The present study was undertaken to study the function of miRNA-199-3p in the regulation of human
lung cancer growth and
metastasis. The results showed significant (P < 0.05) downregulation of miRNA-199-3p in
lung cancer tissues and cell lines. Overexpression of miR-197 caused considerable inhibition of the viability and colony formation of the
lung cancer cells. The inhibition of proliferation was found to be due to the arrest of the SK-LU-1
lung cancer cells. At the G2/M phase of the cell cycle. In silico analysis and subsequent the dual-
luciferase assays showed that miR-199-3p targets Sp1 at molecular. The expression of Sp1 was significantly (P < 0.05) upregulated in
lung cancer cells and tissues. Nonetheless, miR-199-3p overexpression could cause post-transcriptional suppression of Sp1. Silencing of Sp1suppress the proliferation of SK-LU-1
lung cancer cells. However, overexpression
Sp1 transcription factor prevents the
tumor-suppressive effects of miR-199-3p on
lung cancer cells. Additionally, miR-199-3p was found to suppresses the migration, invasion and epithelial-to-mesenchymal transition of human
lung cancer cells. Summing up,
miRNA-199-3p/SP1 axis controls the growth and
metastasis of SK-LU-1
lung cancer cells.