Unveiling the role of UPF3B in hepatocellular carcinoma: Potential therapeutic target

Author:

Hou Bowen1,Shu Min1ORCID,Liu Chenghao1ORCID,Du Yunfeng1,Xu Cuicui1,Jiang Huijiao12,Hou Jun12,Chen Xueling12,Wang Lianghai12ORCID,Wu Xiangwei12

Affiliation:

1. NHC Key Laboratory of Prevention and Treatment of Central Asia High Incidence Diseases The First Affiliated Hospital/Shihezi University School of Medicine Shihezi China

2. Key Laboratory of Xinjiang Endemic and Ethnic Diseases Shihezi University School of Medicine Shihezi China

Abstract

AbstractRNA‐binding proteins can regulate nucleotide metabolism and gene expression. UPF3B regulator of nonsense mediated mRNA decay (UPF3B) exhibits dysfunction in cancers. However, its role in the progression of hepatocellular carcinoma (HCC) is still insufficiently understood. Here, we found that UPF3B was markedly upregulated in HCC samples and associated with adverse prognosis in patients. UPF3B dramatically promoted HCC growth both in vivo and in vitro. Mechanistically, UPF3B was found to bind to PPP2R2C, a regulatory subunit of PP2A, boosting its mRNA degradation and activating the PI3K/AKT/mTOR pathway. E2F transcription factor 6 (E2F6) directly binds to the UPF3B promoter to facilitate its transcription. Together, the E2F6/UPF3B/PPP2R2C axis promotes HCC growth through the PI3K/AKT/mTOR pathway. Hence, it could be a promising therapeutic target for treating HCC.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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