Ligand-dependent interaction between estrogen receptor alpha and adenomatous polyposis coli.

Abstract

Numerous independent clinical and experimental studies indicate that estrogens confer a protective effect against development of intestinal tumors, however the molecular mechanisms involved remain unclear. Physiological effects of estrogens are predominantly mediated by the action of nuclear estrogen receptors (ERs). A multifunctional protein adenomatous polyposis coli (APC) is a tumor suppressor and thought to act as a gatekeeper in colon tumorigenesis, as loss of function APC mutations trigger the development of colorectal cancer. Here we report that APC physically associates with ERa in the ligand-dependent manner. We have shown in the endogenous setting that the ligand-activated ERa recruits APC to the promoters in ER target genes and that increased levels of ER-dependent recruitment of APC enhances the ER transactivation through stimulation of histone acetylation. Found in majority of human colon tumors APC truncation mutants lost the ability to interact with ER. Thus, here we present the first evidence of a functional interaction between APC and ER that may be accounted for a tumor protective action of estrogens.

• Authors: Alexander P Kouzmenko, Ken-ichi Takeyama, Yoshihiro Kawasaki, Tetsu Akiyama, Shigeaki Kato
• Journal: Genes to cells : devoted to molecular & cellular mechanisms (Genes Cells) Vol. 13 Issue 7 Pg. 723-30 (Jul 2008) ISSN: 1365-2443 [Electronic] England
• PMID: 18498351 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Adenomatous Polyposis Coli Protein
• Estrogen Receptor alpha
• Estrogens
• Ligands

Topics

• Adenomatous Polyposis Coli (metabolism)
• Adenomatous Polyposis Coli Protein (genetics, metabolism)
• Amino Acid Sequence
• Estrogen Receptor alpha (metabolism)
• Estrogens (physiology)
• Genes, APC
• HCT116 Cells
• Humans
• Ligands
• Response Elements (physiology)
• Sequence Deletion
• Transcriptional Activation (physiology)