Effects of Icaritin on the physiological activities of esophageal cancer stem cells

Biochem Biophys Res Commun. 2018 Oct 12;504(4):792-796. doi: 10.1016/j.bbrc.2018.08.060. Epub 2018 Sep 11.

Abstract

Icaritin is a compound extracted from herb, recent study have found it is able to influence the activity of various types of cancer. Our aim was to investigate the effects of Icaritin on the physiological activities of esophageal cancer stem cells (CSCs). In this study, esophageal cancer cells were cultured and CD133 positive esophageal CSCs were sorted by flow cytometry. Changes in the physiological activity of esophageal CSCs following treatment with different concentrations of Icaritin (0, 12.5, 25, 50, and 100 μmol/L) were evaluated. The CCK-8 method and Transwell assay were used to determine the effects of Icaritin on the proliferation, migration, and invasion of esophageal CSCs. Flow cytometery was used to investigate its effect on the apoptosis of CSCs. The effect of Icaritin on the expression of proteins in Wnt and Hedgehog signaling pathways were determined using western blot test. Consequently, Icaritin inhibited the proliferation, migration, and invasion of esophageal CSCs in a dose-dependent manner. It promoted cell apoptosis, and influenced the levels of proteins in Wnt and Hedgehog signaling pathways. It may act as a promising drug in the therapy of esophageal cancer.

Keywords: Cancer stem cell; Esophageal cancer; Icaritin; Signaling pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Apoptosis / drug effects
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Esophageal Neoplasms / drug therapy
  • Esophageal Neoplasms / metabolism
  • Esophageal Neoplasms / pathology*
  • Flavonoids / pharmacology*
  • Glycogen Synthase Kinase 3 beta / metabolism
  • Hedgehog Proteins / metabolism
  • Humans
  • Neoplastic Stem Cells / drug effects*
  • Neoplastic Stem Cells / metabolism*
  • Neoplastic Stem Cells / pathology
  • Smoothened Receptor / metabolism
  • Tumor Cells, Cultured
  • Wnt Signaling Pathway / drug effects
  • Zinc Finger Protein GLI1 / metabolism
  • beta Catenin / metabolism

Substances

  • Antineoplastic Agents, Phytogenic
  • CTNNB1 protein, human
  • Flavonoids
  • GLI1 protein, human
  • Hedgehog Proteins
  • SMO protein, human
  • Smoothened Receptor
  • Zinc Finger Protein GLI1
  • beta Catenin
  • GSK3B protein, human
  • Glycogen Synthase Kinase 3 beta
  • icaritin