AI Article Synopsis

  • - Neddylation is a process that adds a small molecule (NEDD8) to proteins, which is important for destroying proteins in rapidly growing cancer cells and is being explored as a cancer treatment target.
  • - Blocking neddylation surprisingly stimulates the migration of lung cancer and glioblastoma cells by preventing the degradation of the proto-oncogene c-Src, leading to increased activation of the PI3K-AKT pathway involved in cell movement.
  • - The study highlights the role of C-CBL, which helps neddylate c-Src, as a potential tumor suppressor, suggesting that caution is needed when using neddylation inhibitors in cancer therapy due to possible increased metastasis risk.

Article 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.

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http://dx.doi.org/10.1038/s41388-018-0354-5DOI Listing

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