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DNA methylation at an enhancer of the three prime repair exonuclease 2 gene (TREX2) is linked to gene expression and survival in laryngeal cancer
BACKGROUND: Genetic aberrations in DNA repair genes are linked to cancer, but less is reported about epigenetic regulation of DNA repair and functional consequences. We investigated the intragenic methylation loss at the three prime repair exonuclease 2 (TREX2) locus in laryngeal (n = 256) and color...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6499986/ https://www.ncbi.nlm.nih.gov/pubmed/31053176 http://dx.doi.org/10.1186/s13148-019-0666-5 |
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author | Weigel, Christoph Chaisaingmongkol, Jittiporn Assenov, Yassen Kuhmann, Christine Winkler, Volker Santi, Irene Bogatyrova, Olga Kaucher, Simone Bermejo, Justo L. Leung, Suet Y. Chan, Tsun L. Lasitschka, Felix Bohrer, Manfred H. Marx, Alexander Haußen, Roland Heyny-von Herold-Mende, Christel Dyckhoff, Gerhard Boukamp, Petra Delank, Klaus W. Hörmann, Karl Lippert, Burkhard M. Baier, Gerald Dietz, Andreas Oakes, Christopher C. Plass, Christoph Becher, Heiko Schmezer, Peter Ramroth, Heribert Popanda, Odilia |
author_facet | Weigel, Christoph Chaisaingmongkol, Jittiporn Assenov, Yassen Kuhmann, Christine Winkler, Volker Santi, Irene Bogatyrova, Olga Kaucher, Simone Bermejo, Justo L. Leung, Suet Y. Chan, Tsun L. Lasitschka, Felix Bohrer, Manfred H. Marx, Alexander Haußen, Roland Heyny-von Herold-Mende, Christel Dyckhoff, Gerhard Boukamp, Petra Delank, Klaus W. Hörmann, Karl Lippert, Burkhard M. Baier, Gerald Dietz, Andreas Oakes, Christopher C. Plass, Christoph Becher, Heiko Schmezer, Peter Ramroth, Heribert Popanda, Odilia |
author_sort | Weigel, Christoph |
collection | PubMed |
description | BACKGROUND: Genetic aberrations in DNA repair genes are linked to cancer, but less is reported about epigenetic regulation of DNA repair and functional consequences. We investigated the intragenic methylation loss at the three prime repair exonuclease 2 (TREX2) locus in laryngeal (n = 256) and colorectal cancer cases (n = 95) and in pan-cancer data from The Cancer Genome Atlas (TCGA). RESULTS: Significant methylation loss at an intragenic site of TREX2 was a frequent trait in both patient cohorts (p = 0.016 and < 0.001, respectively) and in 15 out of 22 TCGA studies. Methylation loss correlated with immunohistochemically staining for TREX2 (p < 0.0001) in laryngeal tumors and improved overall survival of laryngeal cancer patients (p = 0.045). Chromatin immunoprecipitation, demethylation experiments, and reporter gene assays revealed that the region of methylation loss can function as a CCAAT/enhancer binding protein alpha (CEBPA)-responsive enhancer element regulating TREX2 expression. CONCLUSIONS: The data highlight a regulatory role of TREX2 DNA methylation for gene expression which might affect incidence and survival of laryngeal cancer. Altered TREX2 protein levels in tumors may affect drug-induced DNA damage repair and provide new tailored therapies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13148-019-0666-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6499986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64999862019-05-09 DNA methylation at an enhancer of the three prime repair exonuclease 2 gene (TREX2) is linked to gene expression and survival in laryngeal cancer Weigel, Christoph Chaisaingmongkol, Jittiporn Assenov, Yassen Kuhmann, Christine Winkler, Volker Santi, Irene Bogatyrova, Olga Kaucher, Simone Bermejo, Justo L. Leung, Suet Y. Chan, Tsun L. Lasitschka, Felix Bohrer, Manfred H. Marx, Alexander Haußen, Roland Heyny-von Herold-Mende, Christel Dyckhoff, Gerhard Boukamp, Petra Delank, Klaus W. Hörmann, Karl Lippert, Burkhard M. Baier, Gerald Dietz, Andreas Oakes, Christopher C. Plass, Christoph Becher, Heiko Schmezer, Peter Ramroth, Heribert Popanda, Odilia Clin Epigenetics Research BACKGROUND: Genetic aberrations in DNA repair genes are linked to cancer, but less is reported about epigenetic regulation of DNA repair and functional consequences. We investigated the intragenic methylation loss at the three prime repair exonuclease 2 (TREX2) locus in laryngeal (n = 256) and colorectal cancer cases (n = 95) and in pan-cancer data from The Cancer Genome Atlas (TCGA). RESULTS: Significant methylation loss at an intragenic site of TREX2 was a frequent trait in both patient cohorts (p = 0.016 and < 0.001, respectively) and in 15 out of 22 TCGA studies. Methylation loss correlated with immunohistochemically staining for TREX2 (p < 0.0001) in laryngeal tumors and improved overall survival of laryngeal cancer patients (p = 0.045). Chromatin immunoprecipitation, demethylation experiments, and reporter gene assays revealed that the region of methylation loss can function as a CCAAT/enhancer binding protein alpha (CEBPA)-responsive enhancer element regulating TREX2 expression. CONCLUSIONS: The data highlight a regulatory role of TREX2 DNA methylation for gene expression which might affect incidence and survival of laryngeal cancer. Altered TREX2 protein levels in tumors may affect drug-induced DNA damage repair and provide new tailored therapies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13148-019-0666-5) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-03 /pmc/articles/PMC6499986/ /pubmed/31053176 http://dx.doi.org/10.1186/s13148-019-0666-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Weigel, Christoph Chaisaingmongkol, Jittiporn Assenov, Yassen Kuhmann, Christine Winkler, Volker Santi, Irene Bogatyrova, Olga Kaucher, Simone Bermejo, Justo L. Leung, Suet Y. Chan, Tsun L. Lasitschka, Felix Bohrer, Manfred H. Marx, Alexander Haußen, Roland Heyny-von Herold-Mende, Christel Dyckhoff, Gerhard Boukamp, Petra Delank, Klaus W. Hörmann, Karl Lippert, Burkhard M. Baier, Gerald Dietz, Andreas Oakes, Christopher C. Plass, Christoph Becher, Heiko Schmezer, Peter Ramroth, Heribert Popanda, Odilia DNA methylation at an enhancer of the three prime repair exonuclease 2 gene (TREX2) is linked to gene expression and survival in laryngeal cancer |
title | DNA methylation at an enhancer of the three prime repair exonuclease 2 gene (TREX2) is linked to gene expression and survival in laryngeal cancer |
title_full | DNA methylation at an enhancer of the three prime repair exonuclease 2 gene (TREX2) is linked to gene expression and survival in laryngeal cancer |
title_fullStr | DNA methylation at an enhancer of the three prime repair exonuclease 2 gene (TREX2) is linked to gene expression and survival in laryngeal cancer |
title_full_unstemmed | DNA methylation at an enhancer of the three prime repair exonuclease 2 gene (TREX2) is linked to gene expression and survival in laryngeal cancer |
title_short | DNA methylation at an enhancer of the three prime repair exonuclease 2 gene (TREX2) is linked to gene expression and survival in laryngeal cancer |
title_sort | dna methylation at an enhancer of the three prime repair exonuclease 2 gene (trex2) is linked to gene expression and survival in laryngeal cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6499986/ https://www.ncbi.nlm.nih.gov/pubmed/31053176 http://dx.doi.org/10.1186/s13148-019-0666-5 |
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