C4‐2B cells were treated for 24 h with PX‐478 (Selleck Chemicals; catalog No.S7612) at 50 μM and/or with enzalutamide (MDV3100; Selleckchem; catalog No.S1250) at 10, 25 and 50 μM, or vehicle (DMSO). DU‐145 and PC‐3 cells were treated for 24 h with PX‐478 at 50 μM.
Prostate Organoids Treated with Enzalutamide
C4‐2B cells were treated for 24 h with PX‐478 (Selleck Chemicals; catalog No.S7612) at 50 μM and/or with enzalutamide (MDV3100; Selleckchem; catalog No.S1250) at 10, 25 and 50 μM, or vehicle (DMSO). DU‐145 and PC‐3 cells were treated for 24 h with PX‐478 at 50 μM.
Corresponding Organization :
Other organizations : Institut de génétique et de biologie moléculaire et cellulaire, Centre National de la Recherche Scientifique, Inserm, Université de Strasbourg, German Center for Diabetes Research, Heinrich Heine University Düsseldorf, Deutsches Diabetes-Zentrum e.V.
Variable analysis
- Enzalutamide (MDV3100) treatment at 25 and 50 μM
- PX-478 treatment at 50 μM
- Cellular responses in Pten(i)pe-/- and Pten/Hif1a(i)pe-/- prostate organoid cultures
- Cellular responses in C4-2B, DU-145, and PC-3 cell lines
- Vehicle (DMSO) treatment
- Mycoplasma-free but not recently authenticated cell lines
- Positive control: None explicitly mentioned
- Negative control: Vehicle (DMSO) treatment
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