Spica Prunellae extract suppresses the growth of human colon carcinoma cells by targeting multiple oncogenes via activating miR-34a

Oncol Rep. 2017 Sep;38(3):1895-1901. doi: 10.3892/or.2017.5792. Epub 2017 Jul 6.

Abstract

Spica Prunellae is the spike of the herb Prunella vulgaris L. in traditional Chinese medicine which is often used for the treatment of various cancers including colorectal cancer. In the present study, we found that a key tumor suppressor, microRNA-34a (miR-34a) is involved in the antitumor activity for Spica Prunellae. Human colon carcinoma HCT-8 cells treated with an ethanol extract of Spica Prunellae (EESP) had significantly decreased cell proliferation and viability, in a dose-dependent manner. Flow cytometry analysis with Annexin V/PI staining analysis revealed that EESP treatment could induce apoptosis of HCT-8 cells. The level of miR-34a was upregulated in HCT-8 cells following EESP treatment, whereas expression levels of its target genes Notch1, Notch2 and Bcl-2 were downregulated. Inhibition of miR-34a rescued the expression of these target genes. These results revealed that Spica Prunellae can suppress the growth of HCT-8 cells by targeting Notch1, Notch2 and Bcl-2 via activation of miR-34a.

MeSH terms

  • Apoptosis / drug effects
  • Apoptosis / genetics
  • Carcinoma / drug therapy*
  • Carcinoma / metabolism
  • Cell Line, Tumor
  • Cell Proliferation / drug effects*
  • Cell Proliferation / genetics
  • Colonic Neoplasms / drug therapy*
  • Colonic Neoplasms / metabolism
  • Down-Regulation / drug effects
  • Down-Regulation / genetics
  • Gene Expression Regulation, Neoplastic / drug effects
  • Gene Expression Regulation, Neoplastic / genetics
  • Humans
  • MicroRNAs / genetics*
  • Oncogenes / genetics*
  • Plant Extracts / pharmacology*
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Prunella / chemistry*
  • Receptor, Notch1 / genetics
  • Receptor, Notch2 / genetics
  • Up-Regulation / drug effects
  • Up-Regulation / genetics

Substances

  • MIRN34 microRNA, human
  • MicroRNAs
  • Plant Extracts
  • Proto-Oncogene Proteins c-bcl-2
  • Receptor, Notch1
  • Receptor, Notch2