https://eutils.ncbi.nlm.nih.gov/entrez/eutils/efetch.fcgi?db=pubmed&id=39128589&retmode=xml&tool=Litmetric&email=readroberts32@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09 391285892024102520241104
1873-29682292024NovBiochemical pharmacologyBiochem PharmacolThe 'ABC' of split-nanoluciferase HIF heterodimerization bioassays: Applications, Benefits & Considerations.11647811647810.1016/j.bcp.2024.116478S0006-2952(24)00461-1Hypoxia-inducible factors (HIF) are interesting targets for multiple therapeutic indications. While HIF activation is desired for the treatment of anemia-related and ischemic diseases, HIF inhibition is of tremendous interest to anti-cancer drug development. Different signaling events within the HIF pathway are being targeted by drug discovery programs, with a special interest in HIF-selective (possibly also HIF1/2 isoform-selective) compounds. In this study, we applied recently developed cell-based split-nanoluciferase HIF heterodimerization assays to study the effects of compounds, targeting HIF activity by various mechanisms of action. This study shows that the application of similar or diverse assay protocols allows to detect various influences on HIF heterodimerization as a key signaling event in the oxygen sensing pathway: increased HIF heterodimerization (roxadustat, MG-132), decreased HIF heterodimerization (PX-478, ibuprofen) and direct (HIF isoform-selective) heterodimerization inhibiting effects (PT-2385). Changes in treatment time and in the assay protocol allowed to assess direct and indirect effects on HIFα-HIFβ heterodimerization. In addition to the evaluation of applications of these new bioassays regarding pharmacological characterizations, benefits and considerations are discussed related to the use of cellular, luminescent-based bioassays. Briefly, benefits include the bidirectional nature of the biological readout, the upstream mechanism of detection, the differentiation between HIF1 and HIF2 effects and the simulation of various conditions. Specific and general considerations include cell-based, technical and disease/drug-related aspects (e.g., non-specific effects, color interference). In summary, the versatility of these bioassays offers benefits in widespread applications regarding drug discovery and pharmacological characterization of various therapeutics, applying either the same or optimized experimental protocols.Copyright © 2024 Elsevier Inc. All rights reserved.JanssensLiesl KLKLaboratory of Toxicology, Department of Bioanalysis, Faculty of Pharmaceutical Sciences, Ghent University, 9000 Ghent, Belgium.StoveChristophe PCPLaboratory of Toxicology, Department of Bioanalysis, Faculty of Pharmaceutical Sciences, Ghent University, 9000 Ghent, Belgium. Electronic address: christophe.stove@ugent.be.engJournal ArticleResearch Support, Non-U.S. Gov't20240810
EnglandBiochem Pharmacol01010320006-295202-amino-3-(4'-N,N-bis(2-chloroethyl)amino)phenylpropionic acid N-oxide138391-32-9Aryl Hydrocarbon Receptor Nuclear Translocator0Basic Helix-Loop-Helix Transcription Factors1B37H0967Pendothelial PAS domain-containing protein 10HIF1A protein, human0Hypoxia-Inducible Factor 1, alpha Subunit0IsoquinolinesEC 1.13.12.-Luciferases0Mustard Compounds0PhenylpropionatesX3O30D9YMXroxadustat0Hypoxia-Inducible Factor 1IMHumansAryl Hydrocarbon Receptor Nuclear TranslocatormetabolismBasic Helix-Loop-Helix Transcription Factorsmetabolismantagonists & inhibitorsBiological AssaymethodsHypoxia-Inducible Factor 1, alpha Subunitmetabolismantagonists & inhibitorsIsoquinolinespharmacologychemistryLuciferasesmetabolismgeneticsMustard CompoundspharmacologyPhenylpropionatesProtein Multimerizationdrug effectsHypoxia-Inducible Factor 1metabolismAnemiaCancerDrug developmentFunctional assayHypoxia inducible factorLuminescenceDeclaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
2024492024710202488202410261921202481204120248111917ppublish3912858910.1016/j.bcp.2024.116478S0006-2952(24)00461-1