CCDC178 promotes hepatocellular carcinoma metastasis through modulation of anoikis

被引:40
作者
Hu, X. [1 ,2 ]
Zhao, Y. [1 ,2 ]
Wei, L. [3 ]
Zhu, B. [1 ,2 ]
Song, D. [1 ,2 ]
Wang, J. [1 ,2 ]
Yu, L. [1 ,2 ]
Wu, J. [1 ,2 ]
机构
[1] Fudan Univ, Zhongshan Hosp, State Key Lab Genet Engn, 2005 SongHu Rd, Shanghai 200438, Peoples R China
[2] Fudan Univ, Sch Life Sci, 2005 SongHu Rd, Shanghai 200438, Peoples R China
[3] 401 Hosp PLA, Dept Oncol, Qingdao, Peoples R China
基金
中国国家自然科学基金;
关键词
NF-KAPPA-B; CANCER; ACTIVATION; PROTEIN; GROWTH; PATHWAY; GENOME; BIM;
D O I
10.1038/onc.2017.10
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hepatocellular carcinoma (HCC) is one of the most malignant tumors with high rate of recurrence and metastasis. Coiled-coil domain-containing protein 178 (CCDC178) has been reported to be mutated in HCC, whereas its role in physiological and pathologic process, including in human cancer, remains largely unknown. Here, we found that CCDC178 is upregulated in HCC tissues and its overexpression is correlated with pathological stage (P = 0.003). CCDC178 deficiency reduced the anchorageindependent growth and anoikis resistance of HCC cells, and inhibited the HCC metastasis in vivo. Mechanistically, CCDC178 associated with BRCA1-associated protein 2 (BRAP2), a negative regulator of extracellular signal-regulated kinase (ERK) pathway, and promoted its degradation. Moreover, CCDC178 deficiency impaired the ERK activation, which is dependent on BRAP2. In conclusion, we identify CCDC178 as a novel candidate oncogene involved in anoikis resistance and HCC metastasis, and raise the possibility that CCDC178 may be a new therapeutic target for HCC.
引用
收藏
页码:4047 / 4059
页数:13
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