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Role of UPF1 in lncRNA-HEIH regulation for hepatocellular carcinoma therapyopen access

Authors
Cha, HyunhoKim, MinwooAhn, NaraeJeong, Seong DongIgnatova, ElizavetaChi, Sung WookKim, Hyeon HoHwang, Jungwook
Issue Date
Feb-2024
Publisher
Springer Nature
Citation
Experimental & Molecular Medicine, v.56, no.2, pp 344 - 354
Pages
11
Indexed
SCIE
SCOPUS
KCI
Journal Title
Experimental & Molecular Medicine
Volume
56
Number
2
Start Page
344
End Page
354
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/197472
DOI
10.1038/s12276-024-01158-6
ISSN
1226-3613
2092-6413
Abstract
UPF1, a novel posttranscriptional regulator, regulates the abundance of transcripts, including long noncoding RNAs (lncRNAs), and thus plays an important role in cell homeostasis. In this study, we revealed that UPF1 regulates the abundance of hepatocellular carcinoma upregulated EZH2-associated lncRNA (lncRNA-HEIH) by binding the CG-rich motif, thereby regulating hepatocellular carcinoma (HCC) tumorigenesis. UPF1-bound lncRNA-HEIH was susceptible to degradation mediated by UPF1 phosphorylation via SMG1 and SMG5. According to analysis of RNA-seq and public data on patients with liver cancer, the expression of lncRNA-HEIH increased the levels of miR-194-5p targets and was inversely correlated with miR-194-5p expression in HCC patients. Furthermore, UPF1 depletion upregulated lncRNA-HEIH, which acts as a decoy of miR-194-5p that targets GNA13, thereby promoting GNA13 expression and HCC proliferation. The UPF1/lncRNA-HEIH/miR-194-5p/GNA13 regulatory axis is suggested to play a crucial role in cell progression and may be a suitable target for HCC therapy.
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GRADUATE SCHOOL OF BIOMEDICAL SCIENCE AND ENGINEERING (DEPARTMENT OF BIOMEDICAL SCIENCE)
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