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Increased macroH2A1.1 Expression Correlates with Poor Survival of Triple-Negative Breast Cancer Patients
PURPOSE: Epithelial-Mesenchymal Transition (EMT) features appear to be key events in development and progression of breast cancer. Epigenetic modifications contribute to the establishment and maintenance of cancer subclasses, as well as to the EMT process. Whether histone variants contribute to thes...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049614/ https://www.ncbi.nlm.nih.gov/pubmed/24911873 http://dx.doi.org/10.1371/journal.pone.0098930 |
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author | Lavigne, Anne-Claire Castells, Magali Mermet, Jérôme Kocanova, Silvia Dalvai, Mathieu Bystricky, Kerstin |
author_facet | Lavigne, Anne-Claire Castells, Magali Mermet, Jérôme Kocanova, Silvia Dalvai, Mathieu Bystricky, Kerstin |
author_sort | Lavigne, Anne-Claire |
collection | PubMed |
description | PURPOSE: Epithelial-Mesenchymal Transition (EMT) features appear to be key events in development and progression of breast cancer. Epigenetic modifications contribute to the establishment and maintenance of cancer subclasses, as well as to the EMT process. Whether histone variants contribute to these transformations is not known. We investigated the relative expression levels of histone macroH2A1 splice variants and correlated it with breast cancer status/prognosis/types. METHODS: To detect differential expression of macroH2A1 variant mRNAs in breast cancer cells and tumor samples, we used the following databases: GEO, EMBL-EBI and publisher databases (may-august 2012). We extracted macroH2A1.1/macroH2A1 mRNA ratios and performed correlation studies on intrinsic molecular subclasses of breast cancer and on molecular characteristics of EMT. Associations between molecular and survival data were determined. RESULTS: We found increased macroH2A1.1/macroH2A1 mRNA ratios to be associated with the claudin-low intrinsic subtype in breast cancer cell lines. At the molecular level this association translates into a positive correlation between macroH2A1 ratios and molecular characteristics of the EMT process. Moreover, untreated Triple Negative Breast Cancers presenting a high macroH2A1.1 mRNA ratio exhibit a poor outcome. CONCLUSION: These results provide first evidence that macroH2A1.1 could be exploited as an actor in the maintenance of a transient cellular state in EMT progress towards metastatic development of breast tumors. |
format | Online Article Text |
id | pubmed-4049614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-40496142014-06-18 Increased macroH2A1.1 Expression Correlates with Poor Survival of Triple-Negative Breast Cancer Patients Lavigne, Anne-Claire Castells, Magali Mermet, Jérôme Kocanova, Silvia Dalvai, Mathieu Bystricky, Kerstin PLoS One Research Article PURPOSE: Epithelial-Mesenchymal Transition (EMT) features appear to be key events in development and progression of breast cancer. Epigenetic modifications contribute to the establishment and maintenance of cancer subclasses, as well as to the EMT process. Whether histone variants contribute to these transformations is not known. We investigated the relative expression levels of histone macroH2A1 splice variants and correlated it with breast cancer status/prognosis/types. METHODS: To detect differential expression of macroH2A1 variant mRNAs in breast cancer cells and tumor samples, we used the following databases: GEO, EMBL-EBI and publisher databases (may-august 2012). We extracted macroH2A1.1/macroH2A1 mRNA ratios and performed correlation studies on intrinsic molecular subclasses of breast cancer and on molecular characteristics of EMT. Associations between molecular and survival data were determined. RESULTS: We found increased macroH2A1.1/macroH2A1 mRNA ratios to be associated with the claudin-low intrinsic subtype in breast cancer cell lines. At the molecular level this association translates into a positive correlation between macroH2A1 ratios and molecular characteristics of the EMT process. Moreover, untreated Triple Negative Breast Cancers presenting a high macroH2A1.1 mRNA ratio exhibit a poor outcome. CONCLUSION: These results provide first evidence that macroH2A1.1 could be exploited as an actor in the maintenance of a transient cellular state in EMT progress towards metastatic development of breast tumors. Public Library of Science 2014-06-09 /pmc/articles/PMC4049614/ /pubmed/24911873 http://dx.doi.org/10.1371/journal.pone.0098930 Text en © 2014 Lavigne et al http://creativecommons.org/licenses/by/4.0/ 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 properly credited. |
spellingShingle | Research Article Lavigne, Anne-Claire Castells, Magali Mermet, Jérôme Kocanova, Silvia Dalvai, Mathieu Bystricky, Kerstin Increased macroH2A1.1 Expression Correlates with Poor Survival of Triple-Negative Breast Cancer Patients |
title | Increased macroH2A1.1 Expression Correlates with Poor Survival of Triple-Negative Breast Cancer Patients |
title_full | Increased macroH2A1.1 Expression Correlates with Poor Survival of Triple-Negative Breast Cancer Patients |
title_fullStr | Increased macroH2A1.1 Expression Correlates with Poor Survival of Triple-Negative Breast Cancer Patients |
title_full_unstemmed | Increased macroH2A1.1 Expression Correlates with Poor Survival of Triple-Negative Breast Cancer Patients |
title_short | Increased macroH2A1.1 Expression Correlates with Poor Survival of Triple-Negative Breast Cancer Patients |
title_sort | increased macroh2a1.1 expression correlates with poor survival of triple-negative breast cancer patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049614/ https://www.ncbi.nlm.nih.gov/pubmed/24911873 http://dx.doi.org/10.1371/journal.pone.0098930 |
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