miR-593-5p inhibit cell proliferation by targeting PLK1 in non small cell lung cancer cells

Pathol Res Pract. 2020 Feb;216(2):152786. doi: 10.1016/j.prp.2019.152786. Epub 2019 Dec 13.

Abstract

Worldwide, lung cancer has the highest rates of mortality and morbidity, with the majority of its pathology attributable to non-small cell lung cancer (NSCLC). MicroRNAs are pivotal in the occurrence and development of cancer. However, the role of miRNA-593-5p in the progression of NSCLC is not clear. In this study, we investigate, in vitro, whether miRNA-593-5p inhibits NSCLC cell proliferation. To clarify its specific mechanism of inhibition, we used bioinformatics to predict its target genes and identified PLK1. Luciferase reporter assay confirmed the binding of miR-593-5p to the PLK1 3'-UTR in a sequence-specific manner in NSCLC cells. Additionally, we also found through Western blot and quantitative RT-PCR that miR-593-5p down-regulates the expression of PLK1 protein. Finally, PLK1 overexpression was shown to disinhibit NSCLC cell proliferation. Taken together, this evidence suggests that miR-593-5p inhibits NSCLC cell proliferation by inhibiting PLK1 expression.

Keywords: PLK1; miR-593-5p; non-small cell lung cancer cells.

MeSH terms

  • Carcinoma, Non-Small-Cell Lung / genetics*
  • Carcinoma, Non-Small-Cell Lung / pathology
  • Cell Cycle Proteins / genetics*
  • Cell Line, Tumor
  • Cell Proliferation / genetics
  • Computational Biology
  • Down-Regulation
  • Gene Expression Regulation, Neoplastic / genetics*
  • Genes, Reporter
  • Humans
  • Lung Neoplasms / genetics*
  • Lung Neoplasms / pathology
  • MicroRNAs / genetics*
  • Polo-Like Kinase 1
  • Protein Serine-Threonine Kinases / genetics*
  • Proto-Oncogene Proteins / genetics*
  • RNA Interference

Substances

  • Cell Cycle Proteins
  • MIRN593 microRNA, human
  • MicroRNAs
  • Proto-Oncogene Proteins
  • Protein Serine-Threonine Kinases