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New insights into the role of ID proteins in breast cancer metastasis: a MET affair

The establishment of lethal metastases depends on the capacity of a small number of cancer cells to regenerate a tumor after entering a target organ. Stankic and colleagues have identified a role for the inhibitor of differentiation protein, ID1, as a critical regulator of breast cancer stem-like pr...

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Detalles Bibliográficos
Autores principales: Teo, Wee Siang, Nair, Radhika, Swarbrick, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053215/
https://www.ncbi.nlm.nih.gov/pubmed/25927844
http://dx.doi.org/10.1186/bcr3654
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author Teo, Wee Siang
Nair, Radhika
Swarbrick, Alexander
author_facet Teo, Wee Siang
Nair, Radhika
Swarbrick, Alexander
author_sort Teo, Wee Siang
collection PubMed
description The establishment of lethal metastases depends on the capacity of a small number of cancer cells to regenerate a tumor after entering a target organ. Stankic and colleagues have identified a role for the inhibitor of differentiation protein, ID1, as a critical regulator of breast cancer stem-like properties and metastatic colonization. Under the control of tumor growth factor-beta signaling, ID1 induces mesenchymal-epithelial transition at the metastatic site by antagonizing the activity of the basic helix-loop-helix transcription factor Twist1. This study sheds light on mechanisms that initiate metastatic outgrowth, and strengthens the concept that epithelial-mesenchymal plasticity is crucial at different stages of metastasis.
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spelling pubmed-40532152014-11-15 New insights into the role of ID proteins in breast cancer metastasis: a MET affair Teo, Wee Siang Nair, Radhika Swarbrick, Alexander Breast Cancer Res Viewpoint The establishment of lethal metastases depends on the capacity of a small number of cancer cells to regenerate a tumor after entering a target organ. Stankic and colleagues have identified a role for the inhibitor of differentiation protein, ID1, as a critical regulator of breast cancer stem-like properties and metastatic colonization. Under the control of tumor growth factor-beta signaling, ID1 induces mesenchymal-epithelial transition at the metastatic site by antagonizing the activity of the basic helix-loop-helix transcription factor Twist1. This study sheds light on mechanisms that initiate metastatic outgrowth, and strengthens the concept that epithelial-mesenchymal plasticity is crucial at different stages of metastasis. BioMed Central 2014 2014-05-15 /pmc/articles/PMC4053215/ /pubmed/25927844 http://dx.doi.org/10.1186/bcr3654 Text en Copyright © 2014 Teo et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 The licensee has exclusive rights to distribute this article, in any medium, for 6 months following its publication. After this time, the article is available under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Viewpoint
Teo, Wee Siang
Nair, Radhika
Swarbrick, Alexander
New insights into the role of ID proteins in breast cancer metastasis: a MET affair
title New insights into the role of ID proteins in breast cancer metastasis: a MET affair
title_full New insights into the role of ID proteins in breast cancer metastasis: a MET affair
title_fullStr New insights into the role of ID proteins in breast cancer metastasis: a MET affair
title_full_unstemmed New insights into the role of ID proteins in breast cancer metastasis: a MET affair
title_short New insights into the role of ID proteins in breast cancer metastasis: a MET affair
title_sort new insights into the role of id proteins in breast cancer metastasis: a met affair
topic Viewpoint
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053215/
https://www.ncbi.nlm.nih.gov/pubmed/25927844
http://dx.doi.org/10.1186/bcr3654
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