| Literature DB >> 31148184 |
Geng Qin1, Xinyi Tu1,2,3, Haibei Li3, Pengbo Cao1, Xi Chen1, Jin Song1, Hui Han1, Yuanfeng Li1, Bingqian Guo1, Liting Yang1, Pandeng Yan1, Peiyao Li1, Chengming Gao1, Jinxu Zhang1, Ying Yang1, Jian Zheng4, Huai-Qiang Ju4, Lei Lu5, Xuan Wang5, Chaohui Yu6, Yi Sun7, Baocai Xing7, Hongzan Ji8, Dongxin Lin4, Fuchu He2,3, Gangqiao Zhou1,9.
Abstract
To identify hepatocellular carcinoma (HCC)-implicated long noncoding RNAs (lncRNAs), we performed an integrative omics analysis by integrating mRNA and lncRNA expression profiles in HCC tissues. We identified a collection of candidate HCC-implicated lncRNAs. Among them, we demonstrated that an lncRNA, which is named as p53-stabilizing and activating RNA (PSTAR), inhibits HCC cell proliferation and tumorigenicity through inducing p53-mediated cell cycle arrest. We further revealed that PSTAR can bind to heterogeneous nuclear ribonucleoprotein K (hnRNP K) and enhance its SUMOylation and thereby strengthen the interaction between hnRNP K and p53, which ultimately leads to the accumulation and transactivation of p53. PSTAR is down-regulated in HCC tissues, and the low PSTAR expression predicts poor prognosis in patients with HCC, especially those with wild-type p53.Entities:
Year: 2019 PMID: 31148184 DOI: 10.1002/hep.30793
Source DB: PubMed Journal: Hepatology ISSN: 0270-9139 Impact factor: 17.425