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Epidermal growth factor binding and steroid receptor content in human benign prostatic hyperplasia
C Lubrano1, E Petrangeli, A Catizone
1Clinica Medica V, University of Rome, La Sapienza, Italy.
Journal of Steroid Biochemistry
|January 1, 1989
Summary
Epidermal growth factor receptors (EGF-R) were identified in benign prostatic hyperplasia (BPH) tissue. These receptors showed specific binding, and their levels correlated with steroid receptors, suggesting EGF
Area of Science:
- Endocrinology
- Molecular Biology
- Urology
Background:
- Benign prostatic hyperplasia (BPH) is a common condition in aging men.
- Epidermal growth factor receptor (EGF-R) plays a role in cell growth and proliferation.
- The role of EGF-R in BPH pathogenesis is not fully understood.
Purpose of the Study:
- To characterize the epidermal growth factor receptor (EGF-R) in human benign prostatic hyperplasia (BPH) tissue.
- To investigate the relationship between EGF-R and steroid receptors (estrogen, progesterone, androgen) in BPH.
Main Methods:
- Membrane fractions from human BPH tissue were used for EGF-R characterization.
- Radioligand binding assays with [125I]EGF were performed to determine binding kinetics and affinity.
- Steroid receptor levels were measured using the dextran-coated charcoal method.
Main Results:
- Specific binding sites for EGF-R were identified in BPH membranes with high and low affinities (Kd = 0.35 nM and 9.60 nM).
- Binding equilibrium was reached within 40 minutes at 25°C and remained stable.
- A significant negative correlation was observed between nuclear steroid receptor levels and EGF-R binding capacity.
Conclusions:
- Human BPH tissue possesses specific, high-affinity binding sites for EGF.
- The expression of EGF-R in BPH is modulated by steroid receptors.
- These findings suggest a potential role for EGF in the development or progression of prostatic hyperplasia.