<<< Full experiment listing

PXD031319

PXD031319 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleNovel assays monitoring direct GR protein activity exhibit high predictive power for ligand activity on endogenous GR gene targets
DescriptionExogenous glucocorticoids are widely used in the clinic for the treatment of inflammatory disorders and auto-immune diseases. Unfortunately, their use is hampered by many side effects and therapy resistance. Efforts to find more selective glucocorticoid receptor (GR) agonists and modulators (called SEGRAMs), able to separate anti-inflammatory effects via gene suppression from metabolic effects via gene activation, have been unsuccessful so far. In this study, we characterized a set of functionally diverse GR ligands in A549 cells, first using a panel of luciferase-based reporter gene assays evaluating GR-driven gene activation and gene suppression. We expanded this minimal assay set with novel luciferase-based read-outs monitoring GR protein levels, GR dimerization and GR Serine 211 (Ser211) phosphorylation status and compared their outcomes with compound effects on the mRNA levels of known GR target genes in A549 cells and primary hepatocytes. We found that luciferase reporters evaluating GR-driven gene activation and gene repression were not always reliable predictors for effects on endogenous target genes. Remarkably, our novel assay monitoring GR Ser211 phosphorylation levels proved to be the most reliable predictor for compound effects on almost all tested endogenous GR targets, both driven by gene activation and repression. The integration of this novel assay in existing screening platforms may therefore increase chances to find novel GR ligands with an improved therapeutic benefit.
HostingRepositoryPRIDE
AnnounceDate2022-04-11
AnnouncementXMLSubmission_2022-04-10_16:50:27.512.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterDelphi Van Haver
SpeciesList scientific name: Homo sapiens (Human); NCBI TaxID: 9606;
ModificationListacetylated residue; monohydroxylated residue; iodoacetamide derivatized residue
InstrumentOrbitrap Fusion Lumos
Dataset History
RevisionDatetimeStatusChangeLog Entry
02022-01-30 10:47:02ID requested
12022-04-10 16:50:27announced
Publication List
Dataset with its publication pending
Keyword List
submitter keyword: Glucocorticoids, glucocorticoid receptor, SEGRAM, drug discovery, inflammation, assay development
Contact List
Kris Gevaert
contact affiliationVIB Center for Medical Biotechnology (CMB), Ghent, Belgium Department of Biomolecular Medicine, Ghent University, Ghent, Belgium
contact emailkris.gevaert@vib-ugent.be
lab head
Delphi Van Haver
contact affiliationVIB Proteomics Core
contact emaildelphi.vanhaver@vib-ugent.be
dataset submitter
Full Dataset Link List
Dataset FTP location
NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2022/04/PXD031319
PRIDE project URI
Repository Record List
[ + ]