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Human Chondrosarcoma Cells Acquire an Epithelial-Like Gene Expression Pattern via an Epigenetic Switch: Evidence for Mesenchymal-Epithelial Transition during Sarcomagenesis
Chondrocytes are mesenchymally derived cells that reportedly acquire some epithelial characteristics; however, whether this is a progression through a mesenchymal to epithelial transition (MET) during chondrosarcoma development is still a matter of investigation. We observed that chondrosarcoma cell...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3087947/ https://www.ncbi.nlm.nih.gov/pubmed/21559267 http://dx.doi.org/10.1155/2011/598218 |
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author | Fitzgerald, Matthew P. Gourronc, Francoise Teoh, Melissa L. T. Provenzano, Matthew J. Case, Adam J. Martin, James A. Domann, Frederick E. |
author_facet | Fitzgerald, Matthew P. Gourronc, Francoise Teoh, Melissa L. T. Provenzano, Matthew J. Case, Adam J. Martin, James A. Domann, Frederick E. |
author_sort | Fitzgerald, Matthew P. |
collection | PubMed |
description | Chondrocytes are mesenchymally derived cells that reportedly acquire some epithelial characteristics; however, whether this is a progression through a mesenchymal to epithelial transition (MET) during chondrosarcoma development is still a matter of investigation. We observed that chondrosarcoma cells acquired the expression of four epithelial markers, E-cadherin,desmocollin 3, maspin, and 14-3-3σ, all of which are governed epigenetically through cytosine methylation. Indeed, loss of cytosine methylation was tightly associated with acquired expression of both maspin and 14-3-3σ in chondrosarcomas. In contrast, chondrocyte cells were negative for maspin and 14-3-3σ and displayed nearly complete DNA methylation. Robust activation of these genes was also observed in chondrocyte cells following 5-aza-dC treatment. We also examined the transcription factor snail which has been reported to be an important mediator of epithelial to mesenchymal transitions (EMTs). In chondrosarcoma cells snail is downregulated suggesting a role for loss of snail expression in lineage maintenance. Taken together, these results document an epigenetic switch associated with an MET-like phenomenon that accompanies chondrosarcoma progression. |
format | Text |
id | pubmed-3087947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-30879472011-05-10 Human Chondrosarcoma Cells Acquire an Epithelial-Like Gene Expression Pattern via an Epigenetic Switch: Evidence for Mesenchymal-Epithelial Transition during Sarcomagenesis Fitzgerald, Matthew P. Gourronc, Francoise Teoh, Melissa L. T. Provenzano, Matthew J. Case, Adam J. Martin, James A. Domann, Frederick E. Sarcoma Research Article Chondrocytes are mesenchymally derived cells that reportedly acquire some epithelial characteristics; however, whether this is a progression through a mesenchymal to epithelial transition (MET) during chondrosarcoma development is still a matter of investigation. We observed that chondrosarcoma cells acquired the expression of four epithelial markers, E-cadherin,desmocollin 3, maspin, and 14-3-3σ, all of which are governed epigenetically through cytosine methylation. Indeed, loss of cytosine methylation was tightly associated with acquired expression of both maspin and 14-3-3σ in chondrosarcomas. In contrast, chondrocyte cells were negative for maspin and 14-3-3σ and displayed nearly complete DNA methylation. Robust activation of these genes was also observed in chondrocyte cells following 5-aza-dC treatment. We also examined the transcription factor snail which has been reported to be an important mediator of epithelial to mesenchymal transitions (EMTs). In chondrosarcoma cells snail is downregulated suggesting a role for loss of snail expression in lineage maintenance. Taken together, these results document an epigenetic switch associated with an MET-like phenomenon that accompanies chondrosarcoma progression. Hindawi Publishing Corporation 2011 2011-03-17 /pmc/articles/PMC3087947/ /pubmed/21559267 http://dx.doi.org/10.1155/2011/598218 Text en Copyright © 2011 Matthew P. Fitzgerald et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Fitzgerald, Matthew P. Gourronc, Francoise Teoh, Melissa L. T. Provenzano, Matthew J. Case, Adam J. Martin, James A. Domann, Frederick E. Human Chondrosarcoma Cells Acquire an Epithelial-Like Gene Expression Pattern via an Epigenetic Switch: Evidence for Mesenchymal-Epithelial Transition during Sarcomagenesis |
title | Human Chondrosarcoma Cells Acquire an Epithelial-Like Gene
Expression Pattern via an Epigenetic Switch: Evidence for
Mesenchymal-Epithelial Transition during Sarcomagenesis |
title_full | Human Chondrosarcoma Cells Acquire an Epithelial-Like Gene
Expression Pattern via an Epigenetic Switch: Evidence for
Mesenchymal-Epithelial Transition during Sarcomagenesis |
title_fullStr | Human Chondrosarcoma Cells Acquire an Epithelial-Like Gene
Expression Pattern via an Epigenetic Switch: Evidence for
Mesenchymal-Epithelial Transition during Sarcomagenesis |
title_full_unstemmed | Human Chondrosarcoma Cells Acquire an Epithelial-Like Gene
Expression Pattern via an Epigenetic Switch: Evidence for
Mesenchymal-Epithelial Transition during Sarcomagenesis |
title_short | Human Chondrosarcoma Cells Acquire an Epithelial-Like Gene
Expression Pattern via an Epigenetic Switch: Evidence for
Mesenchymal-Epithelial Transition during Sarcomagenesis |
title_sort | human chondrosarcoma cells acquire an epithelial-like gene
expression pattern via an epigenetic switch: evidence for
mesenchymal-epithelial transition during sarcomagenesis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3087947/ https://www.ncbi.nlm.nih.gov/pubmed/21559267 http://dx.doi.org/10.1155/2011/598218 |
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