Document Detail


Regulation of the functional interaction between cyclin D1 and the estrogen receptor.
MedLine Citation:
PMID:  11073968     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We report that the functional interaction between cyclin D1 and the estrogen receptor (ER) is regulated by a signal transduction pathway involving the second messenger, cyclic AMP (cAMP). The cell-permeable cAMP analogue 8-bromo-cAMP caused a concentration-dependent enhancement of cyclin D1-ER complex formation, as judged both by coimmunoprecipitation and mammalian two-hybrid analysis. This effect was paralleled by increases in ligand-independent ER-mediated transcription from an estrogen response element containing reporter construct. These effects of 8-bromo-cAMP were antagonized by a specific protein kinase A (PKA) inhibitor, indicating that the signaling pathway involved was PKA dependent. Further, we show that culture of MCF-7 cells on a cellular substratum of murine preadipocytes also enhanced the functional interaction between cyclin D1 and ER in a PKA-dependent manner. These findings demonstrate a collaboration between cAMP signaling and cyclin D1 in the ligand-independent activation of ER-mediated transcription in mammary epithelial cells and show that the functional associations of cyclin D1 are regulated as a function of cellular context.
Authors:
J Lamb; M H Ladha; C McMahon; R L Sutherland; M E Ewen
Related Documents :
22266668 - Chronic glp-1 receptor activation by exendin-4 induces expansion of pancreatic duct gla...
12538508 - Erbb (her) receptors can abrogate antiestrogen action in human breast cancer by multipl...
11872838 - Imaging sites of receptor dephosphorylation by ptp1b on the surface of the endoplasmic ...
18519638 - Als-linked mutant sod1 induces er stress- and ask1-dependent motor neuron death by targ...
17418088 - Phosphoenolpyruvate metabolism in jerusalem artichoke mitochondria.
23493838 - Profile of bosutinib and its clinical potential in the treatment of chronic myeloid leu...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Molecular and cellular biology     Volume:  20     ISSN:  0270-7306     ISO Abbreviation:  Mol. Cell. Biol.     Publication Date:  2000 Dec 
Date Detail:
Created Date:  2000-12-19     Completed Date:  2000-12-19     Revised Date:  2013-04-17    
Medline Journal Info:
Nlm Unique ID:  8109087     Medline TA:  Mol Cell Biol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  8667-75     Citation Subset:  IM    
Affiliation:
Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts 02115, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
8-Bromo Cyclic Adenosine Monophosphate / pharmacology
Adipocytes / metabolism
Animals
Breast / metabolism
Breast Neoplasms / metabolism*
Cell Communication
Cells, Cultured
Coculture Techniques
Cyclin D1 / metabolism*
Epithelial Cells / metabolism
Estradiol / pharmacology
Humans
Ligands
Mice
Protein Binding / drug effects
Rats
Receptors, Estrogen / metabolism*
Stromal Cells / metabolism
Grant Support
ID/Acronym/Agency:
P01 CA80111/CA/NCI NIH HHS
Chemical
Reg. No./Substance:
0/Ligands; 0/Receptors, Estrogen; 136601-57-5/Cyclin D1; 23583-48-4/8-Bromo Cyclic Adenosine Monophosphate; 50-28-2/Estradiol
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Identification and characterization of an activating TrkA deletion mutation in acute myeloid leukemi...
Next Document:  Inhibitor of the tissue-specific transcription factor HNF4, a potential regulator in early Xenopus d...