Skrzypczak, M. and Kapka-Skrzypczak, L. and Cyranka, M. and Treeck, O. and Wrobel, A. and Matosiuk, D. (2013) Nuclear Estrogen Receptors Co-activation Mechanisms. CURRENT MEDICINAL CHEMISTRY, 20 (27). pp. 3317-3338. ISSN 0929-8673, 1875-533X
Full text not available from this repository. (Request a copy)Abstract
Estrogens play very important role in opening the transcription event, which is a final step of activation of the first order mediators as receptors or channels in the cell wall by information coming from the outside of the cell. For the long time the exact step by step mechanism of cellular transfer of information to the cell nuclei was not known. Currently many new informations are available. Very important seems the step of phosphorylation and therefore desensitization of the target proteins. All peptide kinases, especially serine and threonine, like protein kinases A and C, RAS and MAP kinases, cycline kinases are potential or confirmed biological targets. Except them elements of the transcription complexes like p160.SRC-1, histon acetyltransferase and histon deacetylase, CBP/p300, TRAP/DRIP, NSD1, PPAR gamma/PGC-1, NCOR1, SMRT, REA were also found useful. Finally estrogens are able to activate other receptors, namely aryl hydrocarbon receptors (AhR) and estrogen receptor related proteins (ERR). It is well known that many types of cancer are related to the direct or indirect excessive activation of nuclear estrogen receptors, therefore their inhibition could be crucial in many estrogen-related cancers. Understanding the interactions in such complexes would help in developing new and better multi-target cures and finding new ligands with better pharmacological and pharmacokinetic properties.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | BREAST-CANCER-CELLS; ARYL-HYDROCARBON RECEPTOR; CYCLIN-DEPENDENT KINASE; LIGAND-INDEPENDENT ACTIVATION; STEROID-HORMONE RECEPTORS; BETA MESSENGER-RNA; ACTIVITY IN-VITRO; ALPHA ER-ALPHA; HISTONE DEACETYLASE INHIBITORS; DNA-BINDING DOMAIN; Estrogene receptors; estrogen co-activators; estrogen co-repressors; MAPK; histone acetyltransferase; histone deacetylase; aromatic hydrocarbon receptor; estrogen receptor related proteins; protein kinases; cyclase kinases; kinase inhibitors |
| Subjects: | 600 Technology > 610 Medical sciences Medicine |
| Divisions: | Medicine > Lehrstuhl für Frauenheilkunde und Geburtshilfe (Schwerpunkt Frauenheilkunde) |
| Depositing User: | Dr. Gernot Deinzer |
| Date Deposited: | 02 Apr 2020 13:13 |
| Last Modified: | 02 Apr 2020 13:13 |
| URI: | https://pred.uni-regensburg.de/id/eprint/16208 |
Actions (login required)
 |
View Item |
