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The epithelial–mesenchymal transition: new insights in signaling, development, and disease
The conversion of an epithelial cell to a mesenchymal cell is critical to metazoan embryogenesis and a defining structural feature of organ development. Current interest in this process, which is described as an epithelial–mesenchymal transition (EMT), stems from its developmental importance and its...
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2063755/ https://www.ncbi.nlm.nih.gov/pubmed/16567498 http://dx.doi.org/10.1083/jcb.200601018 |
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author | Lee, Jonathan M. Dedhar, Shoukat Kalluri, Raghu Thompson, Erik W. |
author_facet | Lee, Jonathan M. Dedhar, Shoukat Kalluri, Raghu Thompson, Erik W. |
author_sort | Lee, Jonathan M. |
collection | PubMed |
description | The conversion of an epithelial cell to a mesenchymal cell is critical to metazoan embryogenesis and a defining structural feature of organ development. Current interest in this process, which is described as an epithelial–mesenchymal transition (EMT), stems from its developmental importance and its involvement in several adult pathologies. Interest and research in EMT are currently at a high level, as seen by the attendance at the recent EMT meeting in Vancouver, Canada (October 1–3, 2005). The meeting, which was hosted by The EMT International Association, was the second international EMT meeting, the first being held in Port Douglas, Queensland, Australia in October 2003. The EMT International Association was formed in 2002 to provide an international body for those interested in EMT and the reverse process, mesenchymal–epithelial transition, and, most importantly, to bring together those working on EMT in development, cancer, fibrosis, and pathology. These themes continued during the recent meeting in Vancouver. Discussion at the Vancouver meeting spanned several areas of research, including signaling pathway activation of EMT and the transcription factors and gene targets involved. Also covered in detail was the basic cell biology of EMT and its role in cancer and fibrosis, as well as the identification of new markers to facilitate the observation of EMT in vivo. This is particularly important because the potential contribution of EMT during neoplasia is the subject of vigorous scientific debate (Tarin, D., E.W. Thompson, and D.F. Newgreen. 2005. Cancer Res. 65:5996–6000; Thompson, E.W., D.F. Newgreen, and D. Tarin. 2005. Cancer Res. 65:5991–5995). |
format | Text |
id | pubmed-2063755 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-20637552007-11-29 The epithelial–mesenchymal transition: new insights in signaling, development, and disease Lee, Jonathan M. Dedhar, Shoukat Kalluri, Raghu Thompson, Erik W. J Cell Biol Reviews The conversion of an epithelial cell to a mesenchymal cell is critical to metazoan embryogenesis and a defining structural feature of organ development. Current interest in this process, which is described as an epithelial–mesenchymal transition (EMT), stems from its developmental importance and its involvement in several adult pathologies. Interest and research in EMT are currently at a high level, as seen by the attendance at the recent EMT meeting in Vancouver, Canada (October 1–3, 2005). The meeting, which was hosted by The EMT International Association, was the second international EMT meeting, the first being held in Port Douglas, Queensland, Australia in October 2003. The EMT International Association was formed in 2002 to provide an international body for those interested in EMT and the reverse process, mesenchymal–epithelial transition, and, most importantly, to bring together those working on EMT in development, cancer, fibrosis, and pathology. These themes continued during the recent meeting in Vancouver. Discussion at the Vancouver meeting spanned several areas of research, including signaling pathway activation of EMT and the transcription factors and gene targets involved. Also covered in detail was the basic cell biology of EMT and its role in cancer and fibrosis, as well as the identification of new markers to facilitate the observation of EMT in vivo. This is particularly important because the potential contribution of EMT during neoplasia is the subject of vigorous scientific debate (Tarin, D., E.W. Thompson, and D.F. Newgreen. 2005. Cancer Res. 65:5996–6000; Thompson, E.W., D.F. Newgreen, and D. Tarin. 2005. Cancer Res. 65:5991–5995). The Rockefeller University Press 2006-03-27 /pmc/articles/PMC2063755/ /pubmed/16567498 http://dx.doi.org/10.1083/jcb.200601018 Text en Copyright © 2006, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Reviews Lee, Jonathan M. Dedhar, Shoukat Kalluri, Raghu Thompson, Erik W. The epithelial–mesenchymal transition: new insights in signaling, development, and disease |
title | The epithelial–mesenchymal transition: new insights in signaling, development, and disease |
title_full | The epithelial–mesenchymal transition: new insights in signaling, development, and disease |
title_fullStr | The epithelial–mesenchymal transition: new insights in signaling, development, and disease |
title_full_unstemmed | The epithelial–mesenchymal transition: new insights in signaling, development, and disease |
title_short | The epithelial–mesenchymal transition: new insights in signaling, development, and disease |
title_sort | epithelial–mesenchymal transition: new insights in signaling, development, and disease |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2063755/ https://www.ncbi.nlm.nih.gov/pubmed/16567498 http://dx.doi.org/10.1083/jcb.200601018 |
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