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Genistein decreases the breast cancer stem-like cell population through Hedgehog pathway

INTRODUCTION: The existence of breast cancer stem-like cells (BCSCs) has profound implications for cancer prevention. Genistein, a predominant isoflavone found in soy products, has multiple robust anti-tumor effects in various cancers, especially in the breast and prostate cancer. In this study, we...

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Autores principales: Fan, Panhong, Fan, Shujun, Wang, Huan, Mao, Jun, Shi, Yu, Ibrahim, Mohammed M, Ma, Wei, Yu, Xiaotang, Hou, Zhenhuan, Wang, Bo, Li, Lianhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4054948/
https://www.ncbi.nlm.nih.gov/pubmed/24331293
http://dx.doi.org/10.1186/scrt357
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author Fan, Panhong
Fan, Shujun
Wang, Huan
Mao, Jun
Shi, Yu
Ibrahim, Mohammed M
Ma, Wei
Yu, Xiaotang
Hou, Zhenhuan
Wang, Bo
Li, Lianhong
author_facet Fan, Panhong
Fan, Shujun
Wang, Huan
Mao, Jun
Shi, Yu
Ibrahim, Mohammed M
Ma, Wei
Yu, Xiaotang
Hou, Zhenhuan
Wang, Bo
Li, Lianhong
author_sort Fan, Panhong
collection PubMed
description INTRODUCTION: The existence of breast cancer stem-like cells (BCSCs) has profound implications for cancer prevention. Genistein, a predominant isoflavone found in soy products, has multiple robust anti-tumor effects in various cancers, especially in the breast and prostate cancer. In this study, we aimed to evaluate genistein inhibition of BCSCs and its potential mechanism by culturing MCF-7 breast cancer cells and implanting these cells into nude mice. METHODS: Cell counting, colony formation and cell apoptosis analysis were used to evaluate the effect of genistein on breast cancer cells’ growth, proliferation and apoptosis. We then used mammosphere formation assay and CD44CD24 staining to evaluate the effect of genistein on BCSCs in vitro. A nude mice xenograft model was employed to determine whether genistein could target BCSCs in vivo, as assessed by real-time polymerase chain reaction (PCR) and immunohistochemical staining. The potential mechanism was investigated utilizing real-time PCR, western blotting analysis and immunohistochemical staining. RESULTS: Genistein inhibited the MCF-7 breast cancer cells’ growth and proliferation and promoted apoptosis. Both in vitro and in vivo genistein decreased breast cancer stem cells, and inhibited breast cancer stem-like cells through down-regulation of the Hedgehog-Gli1 Signaling Pathway. CONCLUSIONS: We demonstrated for the first time that genistein inhibits BCSCs by down-regulating Hedgehog-Gli1 signaling pathway. These findings provide support and rationale for investigating the clinical application of genistein in treating breast cancer, and specifically by targeting breast cancer stem cells.
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spelling pubmed-40549482014-06-20 Genistein decreases the breast cancer stem-like cell population through Hedgehog pathway Fan, Panhong Fan, Shujun Wang, Huan Mao, Jun Shi, Yu Ibrahim, Mohammed M Ma, Wei Yu, Xiaotang Hou, Zhenhuan Wang, Bo Li, Lianhong Stem Cell Res Ther Research INTRODUCTION: The existence of breast cancer stem-like cells (BCSCs) has profound implications for cancer prevention. Genistein, a predominant isoflavone found in soy products, has multiple robust anti-tumor effects in various cancers, especially in the breast and prostate cancer. In this study, we aimed to evaluate genistein inhibition of BCSCs and its potential mechanism by culturing MCF-7 breast cancer cells and implanting these cells into nude mice. METHODS: Cell counting, colony formation and cell apoptosis analysis were used to evaluate the effect of genistein on breast cancer cells’ growth, proliferation and apoptosis. We then used mammosphere formation assay and CD44CD24 staining to evaluate the effect of genistein on BCSCs in vitro. A nude mice xenograft model was employed to determine whether genistein could target BCSCs in vivo, as assessed by real-time polymerase chain reaction (PCR) and immunohistochemical staining. The potential mechanism was investigated utilizing real-time PCR, western blotting analysis and immunohistochemical staining. RESULTS: Genistein inhibited the MCF-7 breast cancer cells’ growth and proliferation and promoted apoptosis. Both in vitro and in vivo genistein decreased breast cancer stem cells, and inhibited breast cancer stem-like cells through down-regulation of the Hedgehog-Gli1 Signaling Pathway. CONCLUSIONS: We demonstrated for the first time that genistein inhibits BCSCs by down-regulating Hedgehog-Gli1 signaling pathway. These findings provide support and rationale for investigating the clinical application of genistein in treating breast cancer, and specifically by targeting breast cancer stem cells. BioMed Central 2013-12-11 /pmc/articles/PMC4054948/ /pubmed/24331293 http://dx.doi.org/10.1186/scrt357 Text en Copyright © 2013 Fan et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Fan, Panhong
Fan, Shujun
Wang, Huan
Mao, Jun
Shi, Yu
Ibrahim, Mohammed M
Ma, Wei
Yu, Xiaotang
Hou, Zhenhuan
Wang, Bo
Li, Lianhong
Genistein decreases the breast cancer stem-like cell population through Hedgehog pathway
title Genistein decreases the breast cancer stem-like cell population through Hedgehog pathway
title_full Genistein decreases the breast cancer stem-like cell population through Hedgehog pathway
title_fullStr Genistein decreases the breast cancer stem-like cell population through Hedgehog pathway
title_full_unstemmed Genistein decreases the breast cancer stem-like cell population through Hedgehog pathway
title_short Genistein decreases the breast cancer stem-like cell population through Hedgehog pathway
title_sort genistein decreases the breast cancer stem-like cell population through hedgehog pathway
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4054948/
https://www.ncbi.nlm.nih.gov/pubmed/24331293
http://dx.doi.org/10.1186/scrt357
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