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. 2023 Mar 9;11(3):826. doi: 10.3390/biomedicines11030826

Table 1.

Expression of ERα and ERβ in castration-resistant prostate cancer study model.

Study Model Estrogen Receptor Findings Author
Human PC-3 cell line ERβ ERβ regulates the cell cycle of PCa by controlling the expression of CCND1
(p < 0.05)
[63]
Tissue microarray consisting of PCa samples from CRPC patients (n = 101) ERα
ERβ
ERα ↓
ERβ1 ↑ (p < 0.05)
[57]
Human PC-3 cell line ERα ERα ↑ [37]
Human PC-3 and LNCaP cell lines ERβ1 ERβ1 and 3β-Adiol repress mesenchymal characteristics
VEGF-A and EMT expression ↓ (p < 0.05)
TGF-β and hypoxia reduced expression of ERβ1
[55]
Blood-derived RNA samples from CRPC patients (n = 42) ERα
ERβ
Detection of four mutations of ERα (E380Q, L536Q, Y537S and D538G)
ERβ splice variant concentrations ↓
[45]
Public genomic datasets from patients with metastatic or advanced prostate cancer (n= 150) and patients with early prostate cancer (n = 492) ERα
ERβ
The prevalence of ERα and ERβ mutations:
  • 3% in patients with metastatic or advanced PCa;

  • 2% with early stage of PCa

[85]
Primary tumor tissue from radical prostatectomy (RP) patients (n = 535) ERβ ERβ was correlated with decreased time to biochemical failure (BF) (p = 0.002) [46]
Human PC-3 (derived from bone metastasis) and DU-145 (derived from brain metastasis) cell lines ERα
ERβ
ERα activation via PPT (ERα-selective agonist)
ERβ activation via DPN (ERβ-selective agonist)
Both ERα and ERβ increase the migration and invasion of PC-3 cell lines
[35]

Abbreviations: ↑: increase; ↓: decrease; PPT: propylpyrazoletriol; DPN: diarylprepionitrile; CCND1: cyclin D1; EMT: epithelial-mesenchymal transition; VEGF-A: vascular endothelial growth factor A; biochemical failure: BF.