Suppression of NRF2/ARE by convallatoxin sensitises A549 cells to 5-FU-mediated apoptosis

Free Radic Res. 2018 Dec;52(11-12):1416-1423. doi: 10.1080/10715762.2018.1489132. Epub 2018 Sep 10.

Abstract

NF-E2-related factor 2 (NRF2) regulates transcription of phase II cytoprotective enzymes to protect normal cells against oxidative stress. However, a high level of NRF2 offers a growth advantage, chemoresistance, and radioresistance in cancer. In the present study, we have identified convallatoxin as a novel inhibitor of NRF2/ARE. Suppression of NRF2 by convallatoxin was not transcriptionally mediated, but regulated at the level of proteolysis. Convallatoxin activated GSK-3β and suppression of NRF2 by convallatoxin required the Neh6 domain. Convallatoxin sensitised A549 cells to 5-fluorouracil-mediated cell death by promoting apoptosis. Together, our results provide evidence that convallatoxin might be useful as a chemotherapeutic adjuvant due to its ability to suppress NRF2/ARE.

Keywords: 5-Fluorouracil (5-FU); NRF2; antioxidant response element (ARE); convallatoxin.

MeSH terms

  • A549 Cells
  • Antioxidant Response Elements / drug effects*
  • Antioxidant Response Elements / genetics
  • Apoptosis / drug effects*
  • Dose-Response Relationship, Drug
  • Enzyme Inhibitors / pharmacology*
  • Fluorouracil / pharmacology*
  • Humans
  • Molecular Conformation
  • NF-E2-Related Factor 2 / antagonists & inhibitors*
  • Strophanthins / pharmacology*
  • Structure-Activity Relationship

Substances

  • Enzyme Inhibitors
  • NF-E2-Related Factor 2
  • NFE2L2 protein, human
  • Strophanthins
  • convallatoxin
  • Fluorouracil