◀ Back to AR
AR — HDAC1
Pathways - manually collected, often from reviews:
-
NCI Pathway Database Regulation of Androgen receptor activity:
T-DHT/AR/TIP60 complex (AR-KAT5)
→
HDAC1 (HDAC1)
(transcription, activates)
Brady et al., J Biol Chem 1999*, Gaughan et al., J Biol Chem 2001, Gaughan et al., J Biol Chem 2002*
Evidence: mutant phenotype, reporter gene, physical interaction
-
NCI Pathway Database Regulation of Androgen receptor activity:
AR/T-DHT complex (AR)
→
HDAC1 (HDAC1)
(proteasomal ubiquitin-dependent protein catabolic process, collaborate)
Gaughan et al., Nucleic Acids Res 2005*
Evidence: mutant phenotype, assay
Protein-Protein interactions - manually collected from original source literature:
Studies that report less than 10 interactions are marked with *
-
IRef Biogrid Interaction:
HDAC1
—
AR
(physical association, affinity chromatography technology)
Gaughan et al., Nucleic Acids Res 2005*
-
IRef Biogrid Interaction:
HDAC1
—
AR
(physical association, affinity chromatography technology)
Gobinet et al., Biochemistry 2005*
-
IRef Biogrid Interaction:
HDAC1
—
AR
(direct interaction, two hybrid)
Gaughan et al., J Biol Chem 2002*
-
IRef Biogrid Interaction:
HDAC1
—
AR
(physical association, affinity chromatography technology)
Gaughan et al., J Biol Chem 2002*
-
IRef Hprd Interaction:
Complex of 17 proteins
(in vivo)
Niki et al., Mol Cancer Res 2003*
-
IRef Hprd Interaction:
AR
—
HDAC1
(in vivo)
Gaughan et al., J Biol Chem 2002*
-
IRef Hprd Interaction:
AR
—
HDAC1
(in vitro)
Gaughan et al., J Biol Chem 2002*
-
IRef Intact Interaction:
Complex of EZH2-HDAC2-HDAC1-AR
(physical association, anti bait coimmunoprecipitation)
Chng et al., EMBO J 2012*
-
IRef Ophid Interaction:
AR
—
HDAC1
(aggregation, interologs mapping)
Brown et al., Bioinformatics 2005
-
IRef Ophid Interaction:
AR
—
HDAC1
(aggregation, confirmational text mining)
Gaughan et al., J Biol Chem 2002*
Text-mined interactions from Literome
Zhang et al., Nucleic Acids Res 2005
:
Functionally,
Sin3A enhanced the ability of Ebp1 to repress transcription of
androgen receptor (AR) and E2F1 regulated genes
Iacopino et al., Int J Oncol 2008
(Prostatic Neoplasms) :
The goal of this study was to assess the
effects of an
HDAC inhibitor, valproic acid ( VA ), on proliferation, androgen-sensitivity,
androgen receptor levels and E-cadherin ( E-cad ) expression in human prostate cancer cells
Fialova et al., Oncol Rep 2013
:
Effect of
histone deacetylase and DNA methyltransferase inhibitors on the expression of the
androgen receptor gene in androgen independent prostate cancer cell lines