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Brachyury regulates proliferation of cancer cells via a p27(Kip1-)dependent pathway
The T-box transcription factor Brachyury is expressed in a number of tumour types and has been demonstrated to have cancer inducing properties. To date, it has been linked to cancer associated induction of epithelial to mesenchymal transition, tumour metastasis and expression of markers for cancer s...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4116522/ https://www.ncbi.nlm.nih.gov/pubmed/25003467 |
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author | Jezkova, Jana Williams, Jason S. Jones-Hutchins, Ffion Sammut, Stephen J. Gollins, Simon Cree, Ian Coupland, Sarah McFarlane, Ramsay J. Wakeman, Jane A. |
author_facet | Jezkova, Jana Williams, Jason S. Jones-Hutchins, Ffion Sammut, Stephen J. Gollins, Simon Cree, Ian Coupland, Sarah McFarlane, Ramsay J. Wakeman, Jane A. |
author_sort | Jezkova, Jana |
collection | PubMed |
description | The T-box transcription factor Brachyury is expressed in a number of tumour types and has been demonstrated to have cancer inducing properties. To date, it has been linked to cancer associated induction of epithelial to mesenchymal transition, tumour metastasis and expression of markers for cancer stem-like cells. Taken together, these findings indicate that Brachyury plays an important role in the progression of cancer, although the mechanism through which it functions is poorly understood. Here we show that Brachyury regulates the potential of Brachyury-positive colorectal cancer cells to proliferate and reduced levels of Brachyury result in inhibition of proliferation, with features consistent with the cells entering a quiescent-like state. This inhibition of proliferation is dependent upon p27(Kip1) demonstrating that Brachyury acts to modulate cellular proliferative fate in colorectal cancer cells in a p27(Kip1)-dependent manner. Analysis of patient derived colorectal tumours reveals a heterogeneous localisation of Brachyury (in the nucleolus, nucleus and cytoplasm) indicating the potential complexity of the regulatory role of Brachyury in solid colorectal tumours. |
format | Online Article Text |
id | pubmed-4116522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-41165222014-08-04 Brachyury regulates proliferation of cancer cells via a p27(Kip1-)dependent pathway Jezkova, Jana Williams, Jason S. Jones-Hutchins, Ffion Sammut, Stephen J. Gollins, Simon Cree, Ian Coupland, Sarah McFarlane, Ramsay J. Wakeman, Jane A. Oncotarget Research Paper The T-box transcription factor Brachyury is expressed in a number of tumour types and has been demonstrated to have cancer inducing properties. To date, it has been linked to cancer associated induction of epithelial to mesenchymal transition, tumour metastasis and expression of markers for cancer stem-like cells. Taken together, these findings indicate that Brachyury plays an important role in the progression of cancer, although the mechanism through which it functions is poorly understood. Here we show that Brachyury regulates the potential of Brachyury-positive colorectal cancer cells to proliferate and reduced levels of Brachyury result in inhibition of proliferation, with features consistent with the cells entering a quiescent-like state. This inhibition of proliferation is dependent upon p27(Kip1) demonstrating that Brachyury acts to modulate cellular proliferative fate in colorectal cancer cells in a p27(Kip1)-dependent manner. Analysis of patient derived colorectal tumours reveals a heterogeneous localisation of Brachyury (in the nucleolus, nucleus and cytoplasm) indicating the potential complexity of the regulatory role of Brachyury in solid colorectal tumours. Impact Journals LLC 2014-05-21 /pmc/articles/PMC4116522/ /pubmed/25003467 Text en Copyright: © 2014 Jezkova et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Jezkova, Jana Williams, Jason S. Jones-Hutchins, Ffion Sammut, Stephen J. Gollins, Simon Cree, Ian Coupland, Sarah McFarlane, Ramsay J. Wakeman, Jane A. Brachyury regulates proliferation of cancer cells via a p27(Kip1-)dependent pathway |
title | Brachyury regulates proliferation of cancer cells via a p27(Kip1-)dependent pathway |
title_full | Brachyury regulates proliferation of cancer cells via a p27(Kip1-)dependent pathway |
title_fullStr | Brachyury regulates proliferation of cancer cells via a p27(Kip1-)dependent pathway |
title_full_unstemmed | Brachyury regulates proliferation of cancer cells via a p27(Kip1-)dependent pathway |
title_short | Brachyury regulates proliferation of cancer cells via a p27(Kip1-)dependent pathway |
title_sort | brachyury regulates proliferation of cancer cells via a p27(kip1-)dependent pathway |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4116522/ https://www.ncbi.nlm.nih.gov/pubmed/25003467 |
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