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Genistein inhibits the contact-stimulated migration of prostate cancer cells

The results of several epidemiological studies have suggested that a soybean-based diet is associated with a lower risk of prostate cancer. We investigated the effect of the soy isoflavone genistein on the proliferation and contact-stimulated migration of rat prostatic carcinoma MAT-LyLu and AT-2 ce...

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Detalles Bibliográficos
Autores principales: Miękus, Katarzyna, Madeja, Zbigniew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Versita 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275706/
https://www.ncbi.nlm.nih.gov/pubmed/17297558
http://dx.doi.org/10.2478/s11658-007-0007-0
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author Miękus, Katarzyna
Madeja, Zbigniew
author_facet Miękus, Katarzyna
Madeja, Zbigniew
author_sort Miękus, Katarzyna
collection PubMed
description The results of several epidemiological studies have suggested that a soybean-based diet is associated with a lower risk of prostate cancer. We investigated the effect of the soy isoflavone genistein on the proliferation and contact-stimulated migration of rat prostatic carcinoma MAT-LyLu and AT-2 cell lines. Genistein almost completely inhibited the growth of both MAT-LyLu and AT-2 cells in the concentration range from 25 to 100 μM, but the addition of 1 μM genistein to the medium significantly stimulated the proliferation of both cell lines. Additionally, at concentrations above 25 μM, genistein showed a potent cytotoxic effect. However, the central finding of this study is that at physiologically relevant concentrations (1 μM and 10 μM), genistein inhibits the motility of prostate cancer cells stimulated by homo-and heterotypic contacts. These results show that at physiological concentrations, genistein exerts an inhibitory effect on the migration of prostate cancer cells and suggest that it may be one of the factors responsible for the anti-metastatic activity of plant isoflavonoids
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spelling pubmed-62757062018-12-10 Genistein inhibits the contact-stimulated migration of prostate cancer cells Miękus, Katarzyna Madeja, Zbigniew Cell Mol Biol Lett Article The results of several epidemiological studies have suggested that a soybean-based diet is associated with a lower risk of prostate cancer. We investigated the effect of the soy isoflavone genistein on the proliferation and contact-stimulated migration of rat prostatic carcinoma MAT-LyLu and AT-2 cell lines. Genistein almost completely inhibited the growth of both MAT-LyLu and AT-2 cells in the concentration range from 25 to 100 μM, but the addition of 1 μM genistein to the medium significantly stimulated the proliferation of both cell lines. Additionally, at concentrations above 25 μM, genistein showed a potent cytotoxic effect. However, the central finding of this study is that at physiologically relevant concentrations (1 μM and 10 μM), genistein inhibits the motility of prostate cancer cells stimulated by homo-and heterotypic contacts. These results show that at physiological concentrations, genistein exerts an inhibitory effect on the migration of prostate cancer cells and suggest that it may be one of the factors responsible for the anti-metastatic activity of plant isoflavonoids Versita 2007-02-13 /pmc/articles/PMC6275706/ /pubmed/17297558 http://dx.doi.org/10.2478/s11658-007-0007-0 Text en © University of Wrocław 2007
spellingShingle Article
Miękus, Katarzyna
Madeja, Zbigniew
Genistein inhibits the contact-stimulated migration of prostate cancer cells
title Genistein inhibits the contact-stimulated migration of prostate cancer cells
title_full Genistein inhibits the contact-stimulated migration of prostate cancer cells
title_fullStr Genistein inhibits the contact-stimulated migration of prostate cancer cells
title_full_unstemmed Genistein inhibits the contact-stimulated migration of prostate cancer cells
title_short Genistein inhibits the contact-stimulated migration of prostate cancer cells
title_sort genistein inhibits the contact-stimulated migration of prostate cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275706/
https://www.ncbi.nlm.nih.gov/pubmed/17297558
http://dx.doi.org/10.2478/s11658-007-0007-0
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