Korean J Urol.  1999 Nov;40(11):1478-1486.

Derivation of Androgen-Independent LNCaP Sublines from Cell-Cell Interactions of LNCaP and Human Prostate Fibroblasts in vivo

Affiliations
  • 1Department of urology, Catholic University College of Medicine, Seoul, Korea.
  • 2Department of urology, University of Virginia, Virginia, USA.

Abstract

PURPOSE: A cell-cell interaction in which in vivo inoculation of androgen-dependent, non-tumorigenic LNCaP and human bone fibroblast resulted in derivation of androgen-independent and metastatic LNCaP subline(C4-2) in castrated hosts. The purpose of this study is to evaluate if human prostate fibroblasts when grown together with LNCaP may promote androgen-independent growth and enhance metastatic potential.
MATERIALS AND METHODS
LNCaP cells and human prostate fibroblasts derived either from peripheral or transition zone co-inoculated in athymic mice for 8 weeks, and then mice were castrated. The chimeric tumors were maintained for additional 4 weeks. The LNCaP sublines, designated P4 and T4, were established and characterized. These sublines were co-inoculated again in castrated mice with human prostate fibroblasts for 8-12 weeks. And then second generation LNCaP sublines, P4-2 and T4-2, were established and also characterized.
RESULTS
Marked cytogenetic alterations were observed in P4-2, P4, T4-2 and T4 LNCaP sublines in comparison to parental LNCaP. Although LNCaP cells injected orthotopically did not form tumors in castrated hosts, LNCaP sublines formed PSA-producing tumors and had metastatic potentials to lymph node, lung, liver and bone. These P and T sublines had androgen-independent growth characteristics and metastatic potential.
CONCLUSIONS
Cell-cell interactions between prostatic epithelium and their surrounding fibroblasts could contribute to androgen-independent characteristics and enhanced metastatic potential of localized prostate cancer in vivo.

Keyword

Cell-cell interaction; LNCaP; Prostate fibroblast; Androgen-independent

MeSH Terms

Animals
Cytogenetics
Epithelium
Fibroblasts*
Humans*
Liver
Lung
Lymph Nodes
Mice
Mice, Nude
Parents
Prostate*
Prostatic Neoplasms
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