The objective of the present application is to employ the cell biology approach in an attempt to further understand the intimate structural and functional relationship among various cell types that characterize benign prostatic hyperplasia (BPH) development. The prostate consists of two basic components: STOMA and EPITHELIA. The latter can further be separated into the secretory cells and basal cells. Whether or not BPH development is associated with an altered cell-cell interaction remains to be an important question which will be addressed in this application. The use of various culture procedures permits us to examine the biological properties of individual cell types and combinations of them. Furthermore, by employing the newly developed techniques of two-dimensional gel electrophoresis and immunocytochemistry to characterize cytoskeletal proteins and prostate-associated specific proteins, we are able to assess the structural and organizational properties of various human prostatic cells in culture. The following specific aims are proposed: 1. Cultivation and characterization of epithelial and mesenchymal components from neonatal, normal, and hyperplastic human prostate. 2. Cultivation and characterization of epithelial and mesenchymal components from peripheral and periurethral zones of the human prostate. 3. Assessment of biological and biochemical properties of stromal and epithelial cells and their interactions under a variety of culture conditions. 4. Characterization of prostatic stromal and epithelial cells and their combination grown in nude mice and comparison of their biological properties with those grown in vitro.

Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Northwestern University at Chicago
Department
Type
DUNS #
005436803
City
Chicago
State
IL
Country
United States
Zip Code
60611
Ilio, K Y; Nemeth, J A; Sensibar, J A et al. (2000) Prostatic ductal system in rats: changes in regional distribution of extracellular matrix proteins during castration-induced regression. Prostate 43:10-Mar
Kassen, A E; Sensibar, J A; Sintich, S M et al. (2000) Autocrine effect of DHT on FGF signaling and cell proliferation in LNCaP cells: role of heparin/heparan-degrading enzymes. Prostate 44:124-32
Lee, C; Sintich, S M; Mathews, E P et al. (1999) Transforming growth factor-beta in benign and malignant prostate. Prostate 39:285-90
Sensibar, J A; Pruden, S J; Kasjanski, R Z et al. (1999) Differential growth rates in stromal cultures of human prostate derived from patients of varying ages. Prostate 38:110-7
Kim, I Y; Ahn, H J; Lang, S et al. (1998) Loss of expression of transforming growth factor-beta receptors is associated with poor prognosis in prostate cancer patients. Clin Cancer Res 4:1625-30
Kim, I Y; Zelner, D J; Lee, C (1998) The conventional transforming growth factor-beta (TGF-beta) receptor type I is not required for TGF-beta 1 signaling in a human prostate cancer cell line, LNCaP. Exp Cell Res 241:151-60
Grayhack, J T; Kozlowski, J M; Lee, C (1998) The pathogenesis of benign prostatic hyperplasia: a proposed hypothesis and critical evaluation. J Urol 160:2375-80
Sherwood, E R; Van Dongen, J L; Wood, C G et al. (1998) Epidermal growth factor receptor activation in androgen-independent but not androgen-stimulated growth of human prostatic carcinoma cells. Br J Cancer 77:855-61
Grayhack, J T; Sensibar, J A; Ilio, K Y et al. (1998) Synergistic action of steroids and spermatocele fluid on in vitro proliferation of prostate stroma. J Urol 159:2202-9
Gann, P H; Chatterton, R; Vogelsong, K et al. (1997) Epidermal growth factor-related peptides in human prostatic fluid: sources of variability in assay results. Prostate 32:234-40

Showing the most recent 10 out of 59 publications