Abstract | BACKGROUND: The hyperactivation of β- catenin signaling is frequently observed in clinical hepatocellular carcinoma (HCC) samples. Further understanding the mechanisms involved in activating β- catenin/TCF signaling would benefit the treatment of HCC. METHOD AND RESULTS: Here, it was found that NOP7 was a binding partner of β- catenin. NOP7 strengthened the interaction between β- catenin and TCF4, which led to the activation of β- catenin/TCF signaling. The upregulation of NOP7 in HCC promoted the growth (in both liquid culture and soft agar) and migration of HCC cancer cells. CONCLUSION: Taken together, we have demonstrated the oncogenic functions of NOP7 in HCC, suggesting that targeting NOP7 would benefit the treatment of HCC.
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Authors | Nan Wu, Jing Zhao, Youhua Yuan, Chuanjia Lu, Wenjing Zhu, Qun Jiang |
Journal | OncoTargets and therapy
(Onco Targets Ther)
Vol. 11
Pg. 6369-6376
( 2018)
ISSN: 1178-6930 [Print] New Zealand |
PMID | 30319277
(Publication Type: Journal Article)
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