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MiR-532-5p Suppresses Migration and Invasion of Lung Cancer Cells Through Inhibiting .
- Source :
-
Cancer Biotherapy & Radiopharmaceuticals . Nov2020, Vol. 35 Issue 9, p673-681. 9p. - Publication Year :
- 2020
-
Abstract
- Background: Studies showed that miR-532-5p suppresses proliferation and induces apoptosis of lung cancer (LC) cells; its role in LC is not fully understood. Therefore, this research aimed to reveal the effect and mechanism of miR-532-5p on migration and invasion of LC cells. Materials and Methods: The transfection efficiencies of miR-532-5p mimic, inhibitor, and overexpressed CCR4 were measured by quantitative real-time polymerase chain reaction (qRT-PCR). The relationships between miR-532-5p and CCR4 in A549 and SBC-5 cells were predicted by targetScan and verified by dual-luciferase reporter assay, Western blot, and qRT-PCR. Migration and invasion of cells transfected with miR-532-5p mimic, inhibitor, and CCR4 were determined by scratch test and transwell assay, respectively. The levels of epithelial-to-mesenchymal transition (EMT)-related proteins (E-cadherin (E-Cad)), N-catenin (N-Cad), and vimentin) in cells were measured by Western blot. Results: MiR-532-5p mimic suppressed migration and invasion, while miR-532-5p inhibitor promoted migration and invasion of cells. CCR4 was a downstream target of miR-532-5p and both its protein and mRNA expressions were inhibited by miR-532-5p mimic, but promoted by miR-532-5p inhibitor. CCR4 promoted migration, invasion, and EMT process, and such effects of CCR4 were reversed by miR-532-5p mimic. Conclusion: MiR-532-5p functioned as a cancer suppressor by negatively regulating CCR4 in LC cells, pointing to a potential protective mechanism of miR-532-5p to LC patients. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 10849785
- Volume :
- 35
- Issue :
- 9
- Database :
- Academic Search Index
- Journal :
- Cancer Biotherapy & Radiopharmaceuticals
- Publication Type :
- Academic Journal
- Accession number :
- 146945359
- Full Text :
- https://doi.org/10.1089/cbr.2019.3258