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TPRG1-AS1 induces RBM24 expression and inhibits liver cancer progression by sponging miR-4691-5p and miR-3659

Authors
 Choi, Ji-Hye  ;  Kwon, So M.  ;  Moon, Sung U.  ;  Yoon, Sarah  ;  Shah, Masaud  ;  Lee, Byoung G.  ;  Yang, Jieun  ;  Park, Young Nyun  ;  Wang, Hee-Jung  ;  Woo, Hyun G. 
Citation
 Liver International, Vol.41(11) : 2788-2800, 2021-11 
Journal Title
LIVER INTERNATIONAL
ISSN
 1478-3223 
Issue Date
2021-11
Keywords
ceRNA ; HCC ; molecular subtype ; RBM24 ; RNA biotype ; TPRG1-AS1
Abstract
Background & Aims Noncoding RNAs (ncRNAs) play critical roles in hepatocellular carcinoma (HCC) progression. Here, by performing RNA-sequencing (RNA-Seq) profiling, we sought to identify novel ncRNAs that potentially drive the heterogeneous progression of liver cancers. Methods RNA-Seq profiles were obtained from 68 HCC specimens and 10 samples of adjacent non-tumour liver tissues. The functional significance of the potential driver ncRNAs was evaluated by cell experiments. Results TPRG1-AS1 was identified as a potential driver noncoding RNA that promotes heterogeneous liver cancer progression. TPRG1-AS1 induced tumour suppressor RNA-binding motif protein 24 (RBM24), suppressing tumour growth by activating apoptotic tumour cell death. In addition, we report that TPRG1-AS1 acts as a competing endogenous RNA (ceRNA) for RBM24, sponging miR-4691-5p and miR-3659 to interfere with their binding to RBM24. Conclusions We suggest that TPRG1-AS1 is a novel ceRNA sponging miR-4691-5p and miR-3659, resulting in RBM24 expression and suppression of liver cancer growth. Our results provide new insights into the functions of ncRNAs in heterogeneous HCC progression.
DOI
10.1111/liv.15026
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
Yonsei Authors
Park, Young Nyun(박영년) ORCID logo https://orcid.org/0000-0003-0357-7967
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/187320
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