C/EBPalpha redirects androgen receptor signaling through a unique bimodal interaction.

Abstract

Nuclear expression of CCAAT enhancer binding protein-alpha (C/EBPalpha), which supports tissue differentiation through several antiproliferative protein-protein interactions, augurs terminal differentiation of prostate epithelial cells. C/EBPalpha is also a tumor suppressor, but in many tumors its antiproliferative interactions may be attenuated by de-phosphorylation. C/EBPalpha acts as a corepressor of the classical androgen response element (ARE)-mediated gene activation by the androgen receptor (AR), but this is paradoxical as the genotropic actions of AR are crucial not only for the growth of the prostate but also for its maintenance and function. We show that DNA-bound C/EPBalpha recruits AR to activate transcription. C/EBPalpha-dependent trans-activation by AR also overrode suppression of AREs by C/EBPalpha elsewhere in a promoter. This mechanism was remarkable in that its androgen dependence was apparently for nuclear translocation of AR; it was otherwise androgen independent, flutamide insensitive and tolerant to disruption of AR dimerization. Gene response profiles and global chromatin associations in situ supported the direct bimodal regulation of AR transcriptional signaling by C/EBPalpha. This unique mechanism explains the functional coordination between AR and C/EPBalpha in the prostate and also shows that hormone-refractory AR signaling in prostate cancer could occur through receptor tethering.

• Authors: J Zhang, M Gonit, M D Salazar, A Shatnawi, L Shemshedini, R Trumbly, M Ratnam
• Journal: Oncogene (Oncogene) Vol. 29 Issue 5 Pg. 723-38 (Feb 04 2010) ISSN: 1476-5594 [Electronic] England
• PMID: 19901962 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)

Chemical References

• CCAAT-Enhancer-Binding Protein-alpha
• RNA, Messenger
• RNA, Small Interfering
• Receptors, Androgen

Topics

• Blotting, Western
• CCAAT-Enhancer-Binding Protein-alpha (genetics, metabolism)
• Fluorescent Antibody Technique
• Gene Expression Regulation (physiology)
• HeLa Cells
• Humans
• Immunoprecipitation
• Male
• Microscopy, Confocal
• Oligonucleotide Array Sequence Analysis
• Prostatic Neoplasms (genetics, metabolism)
• RNA, Messenger (analysis)
• RNA, Small Interfering
• Receptors, Androgen (genetics, metabolism)
• Reverse Transcriptase Polymerase Chain Reaction
• Signal Transduction (physiology)
• Transcriptional Activation (physiology)
• Transfection