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MicroRNA-149 inhibits the progression of lung adenocarcinoma through targeting RAP1B and inactivating Wnt/β-catenin pathway.
- Source :
-
European review for medical and pharmacological sciences [Eur Rev Med Pharmacol Sci] 2020 May; Vol. 24 (9), pp. 4846-4854. - Publication Year :
- 2020
-
Abstract
- Objective: MicroRNAs (miRNAs) are important regulators in the progression of lung adenocarcinoma (LAD). Moreover, microRNA-149 (miR-149) exhibits different roles in human cancers. Hence, this study mainly focused on the function of miR-149 in LAD.<br />Patients and Methods: Western blot analysis and Real Time-quantitative Polymerase Chain Reaction (RT-qPCR) were used to quantify expression levels. The regulatory mechanism of miR-149/RAP1B was explored by methyl thiazolyl tetrazolium (MTT), transwell, and Dual-Luciferase reporter assays.<br />Results: Downregulation of miR-149 was detected in LAD and predicted worse prognosis in patients with LAD. Functionally, overexpression of miR-149 inhibited cell viability and metastasis in LAD. In addition, miR-149 directly targets RAP1B and restrained its expression in LAD. Furthermore, upregulation of RAP1B attenuated the inhibitory effect of miR-149 on LAD. Besides that, miR-149 blocked epithelial-mesenchymal transition (EMT) and Wnt/β-catenin pathway in LAD.<br />Conclusions: MiR-149 inhibited the progression of LAD by restraining RAP1B/EMT and inactivating Wnt/β-catenin pathway.
- Subjects :
- Adult
Aged
Cells, Cultured
Disease Progression
Female
Humans
Lung Neoplasms pathology
Male
MicroRNAs genetics
Middle Aged
rap GTP-Binding Proteins genetics
Adenocarcinoma of Lung metabolism
Adenocarcinoma of Lung pathology
Lung Neoplasms metabolism
MicroRNAs metabolism
Wnt Signaling Pathway
beta Catenin metabolism
rap GTP-Binding Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2284-0729
- Volume :
- 24
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- European review for medical and pharmacological sciences
- Publication Type :
- Academic Journal
- Accession number :
- 32432747
- Full Text :
- https://doi.org/10.26355/eurrev_202005_21173