2012
DOI: 10.1016/j.steroids.2012.02.011
|View full text |Cite
|
Sign up to set email alerts
|

Early membrane initiated transcriptional effects of estrogens in breast cancer cells: First pharmacological evidence for a novel membrane estrogen receptor element (ERx)

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
5

Citation Types

0
30
0

Year Published

2013
2013
2022
2022

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 28 publications
(30 citation statements)
references
References 53 publications
0
30
0
Order By: Relevance
“…A different receptor, functionally distinct form of ERα and ERβ, was identified by Almey et al [49] and was named ER-X. ER-X can be illustrious from previously labeled receptors inter alia by its molecular weight which is 63 kDa, while the molecular weight of ERα, ERβ, and Gpr30 was 67 kDa, 60 kDa, and 44 kDa, respectively [50]. Additionally, it does not involve in the stimulation of extracellular signal-controlled kinases in the presence of selective estrogen receptor agonists and responds more powerfully to 17α than 17β estradiol [45].…”
Section: Membrane Receptors Specific To Estrogensmentioning
confidence: 99%
See 2 more Smart Citations
“…A different receptor, functionally distinct form of ERα and ERβ, was identified by Almey et al [49] and was named ER-X. ER-X can be illustrious from previously labeled receptors inter alia by its molecular weight which is 63 kDa, while the molecular weight of ERα, ERβ, and Gpr30 was 67 kDa, 60 kDa, and 44 kDa, respectively [50]. Additionally, it does not involve in the stimulation of extracellular signal-controlled kinases in the presence of selective estrogen receptor agonists and responds more powerfully to 17α than 17β estradiol [45].…”
Section: Membrane Receptors Specific To Estrogensmentioning
confidence: 99%
“…Additionally, it does not involve in the stimulation of extracellular signal-controlled kinases in the presence of selective estrogen receptor agonists and responds more powerfully to 17α than 17β estradiol [45]. ere was an another discovery of receptor in T47D and MCF-7 cells by Kampa et al [50] which are related to cell signaling, apoptosis, and transcriptional regulation [51]. e receptor was surprisingly named ERx even though there is no proof that ER-X and Erx are associated.…”
Section: Membrane Receptors Specific To Estrogensmentioning
confidence: 99%
See 1 more Smart Citation
“…It is relevant to mention that except for the well-known classical ERs and GPER, several novel membrane-associated receptors such as ER-X [48], ER-x [49] and STX-binding protein [50] have been proposed as oestrogen receptors. Since the definition of ERs is missing, it remains a matter of debate whether these later described receptors are really oestrogen receptors [51], and their further characterization is required.…”
Section: Oestrogen Receptorsmentioning
confidence: 99%
“…ER-X has a sequence homology to ERα, binds estradiol with high affinity, activates extracellular signal-regulated kinases ERK1/2, is developmentally regulated in the neocortex and uterus with maximal expression at postnatal days 7–10, and may be re-expressed in the adult brain after injury [48]. ER-x was described as a membrane ER that mediates oestrogen signalling in some breast cancer cell lines, leading to the modulation of apoptosis, growth factor signalling and transcriptional regulation [49]. Whether these receptors also play a role in male reproduction remains to be determined.…”
Section: Oestrogen Receptorsmentioning
confidence: 99%