Nuclear receptor coregulators and human disease
- PMID: 17609497
- DOI: 10.1210/er.2007-0012
Nuclear receptor coregulators and human disease
Abstract
Nuclear receptor (NR) coregulators (coactivators and corepressors) are essential elements in regulating nuclear receptor-mediated transcription. In a little more than a decade since their discovery, these proteins have been studied mechanistically and reveal that the regulation of transcription is a highly controlled and complex process. Because of their central role in regulating NR-mediated transcription and in coordinating intercompartmental metabolic processes, disruptions in coregulator biology can lead to pathological states. To date, the extent to which they are involved in human disease has not been widely appreciated. In a complete literature survey, we have identified nearly 300 distinct coregulators, revealing that a great variety of enzymatic and regulatory capabilities exist for NRs to regulate transcription and other cellular events. Here, we substantiate that coregulators are broadly implicated in human pathological states and will be of growing future interest in clinical medicine.
Similar articles
-
Nuclear receptor coregulators: judges, juries, and executioners of cellular regulation.Mol Cell. 2007 Sep 7;27(5):691-700. doi: 10.1016/j.molcel.2007.08.012. Mol Cell. 2007. PMID: 17803935 Review.
-
Nuclear receptor coregulators: cellular and molecular biology.Endocr Rev. 1999 Jun;20(3):321-44. doi: 10.1210/edrv.20.3.0366. Endocr Rev. 1999. PMID: 10368774 Review.
-
Pharmacology of nuclear receptor-coregulator recognition.Vitam Horm. 2004;68:145-83. doi: 10.1016/S0083-6729(04)68005-8. Vitam Horm. 2004. PMID: 15193454 Review.
-
The Year in Basic Science: nuclear receptors and coregulators.Mol Endocrinol. 2008 Dec;22(12):2751-8. doi: 10.1210/me.2008-0297. Epub 2008 Oct 9. Mol Endocrinol. 2008. PMID: 18845672 Free PMC article. Review.
-
Corepressors of agonist-bound nuclear receptors.Toxicol Appl Pharmacol. 2007 Sep 15;223(3):288-98. doi: 10.1016/j.taap.2007.05.019. Epub 2007 Jun 14. Toxicol Appl Pharmacol. 2007. PMID: 17628626 Free PMC article. Review.
Cited by
-
Our evolving understanding of how 27-hydroxycholesterol influences cancer.Biochem Pharmacol. 2022 Feb;196:114621. doi: 10.1016/j.bcp.2021.114621. Epub 2021 May 24. Biochem Pharmacol. 2022. PMID: 34043965 Free PMC article. Review.
-
Drugging the unfolded protein response in acute leukemias.J Hematol Oncol. 2015 Jul 16;8:87. doi: 10.1186/s13045-015-0184-7. J Hematol Oncol. 2015. PMID: 26179601 Free PMC article. Review.
-
Steroid receptor coactivator (SRC) family: masters of systems biology.J Biol Chem. 2010 Dec 10;285(50):38743-50. doi: 10.1074/jbc.R110.193367. Epub 2010 Oct 18. J Biol Chem. 2010. PMID: 20956538 Free PMC article. Review.
-
Progesterone action in human tissues: regulation by progesterone receptor (PR) isoform expression, nuclear positioning and coregulator expression.Nucl Recept Signal. 2009 Dec 31;7:e009. doi: 10.1621/nrs.07009. Nucl Recept Signal. 2009. PMID: 20087430 Free PMC article. Review.
-
Circadian rhythm transcription factor CLOCK regulates the transcriptional activity of the glucocorticoid receptor by acetylating its hinge region lysine cluster: potential physiological implications.FASEB J. 2009 May;23(5):1572-83. doi: 10.1096/fj.08-117697. Epub 2009 Jan 13. FASEB J. 2009. PMID: 19141540 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical