Accumulating evidence has suggested that microRNAs (miRNAs) play important roles in regulating the progression of cancerby acting as tumor suppressors or oncogenes. Here, our results demonstrated that miR-5582-5p was significantly down-regulated in non-small cell lung cancer (NSCLC) tissues and cell lines compared with normal controls. Overexpression of miR-5582-5p markedly inhibited the proliferation and migration of NSCLC cells. Consistently, the apoptosis of NSCLC cells was also significantly promoted by overexpressed miR-5582-5p. Functional study uncovered that miR-5582-5p bound the 3'-untranslated region (UTR) of fibroblastic growth factor-10 (FGF-10) and decreased the expression of FGF-10 in NSCLC cells. FGF-10 was up-regulated in NSCLC tissues and inversely correlated with the level of miR-5582-5p in NSCLC tissues. Overexpression of FGF-10 significantly reversed the inhibitory effect of miR-5582-5p on the proliferation of NSCLC cells. Taken together, our results demonstrated the functional mechanism of miR-5582-5p in suppressing malignant behaviors of NSCLC cells by targeting FGF-10. These findings demonstrated that miR-5582-5p might be a novel therapeutic target in the treatment of NSCLC.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6945143 | PMC |
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