Selective activation of cellular stress response pathways by fumaric acid esters

• Published in: FEBS open bio 2024-08, Vol.14 (8), p.1230-1246
• Main Authors: Erler, Katrin, Krafczyk, Niklas, Steinbrenner, Holger, Klotz, Lars‐Oliver
• Format: Article
• Language: English
• Subjects: AKT; alkylation; Antioxidants; Cell activation; Cell Line, Tumor; Cellular stress response; Collaboration; Dehydrogenases; Enzymes; Esters; Esters - metabolism; Esters - pharmacology; Forkhead protein; Forkhead Transcription Factors - metabolism; FOXO; Fumarates - metabolism; Fumarates - pharmacology; Fumaric acid; Gene expression; Glucose; Glutathione; Hep G2 Cells; Hepatoma; Humans; insulin signaling; Insuling Signalling; Kinases; NF-E2-Related Factor 2 - metabolism; NRF2; NRF2 protein; Oxidants; Oxidative Stress; Oxidative Stress - drug effects; Proteins; Psoriasis; Signal Transduction - drug effects; Solvents; Transcription activation; Transcription factors; Xenobiotics
• ISSN: 2211-5463; 2211-5463
• DOI: 10.1002/2211-5463.13833

The cellular response to oxidants or xenobiotics comprises two key pathways, resulting in modulation of NRF2 and FOXO transcription factors, respectively. Both mount a cytoprotective response, and their activation relies on crucial protein thiol moieties. Using fumaric acid esters (FAEs), known thiol‐reactive compounds, we tested for activation of NRF2 and FOXO pathways in cultured human hepatoma cells by dimethyl/diethyl as well as monomethyl/monoethyl fumarate. Whereas only the diesters caused acute glutathione depletion and activation of the stress kinase p38MAPK, all four FAEs stimulated NRF2 stabilization and upregulation of NRF2 target genes. However, no significant FAE‐induced activation of FOXO‐dependent target gene expression was observed. Therefore, while both NRF2 and FOXO pathways are responsive to oxidants and xenobiotics, FAEs selectively activate NRF2 signaling. NRF2 and FOXO transcription factors respond to oxidants and xenobiotics. We analyzed the activation of NRF2 and FOXO by fumaric acid esters in HepG2 cells. Whereas only the diesters caused acute glutathione depletion and activation of the stress kinase p38MAPK, all tested compounds stimulated NRF2 signaling. No FOXO‐dependent response was observed, indicating that FAEs selectively activate NRF2 signaling.