pathway is overactive in ccRCC and that MLN4924 induces dose-dependent anti-proliferation, anti-migration, anti-invasion in ccRCC cells. The study thus indicates that MLN4924 has potential therapeutic value for the clinical treatment of renal cancer.
Neddylation 是一种与癌症发展相关的翻译后蛋白修饰。MLN4924 是一种正在进行的多阶段 I 研究的新型靶向 NEDD8 激活酶(NAE)的小分子抑制剂,用于治疗多种恶性肿瘤,其临床名称为 Pevonedistat。已证实 MLN4924 可阻断 Cullins 的 Neddylation 并使 CRLs 失活,进而在许多癌细胞中引发细胞周期停滞、凋亡、衰老和自噬。在这项研究中,我们研究了 MLN4924 对人透明细胞肾细胞癌(ccRCC)的抗肿瘤作用。与正常组织相比,ccRCC 组织和肾透明细胞癌细胞中 Nedd8 激活酶 E1 和 Nedd8 连接酶 E2 的水平均较高。此外,MLN4924 治疗导致 Cullin1 Neddylation 的快速抑制,并以剂量和时间依赖性方式显著抑制生长和存活以及迁移。机制研究表明,MLN4924 诱导了大量 CRL 底物的积累,包括 p21、p27 和 Wee1,从而引发 DNA 损伤并在 G2/M 期诱导生长停滞。MLN4924 还通过激活 E-cadherin 和抑制 Vimentin 来诱导抗迁移和抗侵袭。总之,这项研究首次证明 Neddylation 途径在 ccRCC 中过度活跃,并且 MLN4924 诱导 ccRCC 细胞中剂量依赖性的增殖抑制、抗迁移和抗侵袭作用。因此,该研究表明 MLN4924 具有治疗肾细胞癌的潜在临床价值。