| Literature DB >> 29803922 |
Wen Zhao1, Qiang Sun2, Zepeng Yu3, Shuai Mao4, Yingkang Jin1, Jiajun Li3, Zhiyi Jiang3, Yongqiang Zhang3, Mian Chen3, Peiran Chen3, Dongdong Chen3, Hailin Xu3, Shangwei Ding5, Zhiqi Yu6.
Abstract
MicroRNAs (miRNAs) play important roles in tumorigenesis and tumor progression. In this study, we investigated the role of miR-320a-3p in non-small cell lung cancer (NSCLC). Expressions of miR-320a-3p were firstly determined in 80 NSCLC patients' cancer tissues and adjacent normal lung tissues by qRT-PCR. Then MTT assay, cell migration and invasion assays were performed in vitro. Potential binding sites on target gene of miR-320a-3p were predicted and luciferase reporter assay was used to identify the potential binding sites. Tumorigenesis assay were performed in nude mice by injecting A549 cells which stably express miR-320a-3p. Results indicated that high expression of miR-320a-3p suppresses cell proliferation, migration and invasion through the inactivation of PI3K/Akt signaling pathway in NSCLC cells. Smaller tumor size and lighter weight were also found in nude mice which had miR-320a-3p higher expressed. Furthermore, data from luciferase reporter assay proved the direct binding of miR-320a-3p on the 3'UTR region of ELF3 mRNA, this could further decrease ELF3 expression transcriptionally. We provided evidence that miR-320a-3p might work as a tumor suppressor in NSCLC both in vivo and in vitro.Entities:
Keywords: ELF3; NSCLC; PI3K/Akt; miR-320a-3p
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Year: 2018 PMID: 29803922 DOI: 10.1016/j.gene.2018.05.100
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688