Platelet-derived growth factor induces proliferation of hyperplastic human prostatic stromal cells

✍ Scribed by Dr. Chris J. Vlahos; Tracey D. Kriauciunas; Philip E. Gleason; Jeffrey A. Jones; John N. Eble; Dan Salvas; Julie F. Falcone; Kenneth S. Hirsch

• Publisher: John Wiley and Sons
• Year: 1993
• Tongue: English
• Weight: 990 KB
• Volume: 52
• Category: Article
• ISSN: 0730-2312
• DOI: 10.1002/jcb.240520405

✦ Synopsis

Abstract

Prostatic hyperplasia (BPH) is a very common disease in elderly men and is characterized by abnormal proliferation of the stromal and epithelial cells of the prostate. The observation that BPH often occurs in association with chronic inflammation has led to the examination of the possibility that platelet‐derived growth factor (PDGF), which is released in response to inflammation, may be an etiological factor in the genesis of the disease. It has been shown that cultured cells derived from human prostatic tissue express high affinity PDGF‐β receptors based on receptor binding and cross‐linking studies with [^125^I]‐PDGF‐BB. The experiments presented below demonstrate that PDGF receptors are activated in response to the growth factor and that mitogenesis is induced. PDGF‐BB treatment of cultured human prostate cells derived from patients with BPH activates the signal transduction pathway of the PDGF receptor as shown by the presence of several phosphoproteins in antiphosphotyrosine immunoprecipitates, including autophosphorylation of the PDGF receptor. Phosphatidylinositol (PI) 3‐kinase activity is also increased in cells stimulated with PDGF. The addition of PDGF‐BB to the medium causes a variable but dose‐dependent increase in [^3^H]‐thymidine incorporation. This paper describes the first demonstration that PDGF is a potent mitogen for human cells derived from patients exhibiting prostatic hyperplasia, and also demonstrates that the cellular response to PDGF‐BB is heterogeneous in a manner that is consistent with the varying degree of hyperplasia and inflammation clinically and histologically in the tissue specimens.