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Reactive astrocytes promote the metastatic growth of breast cancer stem-like cells by activating Notch signalling in brain
Brain metastasis of breast cancer profoundly affects the cognitive and sensory functions as well as morbidity of patients, and the 1 year survival rate among these patients remains less than 20%. However, the pathological mechanism of brain metastasis is as yet poorly understood. In this report, we...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598079/ https://www.ncbi.nlm.nih.gov/pubmed/23495140 http://dx.doi.org/10.1002/emmm.201201623 |
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author | Xing, Fei Kobayashi, Aya Okuda, Hiroshi Watabe, Misako Pai, Sudha K Pandey, Puspa R Hirota, Shigeru Wilber, Andrew Mo, Yin-Yuan Moore, Brian E Liu, Wen Fukuda, Koji Iiizumi, Megumi Sharma, Sambad Liu, Yin Wu, Kerui Peralta, Elizabeth Watabe, Kounosuke |
author_facet | Xing, Fei Kobayashi, Aya Okuda, Hiroshi Watabe, Misako Pai, Sudha K Pandey, Puspa R Hirota, Shigeru Wilber, Andrew Mo, Yin-Yuan Moore, Brian E Liu, Wen Fukuda, Koji Iiizumi, Megumi Sharma, Sambad Liu, Yin Wu, Kerui Peralta, Elizabeth Watabe, Kounosuke |
author_sort | Xing, Fei |
collection | PubMed |
description | Brain metastasis of breast cancer profoundly affects the cognitive and sensory functions as well as morbidity of patients, and the 1 year survival rate among these patients remains less than 20%. However, the pathological mechanism of brain metastasis is as yet poorly understood. In this report, we found that metastatic breast tumour cells in the brain highly expressed IL-1β which then ‘activated’ surrounding astrocytes. This activation significantly augmented the expression of JAG1 in the astrocytes, and the direct interaction of the reactivated astrocytes and cancer stem-like cells (CSCs) significantly stimulated Notch signalling in CSCs. We also found that the activated Notch signalling in CSCs up-regulated HES5 followed by promoting self-renewal of CSCs. Furthermore, we have shown that the blood-brain barrier permeable Notch inhibitor, Compound E, can significantly suppress the brain metastasis in vivo. These results represent a novel paradigm for the understanding of how metastatic breast CSCs re-establish their niche for their self-renewal in a totally different microenvironment, which opens a new avenue to identify a novel and specific target for the brain metastatic disease. |
format | Online Article Text |
id | pubmed-3598079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | WILEY-VCH Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-35980792013-03-19 Reactive astrocytes promote the metastatic growth of breast cancer stem-like cells by activating Notch signalling in brain Xing, Fei Kobayashi, Aya Okuda, Hiroshi Watabe, Misako Pai, Sudha K Pandey, Puspa R Hirota, Shigeru Wilber, Andrew Mo, Yin-Yuan Moore, Brian E Liu, Wen Fukuda, Koji Iiizumi, Megumi Sharma, Sambad Liu, Yin Wu, Kerui Peralta, Elizabeth Watabe, Kounosuke EMBO Mol Med Research Articles Brain metastasis of breast cancer profoundly affects the cognitive and sensory functions as well as morbidity of patients, and the 1 year survival rate among these patients remains less than 20%. However, the pathological mechanism of brain metastasis is as yet poorly understood. In this report, we found that metastatic breast tumour cells in the brain highly expressed IL-1β which then ‘activated’ surrounding astrocytes. This activation significantly augmented the expression of JAG1 in the astrocytes, and the direct interaction of the reactivated astrocytes and cancer stem-like cells (CSCs) significantly stimulated Notch signalling in CSCs. We also found that the activated Notch signalling in CSCs up-regulated HES5 followed by promoting self-renewal of CSCs. Furthermore, we have shown that the blood-brain barrier permeable Notch inhibitor, Compound E, can significantly suppress the brain metastasis in vivo. These results represent a novel paradigm for the understanding of how metastatic breast CSCs re-establish their niche for their self-renewal in a totally different microenvironment, which opens a new avenue to identify a novel and specific target for the brain metastatic disease. WILEY-VCH Verlag 2013-03 2013-03-05 /pmc/articles/PMC3598079/ /pubmed/23495140 http://dx.doi.org/10.1002/emmm.201201623 Text en Copyright © 2013 The Authors. Published by John Wiley and Sons, Ltd on behalf of EMBO http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Research Articles Xing, Fei Kobayashi, Aya Okuda, Hiroshi Watabe, Misako Pai, Sudha K Pandey, Puspa R Hirota, Shigeru Wilber, Andrew Mo, Yin-Yuan Moore, Brian E Liu, Wen Fukuda, Koji Iiizumi, Megumi Sharma, Sambad Liu, Yin Wu, Kerui Peralta, Elizabeth Watabe, Kounosuke Reactive astrocytes promote the metastatic growth of breast cancer stem-like cells by activating Notch signalling in brain |
title | Reactive astrocytes promote the metastatic growth of breast cancer stem-like cells by activating Notch signalling in brain |
title_full | Reactive astrocytes promote the metastatic growth of breast cancer stem-like cells by activating Notch signalling in brain |
title_fullStr | Reactive astrocytes promote the metastatic growth of breast cancer stem-like cells by activating Notch signalling in brain |
title_full_unstemmed | Reactive astrocytes promote the metastatic growth of breast cancer stem-like cells by activating Notch signalling in brain |
title_short | Reactive astrocytes promote the metastatic growth of breast cancer stem-like cells by activating Notch signalling in brain |
title_sort | reactive astrocytes promote the metastatic growth of breast cancer stem-like cells by activating notch signalling in brain |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598079/ https://www.ncbi.nlm.nih.gov/pubmed/23495140 http://dx.doi.org/10.1002/emmm.201201623 |
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