1. Academic Validation
  2. Neddylation inhibitor MLN4924 induces G2 cell cycle arrest, DNA damage and sensitizes esophageal squamous cell carcinoma cells to cisplatin

Neddylation inhibitor MLN4924 induces G2 cell cycle arrest, DNA damage and sensitizes esophageal squamous cell carcinoma cells to cisplatin

  • Oncol Lett. 2018 Feb;15(2):2583-2589. doi: 10.3892/ol.2017.7616.
Shan Lin 1 Zhaoyang Shang 1 Shuo Li 1 Peng Gao 1 Yi Zhang 1 Shuaiheng Hou 1 Peng Qin 2 Ziming Dong 1 Tao Hu 1 Ping Chen 1
Affiliations

Affiliations

  • 1 Department of Basic Science of Oncology, College of Basic Medical Sciences, Zhengzhou University, Collaborative Innovation Center of Henan Province for Cancer Chemoprevention, Zhengzhou, Henan 450001, P.R. China.
  • 2 Department of Immunotherapy, Henan Cancer Hospital and Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, Henan 450008, P.R. China.
Abstract

Inhibiting the protein neddylation pathway using the NEDD8-activating Enzyme Inhibitor MLN4924 represents an attractive Anticancer strategy having been demonstrated to exhibit promising Anticancer efficacy and with tolerable levels of toxicity; however, the mechanism by which MLN4924 inhibits cell proliferation in human esophageal squamous cell carcinoma (ESCC) cells requires further investigation. The present study revealed that MLN4924 treatment led to G2 cell cycle arrest and enhanced the protein stability of Wee1-like protein kinase and cyclin dependent protein kinase inhibitor 1A and B and p27. Furthermore, MLN4924 induced DNA damage and sensitized esophageal Cancer cells to cisplatin by enhancing Apoptosis. These findings extend the understanding of the function and mechanism of MLN4924 in ESCC and provide further evidence for the future development of neddylation inhibitors in clinical trials of esophageal Cancer therapy, either alone or in combination.

Keywords

Cullin-RING ligase; MLN4924; esophageal squamous cell carcinoma; neddylation.

Figures
Products