Gene interactions and pathways from curated databases and text-mining

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NCOR1 — VDR

Protein-Protein interactions - manually collected from original source literature:

Studies that report less than 10 interactions are marked with *

Text-mined interactions from Literome

Herdick et al., J Mol Biol 2000 : This study demonstrates that the interaction of the VDR with NCoR results in a preferential stabilization of the VDR in a non-agonistic conformation ( silent state ), whereas within a complex with SRC-1 VDR is in its agonistic conformation ( activated state )
Banwell et al., J Steroid Biochem Mol Biol 2004 (Breast Neoplasms) : Proliferation of the non-malignant breast epithelial cell line, MCF-12A, is sensitively and completely inhibited by 1alpha,25-dihydroxyvitamin D ( 3 ) ( 1alpha,25 ( OH ) ( 2 ) D ( 3 ) ) ( ED90 = 70 nM ), We used real time RT-PCR to demonstrate that the relative resistance to 1alpha,25 ( OH ) ( 2 ) D ( 3 ) of MDA-MB-231 cells ( ED50 > 100 nM ) correlated with significantly reduced Vitamin D receptor (VDR) and increased NCoR1 nuclear receptor co-repressor mRNA ( 0.1-fold reduction in VDR and 1.7-fold increase in NCoR1 relative to MCF-12A ( P < 0.05 ) )
Banwell et al., Clin Cancer Res 2006 (Breast Neoplasms) : Altered nuclear receptor corepressor expression attenuates vitamin D receptor signaling in breast cancer cells