| Literature DB >> 24799995 |
Preetpal S Sidhu1, Nicholas Nassif1, Megan M McCallum1, Kelly Teske1, Belaynesh Feleke1, Nina Y Yuan1, Premchendar Nandhikonda1, James M Cook1, Rakesh K Singh2, Daniel D Bikle3, Leggy A Arnold1.
Abstract
Nuclear receptor coregulators are master regulators of transcription and selectively interact with the vitamin D receptor (VDR) to modulate cell differentiation, cell proliferation and calcium homeostasis. Herein, we report the syntheses and evaluation of highly potent and selective VDR-coactivator inhibitors based on a recently identified 3-indolylmethanamine scaffold. The most active compound, PS121912, selectively inhibited VDR-mediated transcription among eight other nuclear receptors tested. PS121912 is also selectively disrupting the binding between VDR and the third nuclear receptor interaction domain of the coactivator SRC2. Genetic studies revealed that PS121912 behaves like a VDR antagonist by repressing 1,25-(OH)2D3 activated gene transcription. In addition, PS121912 induced apoptosis in HL-60.Entities:
Keywords: 3-indolylmethanamines; CAMP; CYP24A1; HL60; VDR; Vitamin D receptor; apoptosis; fluorescence polarization; high throughput screening; steroid receptor coactivator
Year: 2014 PMID: 24799995 PMCID: PMC4007349 DOI: 10.1021/ml400462j
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345