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ESR1 — HDAC1
Pathways - manually collected, often from reviews:
-
NCI Pathway Database Validated nuclear estrogen receptor alpha network:
LMO4 (LMO4)
→
ERA/MTA1/HDAC1/LMO4 complex (ESR1-MTA1-HDAC1-LMO4)
(modification, collaborate)
Mazumdar et al., Nat Cell Biol 2001, Singh et al., Cancer Res 2005
Evidence: mutant phenotype, physical interaction
-
NCI Pathway Database Validated nuclear estrogen receptor alpha network:
ER alpha (ESR1)
→
ERA/MTA1/HDAC1/LMO4 complex (ESR1-MTA1-HDAC1-LMO4)
(modification, collaborate)
Mazumdar et al., Nat Cell Biol 2001, Singh et al., Cancer Res 2005
Evidence: mutant phenotype, physical interaction
-
NCI Pathway Database Validated nuclear estrogen receptor alpha network:
ER alpha (ESR1)
→
HDAC1 (HDAC1)
(modification, collaborate)
Mazumdar et al., Nat Cell Biol 2001, Singh et al., Cancer Res 2005
Evidence: mutant phenotype, physical interaction
-
NCI Pathway Database Validated nuclear estrogen receptor alpha network:
ERA/MTA1/HDAC1/LMO4 complex (ESR1-MTA1-HDAC1-LMO4)
→
MTA1 (MTA1)
(modification, collaborate)
Mazumdar et al., Nat Cell Biol 2001, Singh et al., Cancer Res 2005
Evidence: mutant phenotype, physical interaction
-
NCI Pathway Database Validated nuclear estrogen receptor alpha network:
ERA/MTA1/HDAC1/LMO4 complex (ESR1-MTA1-HDAC1-LMO4)
→
HDAC1 (HDAC1)
(modification, collaborate)
Mazumdar et al., Nat Cell Biol 2001, Singh et al., Cancer Res 2005
Evidence: mutant phenotype, physical interaction
Protein-Protein interactions - manually collected from original source literature:
Studies that report less than 10 interactions are marked with *
-
IRef Bind_translation Interaction:
HDAC1
—
ESR1
(coimmunoprecipitation)
Kawai et al., Int J Cancer 2003*
-
IRef Bind_translation Interaction:
HDAC1
—
ESR1
(affinity chromatography technology)
Kawai et al., Int J Cancer 2003*
-
IRef Biogrid Interaction:
HDAC1
—
ESR1
(physical association, affinity chromatography technology)
Okada et al., EMBO Rep 2008
-
IRef Biogrid Interaction:
HDAC1
—
ESR1
(physical association, affinity chromatography technology)
Tarallo et al., Proteomics 2011
-
IRef Biogrid Interaction:
HDAC1
—
ESR1
(physical association, affinity chromatography technology)
Kawai et al., Int J Cancer 2003*
-
IRef Biogrid Interaction:
HDAC1
—
ESR1
(direct interaction, pull down)
Kawai et al., Int J Cancer 2003*
-
IRef Biogrid Interaction:
HDAC1
—
ESR1
(physical association, affinity chromatography technology)
Varshochi et al., J Biol Chem 2005*
-
IRef Biogrid Interaction:
HDAC1
—
ESR1
(physical association, affinity chromatography technology)
Kurtev et al., J Biol Chem 2004
-
IRef Biogrid Interaction:
HDAC1
—
ESR1
(colocalization, imaging technique)
Liu et al., J Biol Chem 2004*
-
IRef Biogrid Interaction:
HDAC1
—
ESR1
(physical association, affinity chromatography technology)
Itoh et al., J Immunol 2007*
-
IRef Intact Interaction:
Complex of CHD3-MTA1-HDAC1-ESR1
(association, anti bait coimmunoprecipitation)
Okada et al., EMBO Rep 2008
-
IRef Intact Interaction:
Complex of 13 proteins
(association, anti tag coimmunoprecipitation)
Okada et al., EMBO Rep 2008
Text-mined interactions from Literome
Macaluso et al., Oncogene 2003
(Breast Neoplasms) :
pRb2/p130-E2F4/5-HDAC1-SUV39H1-p300 and pRb2/p130-E2F4/5-HDAC1-SUV39H1-DNMT1 multimolecular complexes
mediate the transcription of
estrogen receptor-alpha in breast cancer
Kawai et al., Int J Cancer 2003
(Breast Neoplasms...) :
Interestingly, overexpression of
HDAC1 in stable transfected MCF-7 clones
induced loss of
ER-alpha and significantly increased cell proliferation and colony formation, as compared to the control MCF-7 cells, whereas treatment of stable MCF-7 clones with the HDAC specific inhibitor trichostatin A (TSA) induced re-expression of ER-alpha mRNA and protein
Keen et al., Breast Cancer Res Treat 2003
(Breast Neoplasms) :
A novel
histone deacetylase inhibitor, scriptaid,
enhances expression of functional
estrogen receptor alpha ( ER ) in ER negative human breast cancer cells in combination with 5-aza 2'-deoxycytidine
Margueron et al., J Mol Endocrinol 2004
(Breast Neoplasms) :
In this study, we have analysed the
effects of
histone deacetylase (HDAC) inhibition on
estrogen receptor ( ER ) expression and on its transcriptional activity in response to antiestrogens
Ellison-Zelski et al., Mol Cell Biol 2009
:
Reduction of
Sin3A expression by RNA interference specifically
inhibits estrogen induced repression of
ESR1
Khurana et al., J Biol Chem 2011
(Breast Neoplasms) :
In contrast,
histone deacetylase 7 (HDAC7)
inhibits estrogen receptor a ( ERa ) -mediated transcription