[No authors listed]
Accumulating evidence indicates that microRNAs (miRs) are important regulators in a number of types of human cancer, including nonâsmall cell lung cancer (NSCLC). The function of miRâ3120â5p in NSCLC remains unclear. In the present study, it was demonstrated that miRâ3120â5p was significantly upregulated in NSCLC tissues. Additionally, miRâ3120â5p expression level was positively associated with NSCLC metastasis and tumor, node and metastasis stage. Furthermore, it was demonstrated that miRâ3120â5p exhibited potential as an indicator of NSCLC for use in diagnosis. Through functional experiments, it was demonstrated that overexpression of miRâ3120â5p promoted the proliferation, colony formation and invasion of NSCLC cells. miRâ3120â5p overexpression significantly promoted cell cycle progression. Mechanistically, it was demonstrated that Krueppelâlike factor 4 (KLF4) was a target of miRâ3120â5p in NSCLC cells. Overexpression of miRâ3120â5p repressed the expression of KLF4 in A549 and H460 cells. Furthermore, it was demonstrated that KLF4 was downregulated in NSCLC tissues and cell lines. Overexpression of KLF4 significantly reversed the effects of miRâ3120â5p on NSCLC cell proliferation and invasion. In conclusion, the present study demonstrated that miRâ3120â5p promoted NSCLC progression by directly targeting KLF4.
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