Estrogen receptor beta
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Estrogen receptor beta (ER-β), also known as NR3A2 (nuclear receptor subfamily 3, group A, member 2), is one of two main types of estrogen receptor, a nuclear receptor which is activated by the sex hormone estrogen.[1] In humans, ER-β is encoded by the ESR2 gene.[2]
Contents
Function
ER-β is a member of the family of estrogen receptors and the superfamily of nuclear receptor transcription factors. The gene product contains an N-terminal DNA binding domain and C-terminal ligand binding domain and is localized to the nucleus, cytoplasm, and mitochondria. Upon binding to 17-β-estradiol, estriol or related ligands, the encoded protein forms homo-dimers or hetero-dimers with estrogen receptor α that interact with specific DNA sequences to activate transcription. Some isoforms dominantly inhibit the activity of other estrogen receptor family members. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been fully characterized.[3]
ER-β may have anti-proliferative effects and therefore oppose the actions of ERα in reproductive tissue.[4] ER-β may also have an important role in adaptive function of the lung during pregnancy.[5]
ER-β is a potent tumor suppressor and plays a crucial role in many cancer types such as prostate cancer.[6]
Tissue distribution
ER-β is expressed by many tissues including the uterus,[7] blood monocytes and tissue macrophages, colonic and pulmonary epithelial cells and in prostatic epithelium and in malignant counterparts of these tissues. Also, ER-β is found throughout the brain at different concentrations in different neuron clusters.[8][9]
ER-β abnormalities
ER-β function is related to various cardiovascular targets including ATP-binding cassette transporter A1 (ABCA1) and apolipoprotein A1 (ApoA-1). Polymorphism may affect ER-β function and lead to altered responses in postmenopausal women receiving hormone replacement therapy.[10]
Ligands
Agonists
Agonists of ER-β selective over ERα include:
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- 3β-Androstanediol (3β-diol) – endogenous
- 8β-VE2
- AC-186
- Apigenin – phytoestrogen[11]
- Daidzein – phytoestrogen[11]
- Dehydroepiandrosterone (DHEA) – endogenous
- Diarylpropionitrile (DPN)
- ERB-196 (WAY-202196)
- FERb 033 – 62-fold selectivity for ER-β over ERα[12]
- Genistein – phytoestrogen; 16-fold selectivity for ER-β over ERα[11]
- Kaempferol – phytoestrogen[11]
- Liquiritigenin (Menerba) – phytoestrogen[11]
- Penduletin – phytoestrogen[11]
- Prinaberel (ERB-041, WAY-202041)
- S-Equol ((S)-4',7-isoflavandiol) – phytoestrogen; 13-fold selectivity for ER-β over ERα[11]
- WAY-166818
- WAY-200070
Antagonists
Antagonists of ER-β selective over ERα include:
- PHTPP
- (R,R)-Tetrahydrochrysene ((R,R)-THC) – not actually selective over ERα, but rather an agonist instead of antagonist of ERα
Interactions
Estrogen receptor beta has been shown to interact with:
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References
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Further reading
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External links
- Estrogen Receptor beta at the US National Library of Medicine Medical Subject Headings (MeSH)
This article incorporates text from the United States National Library of Medicine, which is in the public domain.