Literature DB >> 7899150

Inhibition of prostatic epithelial cell proliferation by a factor secreted specifically by prostatic stromal cells.

A Kooistra1, J J König, D M Keizer, J C Romijn, F H Schröder.   

Abstract

Stromal cells from the prostate were recently shown to inhibit clonal growth of the prostatic carcinoma cell lines PC-3 (hormone-independent) and LNCaP (hormone-sensitive) in coculture. Our study revealed that stromal cell-conditioned medium strongly inhibited proliferation of PC-3 and LNCaP cells when grown in monolayer culture. Antiproliferative activity was found to be reversible, and was produced specifically by prostatic stromal cells and not by stromal cells derived from skin, foreskin, uterus, kidney, and Wilms' tumor. Inhibition was not species-specific, since the cell lines AT-2.1 and MATLyLu, derived from the Dunning rat prostate tumor, were also sensitive. No inhibition, however, occurred on breast and renal carcinoma cell lines, suggesting a prostate-specific action. The putative inhibiting factor(s) could be concentrated and partially purified by ammonium sulfate precipitation. The possible role in stromal control of epithelial cell proliferation is discussed.

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Year:  1995        PMID: 7899150     DOI: 10.1002/pros.2990260304

Source DB:  PubMed          Journal:  Prostate        ISSN: 0270-4137            Impact factor:   4.104


  3 in total

1.  Hepatocyte growth factor secreted by prostate-derived stromal cells stimulates growth of androgen-independent human prostatic carcinoma cells.

Authors:  K Nakashiro; M Okamoto; Y Hayashi; R Oyasu
Journal:  Am J Pathol       Date:  2000-09       Impact factor: 4.307

2.  EPN: a novel epithelial cell line derived from human prostate tissue.

Authors:  Antonio A Sinisi; Paolo Chieffi; Daniela Pasquali; Annamaria Kisslinger; Stefania Staibano; Antonio Bellastella; Donatella Tramontano
Journal:  In Vitro Cell Dev Biol Anim       Date:  2002-03       Impact factor: 2.416

3.  Stromal inhibition of prostatic epithelial cell proliferation not mediated by transforming growth factor beta.

Authors:  A Kooistra; A J van den Eijnden-van Raaij; I A Klaij; J C Romijn; F H Schröder
Journal:  Br J Cancer       Date:  1995-08       Impact factor: 7.640

  3 in total

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