4.7 Review

Neddylation: a novel modulator of the tumor microenvironment

Journal

MOLECULAR CANCER
Volume 18, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/s12943-019-0979-1

Keywords

Neddylation; Tumor microenvironment; Tumor-derived factors; Cancer-associated fibroblasts; Cancer-associated endothelial cells; Immune cells

Funding

  1. Chinese Minister of Science and Technology grant [2016YFA0501800]
  2. National Thirteenth Five-Year Science and Technology Major Special Project for New Drug and Development [2017ZX09304001]
  3. National Natural Science Foundation of China [81820108022, 81625018, 81572340, 81871870, 81702244, 81802891, 81772470]
  4. Program of Shanghai Academic/Technology Research Leader [18XD1403800]
  5. Innovation Program of Shanghai Municipal Education Commission [2019-01-07-00-10-E00056]

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Neddylation, a post-translational modification that adds an ubiquitin-like protein NEDD8 to substrate proteins, modulates many important biological processes, including tumorigenesis. The process of protein neddylation is overactivated in multiple human cancers, providing a sound rationale for its targeting as an attractive anticancer therapeutic strategy, as evidence by the development of NEDD8-activating enzyme (NAE) inhibitor MLN4924 (also known as pevonedistat). Neddylation inhibition by MLN4924 exerts significantly anticancer effects mainly by triggering cell apoptosis, senescence and autophagy. Recently, intensive evidences reveal that inhibition of neddylation pathway, in addition to acting on tumor cells, also influences the functions of multiple important components of the tumor microenvironment (TME), including immune cells, cancer-associated fibroblasts (CAFs), cancer-associated endothelial cells (CAEs) and some factors, all of which are crucial for tumorigenesis. Here, we briefly summarize the latest progresses in this field to clarify the roles of neddylation in the TME, thus highlighting the overall anticancer efficacy of neddylaton inhibition.

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