Literature DB >> 10519415

Carcinoma-associated fibroblasts direct tumor progression of initiated human prostatic epithelium.

A F Olumi1, G D Grossfeld, S W Hayward, P R Carroll, T D Tlsty, G R Cunha.   

Abstract

The present study demonstrates that fibroblasts associated with carcinomas stimulate tumor progression of initiated nontumorigenic epithelial cells both in an in vivo tissue recombination system and in an in vitro coculture system. Human prostatic carcinoma-associated fibroblasts grown with initiated human prostatic epithelial cells dramatically stimulated growth and altered histology of the epithelial population. This effect was not detected when normal prostatic fibroblasts were grown with the initiated epithelial cells under the same experimental conditions. In contrast, carcinoma-associated fibroblasts did not affect growth of normal human prostatic epithelial cells under identical conditions. From these data, we conclude that in this human prostate cancer model, carcinoma-associated fibroblasts stimulate progression of tumorigenesis. Thus, carcinoma-associated fibroblasts can direct tumor progression of an initiated prostate epithelial cell.

Entities:  

Keywords:  Non-programmatic

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Year:  1999        PMID: 10519415      PMCID: PMC3300837          DOI: 10.1186/bcr138

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


Full text

We have demonstrated that fibroblasts associated with carcinomas stimulate tumor progression of initiated non-tumorigenic epithelial cells both in an in vivo tissue recombination system and in an in vitro co-culture system. Human carcinoma-associated fibroblasts grown with initiated human epithelial cells dramatically stimulate growth and alter histology of epithelial cells. This effect is not detected when normal fibroblasts are grown with the same epithelial cells under the same experimental conditions. From these data and other data we conclude that, in this human cancer model, carcinoma-associated fibroblasts stimulate tumor progression of an initiated epithelial cell.
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