Cold Atmospheric Pressure Plasma-Activated Medium Induces Selective Cell Death in Human Hepatocellular Carcinoma Cells Independently of Singlet Oxygen, Hydrogen Peroxide, Nitric Oxide and Nitrite/Nitrate

Int J Mol Sci. 2021 May 24;22(11):5548. doi: 10.3390/ijms22115548.

Abstract

Cold atmospheric pressure plasma (CAP) and plasma-activated medium (PAM) induce cell death in diverse cancer cells and may function as powerful anti-cancer agents. The main components responsible for the selective anti-cancer effects of CAP and PAM remain elusive. CAP or PAM induces selective cell death in hepatocellular carcinoma cell lines Hep3B and Huh7 containing populations with cancer stem cell markers. Here, we investigated the major component(s) of CAP and PAM for mediating the selective anti-proliferative effect on Hep3B and Huh7 cells. The anti-proliferative effect of CAP was mediated through the medium; however, the reactive oxygen species scavenger N-acetyl cysteine did not suppress PAM-induced cell death. Neither high concentrations of nitrite or nitrite/nitrate nor a low concentration of H2O2 present in the PAM containing sodium pyruvate affected the viability of Hep3B and Huh7 cells. Inhibitors of singlet oxygen, superoxide anions, and nitric oxide retained the capacity of PAM to induce anti-cancer effects. The anti-cancer effect was largely blocked in the PAM prepared by placing an aluminum metal mesh, but not a dielectric PVC mesh, between the plasma source and the medium. Hence, singlet oxygen, hydrogen peroxide, nitric oxide, and nitrite/nitrate are not the main factors responsible for PAM-mediated selective death in Hep3B and Huh7 cells. Other factors, such as charged particles including various ions in CAP and PAM, may induce selective anti-cancer effects in certain cancer cells.

Keywords: charged particles; cold atmospheric pressure plasma (CAP); hepatocellular carcinoma cell lines Hep3B and Huh7; plasma-activated medium (PAM); reactive oxygen and nitrogen species (RONS).

MeSH terms

  • Acetylcysteine / pharmacology
  • Aluminum / pharmacology
  • Antineoplastic Agents / pharmacology*
  • Atmospheric Pressure
  • Carcinoma, Hepatocellular / drug therapy*
  • Carcinoma, Hepatocellular / metabolism
  • Cell Death / drug effects*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Free Radicals / metabolism*
  • Humans
  • Hydrogen Peroxide / pharmacology
  • Liver Neoplasms / drug therapy*
  • Liver Neoplasms / metabolism
  • Neoplastic Stem Cells / drug effects
  • Neoplastic Stem Cells / metabolism
  • Nitrates / pharmacology*
  • Nitric Oxide / metabolism
  • Nitrites / pharmacology*
  • Plasma Gases / pharmacology*
  • Reactive Nitrogen Species / metabolism
  • Reactive Oxygen Species / metabolism
  • Singlet Oxygen / metabolism

Substances

  • Antineoplastic Agents
  • Free Radicals
  • Nitrates
  • Nitrites
  • Plasma Gases
  • Reactive Nitrogen Species
  • Reactive Oxygen Species
  • Singlet Oxygen
  • Nitric Oxide
  • Hydrogen Peroxide
  • Aluminum
  • Acetylcysteine