Activation of Transcription Factor Nrf2 in HeLa Cells under the Action of Nitrosyl Iron Complex with N-Ethylthiourea

Bull Exp Biol Med. 2024 Mar;176(5):562-566. doi: 10.1007/s10517-024-06067-2. Epub 2024 May 9.

Abstract

We studied the effect of an NO donor, nitrosyl iron complex with N-ethylthiourea, on Nrf2-dependent antioxidant system activation of tumor cells in vitro. The complex increased intracellular accumulation of Nrf2 transcription factor and induced its nuclear translocation. It was shown that both heme oxygenase-1 gene and protein expression increased significantly under the influence of the complex. Nrf2 activation was accompanied by a decrease in the intracellular accumulation of proinflammatory transcription factor NF-κB p65 subunit and expression of its target genes. The cytotoxic effect of N-ethylthiourea leads to induction of Nrf2/HO-1 antioxidant response and suppression of NF-κB-dependent processes in tumor cells.

Keywords: Nrf2; heme oxygenase; iron nitrosyl complexes; nitrogen monoxide.

MeSH terms

  • Antioxidants / pharmacology
  • HeLa Cells
  • Heme Oxygenase-1* / genetics
  • Heme Oxygenase-1* / metabolism
  • Humans
  • Iron* / metabolism
  • NF-E2-Related Factor 2* / genetics
  • NF-E2-Related Factor 2* / metabolism
  • Nitrogen Oxides / metabolism
  • Nitrogen Oxides / pharmacology
  • Thiourea* / analogs & derivatives
  • Thiourea* / pharmacology
  • Transcription Factor RelA / genetics
  • Transcription Factor RelA / metabolism

Substances

  • NFE2L2 protein, human
  • dinitrosyl iron complex
  • HMOX1 protein, human