miR-338-5p inhibits cell growth and migration via inhibition of the METTL3/m6A/c-Myc pathway in lung cancer
Autor: | Ren Zhu, Fangjuan Li, Hongyu Wu |
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Rok vydání: | 2020 |
Předmět: |
Lung Neoplasms
Biophysics Treatment of lung cancer Biochemistry Proto-Oncogene Proteins c-myc 03 medical and health sciences 0302 clinical medicine Downregulation and upregulation Western blot medicine Gene silencing Humans RNA Neoplasm Lung cancer 030304 developmental biology 0303 health sciences medicine.diagnostic_test business.industry Cell growth Cancer General Medicine Methyltransferases respiratory system medicine.disease Gene Expression Regulation Neoplastic MicroRNAs Real-time polymerase chain reaction A549 Cells 030220 oncology & carcinogenesis Cancer research business Signal Transduction |
Zdroj: | Acta biochimica et biophysica Sinica. 53(3) |
ISSN: | 1745-7270 |
Popis: | Lung cancer is a common type of cancer that causes a very large public health burden worldwide. Achieving a better understanding of the molecular mechanism underlying the progression of lung cancer is of benefit for the diagnosis, prognosis, and treatment of lung cancer. Here, we first identified dramatically decreased expression of miR-338-5p in lung cancer tissues and cells using quantitative polymerase chain reaction (qPCR) analysis. We then revealed that miR-338-5p inhibited the cell growth and migration of lung cancer cells using cell counting kit 8 (CCK8), EdU, and Transwell analysis. Furthermore, we demonstrated that miR-338-5p inhibited METTL3 expression by qPCR, western blot analysis, and luciferase reporter assay, while upregulation of METTL3 alleviated the role of miR-338-5p in lung cancer cells. We also showed that METTL3 promoted c-Myc expression by increasing the m6A modification of c-Myc, and overexpression of c-Myc restored the inhibition of cell growth and migration of lung cancer cells induced by METTL3 silencing. Ultimately, this research illustrated that modification of the miR-338-5p/METTL3/c-Myc pathway affected cellular progression in lung cancer cells. Collectively, our study revealed the underlying mechanism of miR-338-5p in lung cancer, providing a novel regulatory pathway in lung cancer. There is potential for this pathway to serve as a diagnostic, prognostic, and therapeutic biomarker for lung cancer. |
Databáze: | OpenAIRE |
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