Department of Biomedical Science, Seoul, 110-799, Korea.
Ischemic/Hypoxic Disease Institute, Seoul, 110-799, Korea.
Oncogene. 2018 Oct;37(41):5552-5568. doi: 10.1038/s41388-018-0354-5. Epub 2018 Jun 13.
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.
类泛素化是一种将底物蛋白与小泛素样蛋白 NEDD8 共价连接的细胞过程。由于类泛素化对于增殖癌细胞中蛋白质的快速周转是必需的,因此类泛素化过程目前被认为是癌症治疗的潜在靶点。然而,关于类泛素化在癌症侵袭和转移中的作用知之甚少。出乎意料的是,我们在这里发现类泛素化阻断会刺激肺癌和神经胶质瘤细胞的迁移。在机制上,C-CBL 作为原癌基因 c-Src 类泛素化的 E3 连接酶。类泛素化后,c-Src 通过蛋白酶体被多泛素化和降解,从而抑制负责细胞迁移的 PI3K-AKT 途径。在人类肺癌组织中,C-CBL 的下调与 c-Src/AKT、癌症转移和患者的不良生存相关。因此,C-CBL 可能通过拮抗由 c-Src 驱动的强大致癌信号发挥肿瘤抑制作用。这项研究为类泛素化在癌症转移中的作用提供了新的见解。它还暗示在将类泛素化抑制剂作为抗癌方案用于临床之前,应仔细评估转移风险。