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pmid:33350095
Exosomal miR-3180-3p inhibits proliferation and metastasis of non-small cell lung cancer by downregulating FOXP4.
Tengfei Chen · Yali Liu · Jun Chen · Huifei Zheng · Qiuyun Chen · Jun Zhao
Thoracic cancer · 2021 doi:10.1111/1759-7714.13759
Paper
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Experiment
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Data
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Analysis
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Execution
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Complete file
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In this study, we explored the functions and mechanisms of exosomes transferring miR-3180-3p in NSCLC progression.\nMETHODS: The expression levels of miR-3180-3p in NSCLC tissues and paracarcinoma tissues was obtained from the GEO database (GEO: GSE53882). Exosomes derived from A549 cells were identified. Proliferation, migration and invasion were measured after treatment with exosomal miR-3180-3p or transfection using miR-3180-3p mimics. The relationship between miR-3180-3p and forkhead box P4 (FOXP4) was predicted using a bioinformatic tool and measured using a dual-luciferase reporter gene assay and western blotting. Finally, a mouse xenograft model of NSCLC cells was established to verify the function of exosomal miR-3180-3p in vivo.\nRESULTS: We found that miR-3180-3p decreased in both NSCLC cell lines and patient tissues. Overexpression of miR-3180-3p or treatment with exosomal miR-3180-3p significantly suppressed cell proliferation and metastasis in NSCLC cell lines. Subsequently, we found miR-3180-3p downregulated FOXP4 protein expression levels. Furthermore, the volumes and weights of nude mouse tumors expressing exosomal miR-3180-3p were significantly reduced.\nCONCLUSIONS: Exosomal miR-3180-3p suppresses NSCLC progression by downregulating FOXP4 expression.\nKEY POINTS: SIGNIFICANT FINDINGS OF THE STUDY: We found that exosomal miR-3180-3p suppressed NSCLC progression and also identified a miR-3180-3p target gene. 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