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Success Stories


Publications
Yeast as a system for modeling mitochondrial disease mechanisms and discovering therapies

Disease Models & Mechanisms

Lasserre J, Dautant A, Aiyar RS, Kucharczyk R, Glatigny A, Tribouillard-Tanvier D, Rytka J, Blondel M, Skoczen N, Reynier P, Pitayu L, Rotig A, Delahodde A, Steinmetz LM, Dujardin G, Procaccio V, di Rago J
Disease Models & Mechanisms - vol. 8 509-526 (2015)

Mitochondrial diseases are severe and largely untreatable. Owing to the many essential processes carried out by mitochondria and the complex cellular systems that support these processes, these diseases are diverse, pleiotropic, and challenging to study. Much of our current understanding of mitochondrial function and dysfunction comes from studies in the baker’s yeast Saccharomyces cerevisiae. Because […]

Publications
A role for fragment-based drug design in developing novel lead compounds for central nervous system targets

Frontiers in Neurology

Wasko MJ, Pellegrene KA, Madura JD, Surratt CK
Frontiers in Neurology - vol. 6 1-11 (2015)

Hundreds of millions of U.S. dollars are invested in the research and development of a single drug. Lead compound development is an area ripe for new design strategies. Therapeutic lead candidates have been traditionally found using high-throughput in vitro pharmacological screening, a costly method for assaying thousands of compounds. This approach has recently been augmented […]

Publications
Efficient Generation of Cardiac Purkinje Cells from ESCs by Activating cAMP Signaling

Stem Cell Reports

Tsai SY, Maass K, Lu J, Fishman GI, Chen S, Evans T
Stem Cell Reports - vol. 4 1089-1102 (2015)

Dysfunction of the specialized cardiac conduction system (CCS) is associated with life-threatening arrhythmias. Strategies to derive CCS cells, including rare Purkinje cells (PCs), would facilitate models for mechanistic studies and drug discovery and also provide new cellular materials for regenerative therapies. A high-throughput chemical screen using CCS:lacz and Contactin2:egfp (Cntn2:egfp) reporter embryonic stem cell (ESC) […]

Publications
A Multiplexed Cell-Based Assay for the Identification of Modulators of Pre-Membrane Processing as a Target against Dengue Virus.

Journal of biomolecular screening

Stolp ZD, Smurthwaite CA, Reed C, Williams W, Dharmawan A, Djaballah H, Wolkowicz R
Journal of biomolecular screening - vol. 20 616-26 (2015)

The DenV pre-membrane protein (prM) is a crucial chaperone for the viral envelope protein, preventing premature fusion with vesicles during viral export. prM molecules in immature particles are cleaved by host proteases, leading to mature fusogenic virions. Blockade of prM cleavage would restrict fusion and represents a novel druggable opportunity against DenV. We have thus […]

Publications
Apoptosis induced by NAD depletion is inhibited by KN-93 in a CaMKII-independent manner.

Experimental cell research

Takeuchi M, Yamamoto T
Experimental cell research - vol. 335 62-67 (2015)

Nicotinamide phosphoribosyltransferase (NAMPT) is a key enzyme that catalyzes the synthesis of nicotinamide mononucleotide from nicotinamide (Nam) in the salvage pathway of mammalian NAD biosynthesis. Several potent NAMPT inhibitors have been identified and used to investigate the role of intracellular NAD and to develop therapeutics. NAD depletion induced by NAMPT inhibitors depolarizes mitochondrial membrane potential […]

Publications
Lansoprazole is an antituberculous prodrug targeting cytochrome bc1.

Nature communications

Rybniker J, Vocat A, Sala C, Busso P, Pojer F, Benjak A, Cole ST
Nature communications - vol. 6 1-8 (2015)

Better antibiotics capable of killing multi-drug-resistant Mycobacterium tuberculosis are urgently needed. Despite extensive drug discovery efforts, only a few promising candidates are on the horizon and alternative screening protocols are required. Here, by testing a panel of FDA-approved drugs in a host cell-based assay, we show that the blockbuster drug lansoprazole (Prevacid), a gastric proton-pump […]

Publications
Serotonergic signalling suppresses ataxin 3 aggregation and neurotoxicity in animal models of Machado-Joseph disease

Brain

Teixeira-Castro A, Jalles A, Esteves S, Kang S, Da Silva Santos L, Silva-Fernandes A, Neto MF, Brielmann RM, Bessa C, Duarte-Silva S, Miranda A, Oliveira S, Neves-Carvalho A, Bessa J, Summavielle T, Silverman RB, Oliveira P, Morimoto RI, Maciel P
Brain - vol. 138 3221-3237 (2015)

Polyglutamine diseases are a class of dominantly inherited neurodegenerative disorders for which there is no effective treatment. Here we provide evidence that activation of serotonergic signalling is beneficial in animal models of Machado-Joseph disease. We identified citalopram, a selective serotonin reuptake inhibitor, in a small molecule screen of FDA-approved drugs that rescued neuronal dysfunction and […]

Publications
Anticancer activity of pyrithione zinc in oral cancer cells identified in small molecule screens and xenograft model: Implications for oral cancer therapy

Molecular Oncology

Srivastava G, Matta A, Fu G, Somasundaram RT, Datti A, Walfish PG, Ralhan R
Molecular Oncology - vol. 9 1720-1735 (2015)

Oral squamous cell carcinoma (OSCC) patients diagnosed in late stages have limited chemotherapeutic options, underscoring the great need for development of new anticancer agents for more effective disease management. We aimed to identify novel anticancer agents for OSCC using quantitative high throughput assays for screening six chemical libraries consisting of 5170 small molecule inhibitors. In […]

Publications
Perhexiline promotes HER3 ablation through receptor internalization and inhibits tumor growth.

Breast cancer research

Ren X, Wang J, Osada T, Mook RA, Morse MA, Barak LS, Lyerly HK, Chen W
Breast cancer research - vol. 17 1-11 (2015)

INTRODUCTION: Human epidermal growth factor receptor HER3 has been implicated in promoting the aggressiveness and metastatic potential of breast cancer. Upregulation of HER3 has been found to be a major mechanism underlying drug resistance to EGFR and HER2 tyrosine kinase inhibitors and to endocrine therapy in the treatment of breast cancer. Thus, agents that reduce […]

Publications
Automation of a Phospho-STAT5 Staining Procedure for Flow Cytometry for Application in Drug Discovery

Journal of Biomolecular Screening

Malergue F, van Agthoven A, Scifo C, Egan D, Strous GJ
Journal of Biomolecular Screening - vol. 20 416-421 (2015)

Drug discovery often requires the screening of compound libraries on tissue cultured cells. Some major targets in drug discovery belong to signal transduction pathways, and PerFix EXPOSE* allows easy flow cytometry phospho assays. We thus investigated the possibility to further simplify and automate this assay, to allow the direct screening of drugs targeting signaling pathways. […]