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Epigenetic disruption of cadherin-11 in human cancer metastasis
Little is known about the molecular events occurring in the metastases of human tumours. Epigenetic alterations are dynamic lesions that change over the natural course of the disease, and so they might play a role in the biology of cancer cells that have departed from the primary tumour. Herein, we...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd.
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467766/ https://www.ncbi.nlm.nih.gov/pubmed/22374749 http://dx.doi.org/10.1002/path.4011 |
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author | Carmona, F Javier Villanueva, Alberto Vidal, August Muñoz, Clara Puertas, Sara Penin, Rosa M Gomà, Montserrat Lujambio, Amaia Piulats, Josep M Mesía, Ricard Sánchez-Céspedes, Montse Manós, Manel Condom, Enric Eccles, Suzanne A Esteller, Manel |
author_facet | Carmona, F Javier Villanueva, Alberto Vidal, August Muñoz, Clara Puertas, Sara Penin, Rosa M Gomà, Montserrat Lujambio, Amaia Piulats, Josep M Mesía, Ricard Sánchez-Céspedes, Montse Manós, Manel Condom, Enric Eccles, Suzanne A Esteller, Manel |
author_sort | Carmona, F Javier |
collection | PubMed |
description | Little is known about the molecular events occurring in the metastases of human tumours. Epigenetic alterations are dynamic lesions that change over the natural course of the disease, and so they might play a role in the biology of cancer cells that have departed from the primary tumour. Herein, we have adopted an epigenomic approach to identify some of these changes. Using a DNA methylation microarray platform to compare paired primary tumour and lymph node metastatic cell lines from the same patient, we observed cadherin-11 promoter CpG island hypermethylation as a likely target of the process. We found that CDH11 DNA methylation-associated transcriptional silencing occurred in the corresponding lymph node metastases of melanoma and head and neck cancer cells but not in the primary tumours. Using in vitro and in vivo cellular and mouse models for depleted or enhanced CDH11 activity, we also demonstrated that CDH11 acts as an inhibitor of tumour growth, motility and dissemination. Most importantly, the study of CDH11 5′-CpG island hypermethylation in primary tumours and lymph node metastases of cancer patients showed this epigenetic alteration to be significantly confined to the disseminated cells. Overall, these results indicate the existence of metastasis-specific epigenetic events that might contribute to the progression of the disease. Copyright © 2012 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd. |
format | Online Article Text |
id | pubmed-3467766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | John Wiley & Sons, Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-34677662012-10-12 Epigenetic disruption of cadherin-11 in human cancer metastasis Carmona, F Javier Villanueva, Alberto Vidal, August Muñoz, Clara Puertas, Sara Penin, Rosa M Gomà, Montserrat Lujambio, Amaia Piulats, Josep M Mesía, Ricard Sánchez-Céspedes, Montse Manós, Manel Condom, Enric Eccles, Suzanne A Esteller, Manel J Pathol Original Papers Little is known about the molecular events occurring in the metastases of human tumours. Epigenetic alterations are dynamic lesions that change over the natural course of the disease, and so they might play a role in the biology of cancer cells that have departed from the primary tumour. Herein, we have adopted an epigenomic approach to identify some of these changes. Using a DNA methylation microarray platform to compare paired primary tumour and lymph node metastatic cell lines from the same patient, we observed cadherin-11 promoter CpG island hypermethylation as a likely target of the process. We found that CDH11 DNA methylation-associated transcriptional silencing occurred in the corresponding lymph node metastases of melanoma and head and neck cancer cells but not in the primary tumours. Using in vitro and in vivo cellular and mouse models for depleted or enhanced CDH11 activity, we also demonstrated that CDH11 acts as an inhibitor of tumour growth, motility and dissemination. Most importantly, the study of CDH11 5′-CpG island hypermethylation in primary tumours and lymph node metastases of cancer patients showed this epigenetic alteration to be significantly confined to the disseminated cells. Overall, these results indicate the existence of metastasis-specific epigenetic events that might contribute to the progression of the disease. Copyright © 2012 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd. John Wiley & Sons, Ltd. 2012-10 2012-07-26 /pmc/articles/PMC3467766/ /pubmed/22374749 http://dx.doi.org/10.1002/path.4011 Text en Copyright © 2012 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd. 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 | Original Papers Carmona, F Javier Villanueva, Alberto Vidal, August Muñoz, Clara Puertas, Sara Penin, Rosa M Gomà, Montserrat Lujambio, Amaia Piulats, Josep M Mesía, Ricard Sánchez-Céspedes, Montse Manós, Manel Condom, Enric Eccles, Suzanne A Esteller, Manel Epigenetic disruption of cadherin-11 in human cancer metastasis |
title | Epigenetic disruption of cadherin-11 in human cancer metastasis |
title_full | Epigenetic disruption of cadherin-11 in human cancer metastasis |
title_fullStr | Epigenetic disruption of cadherin-11 in human cancer metastasis |
title_full_unstemmed | Epigenetic disruption of cadherin-11 in human cancer metastasis |
title_short | Epigenetic disruption of cadherin-11 in human cancer metastasis |
title_sort | epigenetic disruption of cadherin-11 in human cancer metastasis |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467766/ https://www.ncbi.nlm.nih.gov/pubmed/22374749 http://dx.doi.org/10.1002/path.4011 |
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