0000000000267242

AUTHOR

Ernst Urban

showing 2 related works from this author

Identification of new P-glycoprotein inhibitors derived from cardiotonic steroids

2014

P-glycoprotein (ABCB1, MDR1) is capable of extruding chemotherapeutics outside the cell and its overexpression in certain cancer cells may cause failure of chemotherapy. Many attempts were carried out to identify potent inhibitors of this transporter and numerous compounds were shown to exert inhibitory effects in vitro, but so far none were able to make their way to the clinic due to serious complications. Natural compounds represent a great source of therapeutics, which are believed to be safe and effective. Therefore, we have screened a large library of naturally occurring cardiotonic steroids and their derivatives using high throughput flow cytometry. We were able to identify six compou…

Cell SurvivalHigh-throughput screeningIn silicoPharmacologyBiochemistryProtein Structure SecondaryCell LineFlow cytometryCardiac Glycosideschemistry.chemical_compoundmedicineHumansATP Binding Cassette Transporter Subfamily B Member 1P-glycoproteinPharmacologyDose-Response Relationship Drugbiologymedicine.diagnostic_testResazurinmedicine.diseaseIn vitroProtein Structure TertiaryLeukemiachemistryDoxorubicinCancer cellbiology.proteinBiochemical Pharmacology
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Cytotoxicity of cardiotonic steroids in sensitive and multidrug-resistant leukemia cells and the link with Na(+)/K(+)-ATPase.

2015

Cardiotonic steroids have long been in clinical use for treatment of heart failure and are now emerging as promising agents in various diseases, especially cancer. Their main target is Na(+)/K(+)-ATPase, a membrane protein involved in cellular ion homeostasis. Na(+)/K(+)-ATPase has been implicated in cancer biology by affecting several cellular events and signaling pathways in both sensitive and drug-resistant cancer cells. Hence, we investigated the cytotoxic activities of 66 cardiotonic steroids and cardiotonic steroid derivatives in sensitive CCRF-CEM and multidrug-resistant CEM/ADR5000 leukemia cells. Data were then subjected to quantitative structure-activity relationship analysis (QSA…

DigoxinCell SurvivalEndocrinology Diabetes and MetabolismClinical BiochemistryPrimary Cell CultureGene ExpressionQuantitative Structure-Activity RelationshipAntineoplastic AgentsBiologyPharmacologyBiochemistryCardiac GlycosidesEndocrinologyCellular ion homeostasisCell Line TumorCytotoxic T cellHumansNa+/K+-ATPaseCytotoxicityMolecular BiologyCell BiologyMolecular biologyDrug Resistance MultipleBlotBufanolidesMolecular Docking SimulationVerapamilCell cultureDoxorubicinDrug Resistance NeoplasmCancer cellLeukocytes MononuclearMolecular MedicineSignal transductionSodium-Potassium-Exchanging ATPaseSignal TransductionThe Journal of steroid biochemistry and molecular biology
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