mProX™ Human ESR2 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Nuclear Receptor
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Published Data
Fig.1 Regulation of SMR3A expression by ESR2 signaling.
Immunofluorescence labeling b (red signal) showed that fractionated IR promoted basal expression of ESR2 but not ESR1 protein in tumor cell lines, as revealed by Western blot analysis. Hoechst H33342 was used as a counterstain for cell nuclei (blue signal).
Ref: Grünow, Jennifer, et al. "Regulation of submaxillary gland androgen-regulated protein 3A via estrogen receptor 2 in radioresistant head and neck squamous cell carcinoma cells." Journal of Experimental & Clinical Cancer Research 36 (2017): 1-9.
Pubmed: 28166815
DOI: 10.1186/s13046-017-0496-2
Research Highlights
The transcription factor known as estrogen receptor alpha (ERα, encoded by ESR1) is extensively studied and shown to be expressed in over 75% of breast cancers. It is the primary biomarker used to guide endocrine therapy.
Dalal, Hina, et al. "Clinical associations of ESR2 (estrogen receptor beta) expression across thousands of primary breast tumors." Scientific Reports 12.1 (2022): 4696.
Pubmed:
35304506
DOI:
10.1038/s41598-022-08210-3
According to the findings, the absence of ESR2 increased the levels of granulosa and oocyte components, which can help activate mTOR and AKT in ovaries that are Esr2-/-, which in turn increases the activation of primordial follicles.
Chakravarthi, V. Praveen, et al. "A gatekeeping role of ESR2 to maintain the primordial follicle reserve." Endocrinology 161.4 (2020): bqaa037.
Pubmed:
32141511
DOI:
10.1210/endocr/bqaa037