Abstract |
MicroRNA-501-3p (miR-501-3p) has been reported to play tumor-suppressive roles in different cancers; however, its expression pattern and biological function in non-small cell lung cancer (NSCLC) remain unknown. In this study, we noted downregulation of miR-501-3p in NSCLC tissues and cell lines. Functional assays showed that overexpression of miR-501-3p suppressed NSCLC cell proliferation, clonogenicity, migration, and invasion. Moreover, miR-501-3p overexpression attenuated in vivo tumor growth in a nude mouse model. In terms of the mechanism, RAP1A was identified as a novel target of miR-501-3p. Overexpression of RAP1A strongly attenuated the inhibitory effects of miR-501-3p on the capacity of NSCLC cells for proliferation and motility. In the clinical samples of NSCLC, miR-501-3p levels negatively correlated with RAP1A expression, which was upregulated in NSCLC. Collectively, these results indicate that miR-501-3p acts as a tumor suppressor in NSCLC by directly targeting RAP1A mRNA and may serve as a theranostic biomarker for patients with NSCLC.
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Authors | Jinchang Lu, Lei Zhou, Bo Wu, Yanhong Duan, Yingxin Sun, Liang Gu, Donghui Xu, Chunling Du |
Journal | Experimental cell research
(Exp Cell Res)
Vol. 387
Issue 1
Pg. 111752
(02 01 2020)
ISSN: 1090-2422 [Electronic] United States |
PMID | 31805277
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2019 Elsevier Inc. All rights reserved. |
Chemical References |
- MIRN501 microRNA, human
- MicroRNAs
- RAP1A protein, human
- rap1 GTP-Binding Proteins
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Topics |
- Animals
- Carcinoma, Non-Small-Cell Lung
(genetics)
- Cell Line
- Cell Line, Tumor
- Cell Movement
(genetics)
- Cell Proliferation
(genetics)
- Down-Regulation
(genetics)
- Gene Expression Regulation, Neoplastic
(genetics)
- Genes, Tumor Suppressor
(physiology)
- HEK293 Cells
- Humans
- Lung Neoplasms
(genetics)
- Mice
- Mice, Inbred BALB C
- Mice, Nude
- MicroRNAs
(genetics)
- Up-Regulation
(genetics)
- rap1 GTP-Binding Proteins
(genetics)
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