| Literature DB >> 29899407 |
Gun-Woo Lee1, Jun Bum Park1, Sung Yeon Park1,2, Jieun Seo1, Seung-Hyun Shin1, Jong-Wan Park1,2, Sang Jung Kim1,2,3, Masatoshi Watanabe4, Yang-Sook Chun5,6,7.
Abstract
Neddylation is a cellular process that covalently conjugates substrate proteins with the small ubiquitin-like molecule NEDD8. As neddylation is required for fast turnover of proteins in proliferating cancer cells, the neddylation process is currently regarded as a potential target for cancer therapy. However, little is known about the role of neddylation in cancer invasion and metastasis. Unexpectedly, we here found that the neddylation blockade stimulates migration of lung cancer and glioblastoma cells. Mechanistically, C-CBL acts as the E3 ligase for neddylation of the proto-oncogene c-Src. After neddylation, c-Src is poly-ubiquitinated and degraded through the proteasome, which inhibits the PI3K-AKT pathway responsible for cell migration. In human lung cancer tissues, the downregulation of C-CBL was associated with c-Src/AKT, cancer metastasis, and poor survival in patients. Therefore, C-CBL is likely to play a tumor suppressive role by antagonizing a robust oncogenic signaling driven by c-Src. This study provides new insight about the role of neddylation in cancer metastasis. It also implies that the metastasis risk should be carefully evaluated before the clinical application of neddylation inhibitors as anticancer regimens.Entities:
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Year: 2018 PMID: 29899407 DOI: 10.1038/s41388-018-0354-5
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867