| Literature DB >> 31599491 |
Jianming Tang1, Bo Yu1, Yanxin Li2, Weiwei Zhang1, Angel A Alvarez3, Bo Hu3, Shi-Yuan Cheng3, Haizhong Feng1.
Abstract
Long non-coding RNAs (lncRNAs) are critical regulators in cancer. However, the involvement of lncRNAs in TGF-β-regulated tumorigenicity is still unclear. Here, we identify TGF-β-activated lncRNA LINC00115 as a critical regulator of glioma stem-like cell (GSC) self-renewal and tumorigenicity. LINC00115 is upregulated by TGF-β, acts as a miRNA sponge, and upregulates ZEB1 by competitively binding of miR-200s, thereby enhancing ZEB1 signaling and GSC self-renewal. LINC00115 also promotes ZNF596 transcription by preventing binding of miR-200s to the 5'-UTR of ZNF596, resulting in augmented ZNF596/EZH2/STAT3 signaling and GBM tumor growth. Inhibition of EZH2 by genetic approaches or a small molecular inhibitor markedly suppresses LINC00115-driven GSC self-renewal and tumorigenicity. Moreover, LINC00115 is highly expressed in GBM, and LINC00115 expression or correlated co-expression with ZEB1 or ZNF596 is prognostic for clinical GBM survival. Our work defines a critical role of LINC00115 in GSC self-renewal and tumorigenicity, and suggests LINC00115 as a potential target for GBM treatment.Entities:
Keywords: EZH2; ZEB1; ZNF596; glioma stem-like cell; lncRNA LINC00115
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Year: 2019 PMID: 31599491 PMCID: PMC6893290 DOI: 10.15252/embr.201948170
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807