Ligand-independent activation of steroid hormone receptors
- PMID: 9660165
- DOI: 10.1007/s001090050241
Ligand-independent activation of steroid hormone receptors
Abstract
In addition to the conventional hormone-dependent regulation of the activity of steroid/thyroid receptor family members, many studies have shown that there is substantial cross-talk between signal transduction pathways and steroid receptors. In a number of cases the modulation of kinase/phosphatase activity in cells leads to activation of steroid receptors in the absence of hormone. This novel mechanism may not be ubiquitous as the glucocorticoid receptor appears to be refractory to activation in the absence of hormone. However, estrogen receptors, progesterone receptors, androgen receptors, retinoic acid receptors, retinoid X receptors, and vitamin D receptors all exhibit ligand-independent activation under appropriate conditions. Whether a steroid receptor responds to a signal by inducing transcription of a target gene in the absence of hormone depends upon the cell type, promoter, and activator. The mechanism(s) by which ligand-independent activation is induced is currently a subject of great interest. Because the signals that activate receptors induce protein phosphorylation, altered phosphorylation of the receptors, and/or proteins that associate with the receptors are likely to be key to ligand-independent activation. In the case of the estrogen receptor there is good evidence that altered receptor phosphorylation plays a role in ligand-independent activation. Other likely targets are proteins in the heat shock protein complexes, corepressors, and/or coactivators of steroid receptors.
Comment in
-
Steroid hormone action 1998: novel challenges for drug design.J Mol Med (Berl). 1998 Jun;76(7):459-60. doi: 10.1007/s001090050238. J Mol Med (Berl). 1998. PMID: 9660162 No abstract available.
Similar articles
-
The role of coactivators and corepressors in the biology and mechanism of action of steroid hormone receptors.J Mammary Gland Biol Neoplasia. 2000 Jul;5(3):307-24. doi: 10.1023/a:1009503029176. J Mammary Gland Biol Neoplasia. 2000. PMID: 14973393 Review.
-
Steroid hormone receptors and their regulation by phosphorylation.Biochem J. 1996 Nov 1;319 ( Pt 3)(Pt 3):657-67. doi: 10.1042/bj3190657. Biochem J. 1996. PMID: 8920964 Free PMC article. Review.
-
Role of co-activators and co-repressors in the mechanism of steroid/thyroid receptor action.Recent Prog Horm Res. 1997;52:141-64; discussion 164-5. Recent Prog Horm Res. 1997. PMID: 9238851 Review.
-
Fatty acids: ancestral ligands and modern co-regulators of the steroid hormone receptor cell signalling pathway.Prostaglandins Leukot Essent Fatty Acids. 1995 Feb-Mar;52(2-3):137-44. doi: 10.1016/0952-3278(95)90012-8. Prostaglandins Leukot Essent Fatty Acids. 1995. PMID: 7784449 Review.
-
Ligand-dependent cross-talk between steroid and thyroid hormone receptors. Evidence for common transcriptional coactivator(s).J Biol Chem. 1996 Jun 21;271(25):14825-33. J Biol Chem. 1996. PMID: 8662980
Cited by
-
Collagen-IV and laminin-1 regulate estrogen receptor alpha expression and function in mouse mammary epithelial cells.J Cell Sci. 2003 Jul 15;116(Pt 14):2975-86. doi: 10.1242/jcs.00523. J Cell Sci. 2003. PMID: 12808020 Free PMC article.
-
The Nuclear Receptor Field: A Historical Overview and Future Challenges.Nucl Receptor Res. 2018;5:101320. doi: 10.11131/2018/101320. Epub 2018 Jul 26. Nucl Receptor Res. 2018. PMID: 30148160 Free PMC article.
-
Androgen Receptor Structure, Function and Biology: From Bench to Bedside.Clin Biochem Rev. 2016 Feb;37(1):3-15. Clin Biochem Rev. 2016. PMID: 27057074 Free PMC article. Review.
-
Ligand-independent activation of androgen receptors by Rho GTPase signaling in prostate cancer.Mol Endocrinol. 2008 Mar;22(3):597-608. doi: 10.1210/me.2007-0158. Epub 2007 Dec 13. Mol Endocrinol. 2008. PMID: 18079321 Free PMC article.
-
Endocrine Resistance in Hormone Receptor Positive Breast Cancer-From Mechanism to Therapy.Front Endocrinol (Lausanne). 2019 May 24;10:245. doi: 10.3389/fendo.2019.00245. eCollection 2019. Front Endocrinol (Lausanne). 2019. PMID: 31178825 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources