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The insulin-like growth factor system in the prostate
D M Peehl1, P Cohen, R G Rosenfeld
1Department of Urology, Stanford University School of Medicine, CA 94305-5118, USA.
World Journal of Urology
|January 1, 1995
Summary
The insulin-like growth factor (IGF) system regulates prostate cell growth. Aberrations in this system are linked to benign prostatic hyperplasia (BPH), suggesting a role in prostate conditions.
Area of Science:
- Endocrinology
- Molecular Biology
- Urology
Background:
- The insulin-like growth factor (IGF) system comprises IGFs, receptors, binding proteins, and proteases.
- This system is crucial for regulating cell growth and development.
- Its role in prostate physiology and pathology is an area of active investigation.
Purpose of the Study:
- To characterize the IGF system's components and functions within the prostate.
- To investigate the expression and activity of IGFs, receptors, and IGF-binding proteins (IGFBPs) in prostatic cells.
- To explore the potential involvement of the IGF system in benign prostatic hyperplasia (BPH).
Main Methods:
- Analysis of IGF system components in prostatic cell lines and primary cultures (epithelial and stromal cells).
- Assessment of IGF receptor expression and signaling pathways.
- Examination of IGFBP synthesis, secretion, and proteolytic modification by prostate-specific antigen (PSA).
Main Results:
- Prostatic epithelial and stromal cells express IGF receptors and respond to IGF mitogenic activity.
- Prostatic stromal cells synthesize and secrete IGF-II; IGF synthesis in epithelial cells requires further confirmation.
- Multiple IGFBPs are secreted by prostatic cells, with IGFBP-3 cleavage by PSA demonstrated. Aberrations in the IGF system were noted in BPH-derived stromal cells.
Conclusions:
- The IGF system is present and active in the prostate, influencing cell growth via type I IGF receptors.
- The interaction between IGFBPs, PSA, and prostatic cells highlights complex regulatory mechanisms.
- Alterations in the IGF system are associated with BPH, suggesting its potential role in the etiology of this condition and other prostate diseases.