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NOP7 interacts with β-catenin and activates β-catenin/TCF signaling in hepatocellular carcinoma cells.

AbstractBACKGROUND:
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.
AuthorsNan Wu, Jing Zhao, Youhua Yuan, Chuanjia Lu, Wenjing Zhu, Qun Jiang
JournalOncoTargets and therapy (Onco Targets Ther) Vol. 11 Pg. 6369-6376 ( 2018) ISSN: 1178-6930 [Print] New Zealand
PMID30319277 (Publication Type: Journal Article)

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