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O-GlcNAcylated c-Jun antagonizes ferroptosis via inhibiting GSH synthesis in liver cancer.
- Source :
-
Cellular Signalling . Nov2019, Vol. 63, pN.PAG-N.PAG. 1p. - Publication Year :
- 2019
-
Abstract
- Ferroptosis is a metabolism-related cell death. Stimulating ferroptosis in liver cancer cells is a strategy to treat liver cancer. However, how to eradicate liver cancer cells through ferroptosis and the obstacles to inducing ferroptosis in liver cancer remain unclear. Here, we observed that erastin suppressed the malignant phenotypes of liver cancer cells by inhibiting O-GlcNAcylation of c-Jun and further inhibited protein expression, transcription activity and nuclear accumulation of c-Jun. Overexpression of c-Jun-WT with simultaneous PuGNAc treatment conversely inhibited erastin-induced ferroptosis, whereas overexpression of c-Jun-WT alone or overexpression of c-Jun-S73A (a non-O-GlcNAcylated form of c-Jun) with PuGNAc treatment did not exert a similar effect. GSH downregulation induced by erastin was restored by overexpression of c-Jun-WT with simultaneous PuGNAc treatment. In addition, overexpression of c-Jun-WT, but not its S73A mutant, induced PSAT1 and CBS transcription via directly binding to their promoter regions, suggesting that GSH synthesis is regulated by O-GlcNAcylated c-Jun. A positive correlation between c-Jun O-GlcNAcylation and GSH was observed in clinical samples. Collectively, O-GlcNAcylated c-Jun represents an obstructive factor to ferroptosis, and targeting O-GlcNAcylated c-Jun might be helpful for treating liver cancer. • Overexpression of c-Jun with simultaneous PuGNAc treatment inhibited ferroptosis. • Erastin-induced GSH downregulation was restored by O-GlcNAcylated c-Jun. • c-Jun stimulated PSAT1 and CBS transcription via binding to their promoter. • A positive correlation between c-Jun O-GlcNAcylation and GSH was observed. [ABSTRACT FROM AUTHOR]
- Subjects :
- *LIVER cancer
*LIVER cells
*CANCER cells
*CELL death
*PROTEIN expression
Subjects
Details
- Language :
- English
- ISSN :
- 08986568
- Volume :
- 63
- Database :
- Academic Search Index
- Journal :
- Cellular Signalling
- Publication Type :
- Academic Journal
- Accession number :
- 138292652
- Full Text :
- https://doi.org/10.1016/j.cellsig.2019.109384