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Vesnarinone suppresses TNFα mRNA expression by inhibiting valosin-containing protein.
- Source :
-
Molecular pharmacology [Mol Pharmacol] 2013 May; Vol. 83 (5), pp. 930-8. Date of Electronic Publication: 2013 Feb 07. - Publication Year :
- 2013
-
Abstract
- Vesnarinone is a synthetic quinolinone derivative used in the treatment of cardiac failure and cancer. It is also known to cause agranulocytosis as a side effect, which restricts its use, although the mechanism underlying agranulocytosis is not well understood. Here, we show that vesnarinone binds to valosin-containing protein (VCP), which interacts with polyubiquitinated proteins and is essential for the degradation of IκBα to activate nuclear factor (NF)κB. We show that vesnarinone impairs the degradation of IκBα, and that the impairment of the degradation of IκBα is the result of the inhibition of the interaction between VCP and the 26S proteasome by vesnarinone. These results suggest that vesnarinone suppresses NFκB activation by inhibiting the VCP-dependent degradation of polyubiquitinated IκBα, resulting in the suppression of tumor necrosis factor-α mRNA expression.
- Subjects :
- Adenosine Triphosphatases genetics
Adenosine Triphosphatases metabolism
Cell Cycle Proteins genetics
Cell Cycle Proteins metabolism
Cell Line
HEK293 Cells
Humans
I-kappa B Proteins genetics
I-kappa B Proteins metabolism
NF-KappaB Inhibitor alpha
NF-kappa B genetics
NF-kappa B metabolism
Proteasome Endopeptidase Complex genetics
Proteasome Endopeptidase Complex metabolism
Pyrazines
RNA, Messenger genetics
Tumor Necrosis Factor-alpha metabolism
Valosin Containing Protein
Adenosine Triphosphatases antagonists & inhibitors
Cell Cycle Proteins antagonists & inhibitors
Quinolines pharmacology
RNA, Messenger antagonists & inhibitors
RNA, Messenger biosynthesis
Tumor Necrosis Factor-alpha genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1521-0111
- Volume :
- 83
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Molecular pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 23393163
- Full Text :
- https://doi.org/10.1124/mol.112.081935