| Literature DB >> 31298469 |
Sheng Xue1, Sheng Wang1, Jian Li1, Han Guan1, Shengqun Jiang2, Yuanyuan Guo1, Qingwen Li1.
Abstract
Long non-coding RNA (LncRNA) neuroblastoma associated transcript 1 (NBAT1) was demonstrated to be significantly downregulated in renal carcinoma (RCC) cells. However, the function and mechanism of NBAT1 in RCC is poorly understood. The expression of NBAT1 and glycogen synthase kinase-3β (GSK-3β)-mediated Wnt/β-catenin-related proteins were measured by quantitative real-time PCR (qRT-PCR) and western blotting in RCC cell lines. Cell viability, migration, and invasion were estimated by CCK-8 and Transwell assay. The association of miR-346 with GSK-3β expression was verified using luciferase assay. NBAT1 was significantly downregulated in RCC cells, and inhibited RCC cell proliferation, migration, and invasion. Furthermore, NBAT1 negatively regulated miR-346 expression. In addition, miR-346 overexpression and the knockdown of GSK-3β, a direct target of miR-346 could overturn the inhibitory effect of NBAT1 on Wnt/β-catenin signaling and cell proliferation, migration, and invasion. NBAT1 functioned as an endogenous sponge by competing for miR-346 binding to GSK-3β and therefore alleviated RCC cells.Entities:
Keywords: GSK-3β; NBAT1; long non-coding RNA; miR-346; renal carcinoma
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Year: 2019 PMID: 31298469 DOI: 10.1002/iub.2111
Source DB: PubMed Journal: IUBMB Life ISSN: 1521-6543 Impact factor: 3.885