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Development of a 3D Tissue Culture-Based High-Content Screening Platform That Uses Phenotypic Profiling to Discriminate Selective Inhibitors of Receptor Tyrosine Kinases.

Title: Development of a 3D Tissue Culture-Based High-Content Screening Platform That Uses Phenotypic Profiling to Discriminate Selective Inhibitors of Receptor Tyrosine Kinases.
Authors: Booij TH; Klop MJ; Yan K; Szantai-Kis C; Szokol Bálint; Őrfi László; Kéri György; van de Water B; Price LS
Contributors: SE/GYTK/Gyógyszerészi Kémiai Intézet; SE/AOK/I/OVMBPI/MTA-SE Pathobiokémiai Kutatócsoport; Semmelweis Egyetem
Publication Year: 2016
Collection: Semmelweis Egyetem: Repozitórium
Description: 3D tissue cultures provide a more physiologically relevant context for the screening of compounds, compared with 2D cell cultures. Cells cultured in 3D hydrogels also show complex phenotypes, increasing the scope for phenotypic profiling. Here we describe a high-content screening platform that uses invasive human prostate cancer cells cultured in 3D in standard 384-well assay plates to study the activity of potential therapeutic small molecules and antibody biologics. Image analysis tools were developed to process 3D image data to measure over 800 phenotypic parameters. Multiparametric analysis was used to evaluate the effect of compounds on tissue morphology. We applied this screening platform to measure the activity and selectivity of inhibitors of the c-Met and epidermal growth factor (EGF) receptor (EGFR) tyrosine kinases in 3D cultured prostate carcinoma cells. c-Met and EGFR activity was quantified based on the phenotypic profiles induced by their respective ligands, hepatocyte growth factor and EGF. The screening method was applied to a novel collection of 80 putative inhibitors of c-Met and EGFR. Compounds were identified that induced phenotypic profiles indicative of selective inhibition of c-Met, EGFR, or bispecific inhibition of both targets. In conclusion, we describe a fully scalable high-content screening platform that uses phenotypic profiling to discriminate selective and nonselective (off-target) inhibitors in a physiologically relevant 3D cell culture setting.
Document Type: article in journal/newspaper
Language: English
ISSN: 1087-0571
Relation: urn:issn:1087-0571; http://repo.lib.semmelweis.hu//handle/123456789/5308; 3169835; 000384469400004
DOI: 10.1177/1087057116657269
Availability: http://repo.lib.semmelweis.hu//handle/123456789/5308; https://doi.org/10.1177/1087057116657269
Accession Number: edsbas.ED2EA3CE
Database: BASE