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MicroRNA‑149‑3p inhibits cell proliferation by targeting AKT2 in oral squamous cell carcinoma.
| Content Provider | Europe PMC |
|---|---|
| Author | Shen, Qin Zhu, Hong Lei, Qiaoling Chen, Luyuan Yang, Dajiang Sui, Wen |
| Copyright Year | 2020 |
| Abstract | MicroRNAs (miRs) exhibit oncogenic or tumor suppressive functions that contribute to the initiation and development of various types of human cancer. miR-149-3p has been reported to serve multiple roles in the regulation of proliferation, apoptosis and metastasis. However, the effects and detailed mechanism of miR-149-3p in oral squamous cell carcinoma (OSCC) remain unclear. In the present study, miR-149-3p mimic, mimic control, miR-149-3p inhibitor and inhibitor control were transiently transfected into Cal27 and SCC-9 cells. The viability, proliferation and apoptosis of OSCC cells were determined using Cell Counting Kit-8, colony formation and Annexin V assays, respectively. The mRNA expression levels of miR-149-3p and AKT2 were determined by reverse transcription-quantitative PCR. The protein expression levels of AKT2, cleaved caspase-3 and cleaved PARP were examined by western blot analysis. The binding of miR-149-3p to the AKT2 3′-untranslated region was evaluated by a dual luciferase reporter assay. In the present study, overexpression of miR-149-3p reduced the viability and proliferation of OSCC cells. By contrast, increased cell viability and proliferation was observed in miR-149-3p-deficient OSCC cells. Dual luciferase reporter assay indicated that miR-149-3p significantly decreased the luciferase activity of the wild-type AKT2 3′-untranslated region. Moreover, overexpression of miR-149-3p downregulated the mRNA and protein expression levels of AKT2, suggesting that miR-149-3p was a negative modulator of AKT2. Restoration of AKT2 efficiently reversed the miR-149-3p-mediated reduction in the proliferative capacity of OSCC cells. In addition, miR-149-3p enhanced the sensitivity of OSCC cells to the chemotherapeutic drug 5-fluorouracil. Taken together, the current findings revealed an inhibitory effect of miR-149-3p on the proliferation of OSCC cells through the post-transcriptional suppression of AKT2, and indicated a potential chemosensitizing function of miR-149-3p for the treatment of patients with OSCC. |
| ISSN | 17912997 |
| Journal | Molecular Medicine Reports |
| Volume Number | 23 |
| PubMed Central reference number | PMC7821286 |
| Issue Number | 3 |
| PubMed reference number | 33398370 |
| e-ISSN | 17913004 |
| DOI | 10.3892/mmr.2020.11811 |
| Language | English |
| Publisher | D.A. Spandidos |
| Publisher Date | 2021-01-05 |
| Access Restriction | Open |
| Rights License | This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. Copyright: © Shen et al. |
| Subject Keyword | oral squamous cell carcinoma microRNA-149-3p AKT2 cell proliferation |
| Content Type | Text |
| Resource Type | Article |
| Subject | Genetics Molecular Biology Biochemistry Cancer Research Molecular Medicine Oncology |