作者: Cuicui Li , Long Wu , Pengpeng Liu , Kun Li , Zhonglin Zhang
DOI: 10.7150/THNO.47677
关键词: Cyclin-dependent kinase 1 、 RNA 、 Downregulation and upregulation 、 Cancer research 、 KEGG 、 Carcinogenesis 、 Small nucleolar RNA 、 Cell Cycle Gene 、 Biology 、 Cell culture
摘要: Rationale: Understanding the roles of small nucleolar RNAs (snoRNAs) in hepatocarcinogenesis will provide new avenues to identify diagnostic and therapeutic targets for hepatocellular carcinoma (HCC). Our previous research confirmed tumor-suppressive effect Up-frameshift 1 (Upf1) HCC. Herein, we examined expression profiles snoRNAs regulated by Upf1 hepatoma cells. Methods: We cells using RNA-sequencing analysis then investigated significance SNORD52 HCC tissue different cell lines. The protumorigenic effects on were both vitro vivo gain-of-function loss-of-function assays. RNA pull-down assays mass spectrometry used RNA-binding protein that binds SNORD52. Results: Many identified; one which, human C/D box SNORD52, was upregulated tissues negatively correlated with expression, patients higher had a poor clinical prognosis. promoted tumorigenesis vivo. Mechanistically, KEGG showed series cycle genes further CDK1 enhancing stability proteins function depends presence CDK1. Conclusion: Overall, present study indicates could be potential biomarker Targeting Upf1/SNORD52/CDK1 pathway might have