| Literature DB >> 31079325 |
Yanwei Cui1,2, Lei Zhao1,2, Shilei Zhao1,2, Tao Guo1,2, Fengzhou Li1,2, Zhuoshi Li1,2, Lei Fang1,2, Taihua Wu3, Chundong Gu4,5.
Abstract
Previous studies have reported that microRNA-30e (miR-30e) is dysregulated in multiple human cancers. However, the expression, functions and molecular mechanism of miR-30e in NSCLC remain unknown. In this study, we found that miR-30e was expressed at a low level in NSCLC tissues and cell lines. In NSCLC cell lines, enforced expression of miR-30e could inhibit cell proliferation and invasion in vitro. In addition, miR-30e negatively regulated SOX9 expression through directly binding to the 3'UTR of SOX9, and an inverse correlation was found between miR-30e and SOX9 mRNA expression in NSCLC tissues. Moreover, knockdown of SOX9 led to decreased proliferation and invasion of NSCLC cells. Taken together, miR-30e acts as a tumor suppressor in NSCLC, and inhibits cell proliferation and invasion possibly by directly targeting SOX9. These findings might provide novel therapeutic targets for NSCLC.Entities:
Keywords: Invasion; MicroRNA-30e; Non-small cell lung cancer; Proliferation; SOX9
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Year: 2019 PMID: 31079325 DOI: 10.1007/s13577-018-0223-0
Source DB: PubMed Journal: Hum Cell ISSN: 0914-7470 Impact factor: 4.174