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Differences between human breast cell lines in susceptibility towards growth inhibition by genistein

Genistein is thought to contribute to the putative breast cancer preventive activity of soya. The mechanisms by which it arrests the growth of breast cells are incompletely understood. In order to explore generic features of the modulation of human breast cell growth by genistein, its effects on cel...

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Autores principales: Dampier, K, Hudson, E A, Howells, L M, Manson, M M, Walker, R A, Gescher, A
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364092/
https://www.ncbi.nlm.nih.gov/pubmed/11506505
http://dx.doi.org/10.1054/bjoc.2001.1980
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author Dampier, K
Hudson, E A
Howells, L M
Manson, M M
Walker, R A
Gescher, A
author_facet Dampier, K
Hudson, E A
Howells, L M
Manson, M M
Walker, R A
Gescher, A
author_sort Dampier, K
collection PubMed
description Genistein is thought to contribute to the putative breast cancer preventive activity of soya. The mechanisms by which it arrests the growth of breast cells are incompletely understood. In order to explore generic features of the modulation of human breast cell growth by genistein, its effects on cell lines MCF-7, ZR-75.1, T47-D, MDA-MB 468, MDA-MB 231 and HBL 100 were compared. Genistein at 1 μM stimulated growth only in MCF-7 cells. At 10 μM it arrested the growth of all 6 cell types, however that of T47-D and HBL 100 cells only in medium with reduced (2%) fetal calf serum. Genistein induced apoptosis in only MDA-MB 468 cells. It arrested cells in the G2 stage of the cell cycle in all cell lines except ZR-75.1. Cells differed in their susceptibility towards inhibition by genistein of phorbol ester-induced proto-oncogene c-fos levels, transcription factor activator protein-1 (AP-1) activity and extracellular signal-regulated kinase (ERK) activity. Genistein augmented anisomycin-induced levels of proto-oncogene c-jun in ZR 75.1 and MCF-7 cells. The results suggest that induction of apoptosis, G2 cell cycle arrest and inhibition of c-fos expression, AP-1 transactivation and ERK phosphorylation may contribute to the growth-inhibitory effect of genistein in some breast cell types, but none of these effects of genistein constitutes a generic mode of growth-arresting action. © 2001 Cancer Research Campaign http://www.bjcancer.com
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spelling pubmed-23640922009-09-10 Differences between human breast cell lines in susceptibility towards growth inhibition by genistein Dampier, K Hudson, E A Howells, L M Manson, M M Walker, R A Gescher, A Br J Cancer Regular Article Genistein is thought to contribute to the putative breast cancer preventive activity of soya. The mechanisms by which it arrests the growth of breast cells are incompletely understood. In order to explore generic features of the modulation of human breast cell growth by genistein, its effects on cell lines MCF-7, ZR-75.1, T47-D, MDA-MB 468, MDA-MB 231 and HBL 100 were compared. Genistein at 1 μM stimulated growth only in MCF-7 cells. At 10 μM it arrested the growth of all 6 cell types, however that of T47-D and HBL 100 cells only in medium with reduced (2%) fetal calf serum. Genistein induced apoptosis in only MDA-MB 468 cells. It arrested cells in the G2 stage of the cell cycle in all cell lines except ZR-75.1. Cells differed in their susceptibility towards inhibition by genistein of phorbol ester-induced proto-oncogene c-fos levels, transcription factor activator protein-1 (AP-1) activity and extracellular signal-regulated kinase (ERK) activity. Genistein augmented anisomycin-induced levels of proto-oncogene c-jun in ZR 75.1 and MCF-7 cells. The results suggest that induction of apoptosis, G2 cell cycle arrest and inhibition of c-fos expression, AP-1 transactivation and ERK phosphorylation may contribute to the growth-inhibitory effect of genistein in some breast cell types, but none of these effects of genistein constitutes a generic mode of growth-arresting action. © 2001 Cancer Research Campaign http://www.bjcancer.com Nature Publishing Group 2001-08 /pmc/articles/PMC2364092/ /pubmed/11506505 http://dx.doi.org/10.1054/bjoc.2001.1980 Text en Copyright © 2001 Cancer Research Campaign https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Regular Article
Dampier, K
Hudson, E A
Howells, L M
Manson, M M
Walker, R A
Gescher, A
Differences between human breast cell lines in susceptibility towards growth inhibition by genistein
title Differences between human breast cell lines in susceptibility towards growth inhibition by genistein
title_full Differences between human breast cell lines in susceptibility towards growth inhibition by genistein
title_fullStr Differences between human breast cell lines in susceptibility towards growth inhibition by genistein
title_full_unstemmed Differences between human breast cell lines in susceptibility towards growth inhibition by genistein
title_short Differences between human breast cell lines in susceptibility towards growth inhibition by genistein
title_sort differences between human breast cell lines in susceptibility towards growth inhibition by genistein
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364092/
https://www.ncbi.nlm.nih.gov/pubmed/11506505
http://dx.doi.org/10.1054/bjoc.2001.1980
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