Ginsenoside Rh2 inhibits HeLa cell energy metabolism and induces apoptosis by upregulating voltage‑dependent anion channel 1

Int J Mol Med. 2020 Nov;46(5):1695-1706. doi: 10.3892/ijmm.2020.4725. Epub 2020 Sep 14.

Abstract

20(S)‑Ginsenoside Rh2 [20(S)‑GRh2], one of the main active components of Panax ginseng, induces apoptosis in a wide range of cancer cell types. The present study found that 20(S)‑GRh2 reduces mitochondrial membrane potential, decreases adenosine triphosphate generation and induces reactive oxygen species in HeLa cervical cancer cells. In addition, 20(S)‑GRh2 activated mitochondrion‑dependent apoptosis and inhibited both mitochondrial oxidative phosphorylation and glycolysis in HeLa cells. It was found that voltage‑dependent anion channel 1 (VDAC1) expression was significantly upregulated by 20(S)‑GRh2 treatment, while hexokinase 2 expression was downregulated and segregated from the mitochondria. Furthermore, 20(S)‑GRh2 promoted Bax transport from the cytoplasm to the mitochondria, and knockdown of VDAC1 inhibited Bax transport and apoptosis. These results suggest that VDAC1 is a novel target of 20(S)‑GRh2. The present study provides a better understanding of the mechanistic link between cervical cancer metabolism and growth control, and these results may facilitate the development of new treatments for cervical cancer.

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Apoptosis / drug effects*
  • Cell Respiration / drug effects
  • Cell Survival / drug effects
  • Energy Metabolism / drug effects*
  • Ginsenosides / chemistry
  • Ginsenosides / pharmacology*
  • Glycolysis / drug effects
  • HeLa Cells
  • Hexokinase / metabolism
  • Humans
  • Membrane Potential, Mitochondrial / drug effects
  • Models, Biological
  • Oxidative Phosphorylation / drug effects
  • Reactive Oxygen Species / metabolism
  • Stress, Physiological / drug effects
  • Up-Regulation / drug effects
  • Up-Regulation / genetics*
  • Voltage-Dependent Anion Channel 1 / genetics*
  • Voltage-Dependent Anion Channel 1 / metabolism
  • bcl-2-Associated X Protein / metabolism

Substances

  • Ginsenosides
  • Reactive Oxygen Species
  • bcl-2-Associated X Protein
  • ginsenoside Rh2
  • Adenosine Triphosphate
  • Voltage-Dependent Anion Channel 1
  • Hexokinase