| Literature DB >> 30569478 |
Jie Li1, Yingjie Li2, Bin Wang1, Yongfu Ma1, Ping Chen2.
Abstract
Long noncoding RNAs (lncRNAs) are key players in the development and progression of human cancers. The lncRNA PCAT-1 has been shown to be upregulated in human non-small cell lung cancer (NSCLC); however, its role and molecular mechanisms in NSCLC cell progression remain unclear. Here, we found that the higher expression of PCAT-1 led to a significantly poorer survival time, and multivariate analysis revealed that PCAT-1 was an independent risk factor of prognosis in NSCLC. Furthermore, we also found that the knockdown of PCAT-1 remarkably suppressed cell growth by inducing cell cycle arrest and apoptosis promotion in NSCLC cells. Moreover, the bioinformatics analysis and luciferase reporter assay revealed that PCAT-1 directly bound to the miR-149-5p, which has been reported to act as a tumor suppressor in diverse cancers. In addition, our results confirmed that the tumor-promoting effects of PCAT-1 in NSCLC cells are at least partly through negative modulation of miR-149-5p. Finally, mechanistic investigations showed that PCAT-1 upregulated the expression of miR-149-5p target gene leucine-rich repeats and immunoglobulin (Ig)-like domains 2 (LRIG2) through competitively "spongeing" miR-149-5p. Therefore, we concluded that PCAT-1 may promote the development of NSCLC through the miR-149-5p/LRIG2 axis.Entities:
Keywords: cell proliferation; leucine-rich repeats and immunoglobulin-like domains 2 (LRIG2); long noncoding RNA (lncRNA) PCAT-1; miR-149-5p; non-small cell lung cancer (NSCLC)
Year: 2018 PMID: 30569478 DOI: 10.1002/jcb.28046
Source DB: PubMed Journal: J Cell Biochem ISSN: 0730-2312 Impact factor: 4.429