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DNA methylation profiling reveals a predominant immune component in breast cancers
Breast cancer is a molecularly, biologically and clinically heterogeneous group of disorders. Understanding this diversity is essential to improving diagnosis and optimizing treatment. Both genetic and acquired epigenetic abnormalities participate in cancer, but the involvement of the epigenome in b...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3377115/ https://www.ncbi.nlm.nih.gov/pubmed/21910250 http://dx.doi.org/10.1002/emmm.201100801 |
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author | Dedeurwaerder, Sarah Desmedt, Christine Calonne, Emilie Singhal, Sandeep K Haibe-Kains, Benjamin Defrance, Matthieu Michiels, Stefan Volkmar, Michael Deplus, Rachel Luciani, Judith Lallemand, Françoise Larsimont, Denis Toussaint, Jérôme Haussy, Sandy Rothé, Françoise Rouas, Ghizlane Metzger, Otto Majjaj, Samira Saini, Kamal Putmans, Pascale Hames, Gérald van Baren, Nicolas Coulie, Pierre G Piccart, Martine Sotiriou, Christos Fuks, François |
author_facet | Dedeurwaerder, Sarah Desmedt, Christine Calonne, Emilie Singhal, Sandeep K Haibe-Kains, Benjamin Defrance, Matthieu Michiels, Stefan Volkmar, Michael Deplus, Rachel Luciani, Judith Lallemand, Françoise Larsimont, Denis Toussaint, Jérôme Haussy, Sandy Rothé, Françoise Rouas, Ghizlane Metzger, Otto Majjaj, Samira Saini, Kamal Putmans, Pascale Hames, Gérald van Baren, Nicolas Coulie, Pierre G Piccart, Martine Sotiriou, Christos Fuks, François |
author_sort | Dedeurwaerder, Sarah |
collection | PubMed |
description | Breast cancer is a molecularly, biologically and clinically heterogeneous group of disorders. Understanding this diversity is essential to improving diagnosis and optimizing treatment. Both genetic and acquired epigenetic abnormalities participate in cancer, but the involvement of the epigenome in breast cancer and its contribution to the complexity of the disease are still poorly understood. By means of DNA methylation profiling of 248 breast tissues, we have highlighted the existence of previously unrecognized breast cancer groups that go beyond the currently known ‘expression subtypes’. Interestingly, we showed that DNA methylation profiling can reflect the cell type composition of the tumour microenvironment, and in particular a T lymphocyte infiltration of the tumours. Further, we highlighted a set of immune genes having high prognostic value in specific tumour categories. The immune component uncovered here by DNA methylation profiles provides a new perspective for the importance of the microenvironment in breast cancer, holding implications for better management of breast cancer patients. |
format | Online Article Text |
id | pubmed-3377115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | WILEY-VCH Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-33771152012-09-17 DNA methylation profiling reveals a predominant immune component in breast cancers Dedeurwaerder, Sarah Desmedt, Christine Calonne, Emilie Singhal, Sandeep K Haibe-Kains, Benjamin Defrance, Matthieu Michiels, Stefan Volkmar, Michael Deplus, Rachel Luciani, Judith Lallemand, Françoise Larsimont, Denis Toussaint, Jérôme Haussy, Sandy Rothé, Françoise Rouas, Ghizlane Metzger, Otto Majjaj, Samira Saini, Kamal Putmans, Pascale Hames, Gérald van Baren, Nicolas Coulie, Pierre G Piccart, Martine Sotiriou, Christos Fuks, François EMBO Mol Med Research Article Breast cancer is a molecularly, biologically and clinically heterogeneous group of disorders. Understanding this diversity is essential to improving diagnosis and optimizing treatment. Both genetic and acquired epigenetic abnormalities participate in cancer, but the involvement of the epigenome in breast cancer and its contribution to the complexity of the disease are still poorly understood. By means of DNA methylation profiling of 248 breast tissues, we have highlighted the existence of previously unrecognized breast cancer groups that go beyond the currently known ‘expression subtypes’. Interestingly, we showed that DNA methylation profiling can reflect the cell type composition of the tumour microenvironment, and in particular a T lymphocyte infiltration of the tumours. Further, we highlighted a set of immune genes having high prognostic value in specific tumour categories. The immune component uncovered here by DNA methylation profiles provides a new perspective for the importance of the microenvironment in breast cancer, holding implications for better management of breast cancer patients. WILEY-VCH Verlag 2011-12 /pmc/articles/PMC3377115/ /pubmed/21910250 http://dx.doi.org/10.1002/emmm.201100801 Text en Copyright © 2011 EMBO Molecular Medicine |
spellingShingle | Research Article Dedeurwaerder, Sarah Desmedt, Christine Calonne, Emilie Singhal, Sandeep K Haibe-Kains, Benjamin Defrance, Matthieu Michiels, Stefan Volkmar, Michael Deplus, Rachel Luciani, Judith Lallemand, Françoise Larsimont, Denis Toussaint, Jérôme Haussy, Sandy Rothé, Françoise Rouas, Ghizlane Metzger, Otto Majjaj, Samira Saini, Kamal Putmans, Pascale Hames, Gérald van Baren, Nicolas Coulie, Pierre G Piccart, Martine Sotiriou, Christos Fuks, François DNA methylation profiling reveals a predominant immune component in breast cancers |
title | DNA methylation profiling reveals a predominant immune component in breast cancers |
title_full | DNA methylation profiling reveals a predominant immune component in breast cancers |
title_fullStr | DNA methylation profiling reveals a predominant immune component in breast cancers |
title_full_unstemmed | DNA methylation profiling reveals a predominant immune component in breast cancers |
title_short | DNA methylation profiling reveals a predominant immune component in breast cancers |
title_sort | dna methylation profiling reveals a predominant immune component in breast cancers |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3377115/ https://www.ncbi.nlm.nih.gov/pubmed/21910250 http://dx.doi.org/10.1002/emmm.201100801 |
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