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Genome-wide DNA methylation analysis pre- and post-lenalidomide treatment in patients with myelodysplastic syndrome with isolated deletion (5q)
Myelodysplastic syndrome (MDS) with isolated deletion of chromosome 5q (MDS del5q) is a distinct subtype of MDS with quite favorable prognosis and excellent response to treatment with lenalidomide. Still, a relevant percentage of patients do not respond to lenalidomide and even experience progressio...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116243/ https://www.ncbi.nlm.nih.gov/pubmed/33903952 http://dx.doi.org/10.1007/s00277-021-04492-1 |
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author | Hecht, Anna Meyer, Julia A. Jann, Johann-Christoph Sockel, Katja Giagounidis, Aristoteles Götze, Katharina S. Letsch, Anne Haase, Detlef Schlenk, Richard F. Haferlach, Torsten Schafhausen, Philippe Bug, Gesine Lübbert, Michael Thol, Felicitas Büsche, Guntram Schuler, Esther Nowak, Verena Obländer, Julia Fey, Stephanie Müller, Nadine Metzgeroth, Georgia Hofmann, Wolf-Karsten Germing, Ulrich Nolte, Florian Reinwald, Mark Nowak, Daniel |
author_facet | Hecht, Anna Meyer, Julia A. Jann, Johann-Christoph Sockel, Katja Giagounidis, Aristoteles Götze, Katharina S. Letsch, Anne Haase, Detlef Schlenk, Richard F. Haferlach, Torsten Schafhausen, Philippe Bug, Gesine Lübbert, Michael Thol, Felicitas Büsche, Guntram Schuler, Esther Nowak, Verena Obländer, Julia Fey, Stephanie Müller, Nadine Metzgeroth, Georgia Hofmann, Wolf-Karsten Germing, Ulrich Nolte, Florian Reinwald, Mark Nowak, Daniel |
author_sort | Hecht, Anna |
collection | PubMed |
description | Myelodysplastic syndrome (MDS) with isolated deletion of chromosome 5q (MDS del5q) is a distinct subtype of MDS with quite favorable prognosis and excellent response to treatment with lenalidomide. Still, a relevant percentage of patients do not respond to lenalidomide and even experience progression to acute myeloid leukemia (AML). In this study, we aimed to investigate whether global DNA methylation patterns could predict response to lenalidomide. Genome-wide DNA methylation analysis using Illumina 450k methylation arrays was performed on n=51 patients with MDS del5q who were uniformly treated with lenalidomide in a prospective multicenter trial of the German MDS study group. To study potential direct effects of lenalidomide on DNA methylation, 17 paired samples pre- and post-treatment were analyzed. Our results revealed no relevant effect of lenalidomide on methylation status. Furthermore, methylation patterns prior to therapy could not predict lenalidomide response. However, methylation clustering identified a group of patients with a trend towards inferior overall survival. These patients showed hypermethylation of several interesting target genes, including genes of relevant signaling pathways, potentially indicating the evaluation of novel therapeutic targets. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00277-021-04492-1. |
format | Online Article Text |
id | pubmed-8116243 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-81162432021-05-13 Genome-wide DNA methylation analysis pre- and post-lenalidomide treatment in patients with myelodysplastic syndrome with isolated deletion (5q) Hecht, Anna Meyer, Julia A. Jann, Johann-Christoph Sockel, Katja Giagounidis, Aristoteles Götze, Katharina S. Letsch, Anne Haase, Detlef Schlenk, Richard F. Haferlach, Torsten Schafhausen, Philippe Bug, Gesine Lübbert, Michael Thol, Felicitas Büsche, Guntram Schuler, Esther Nowak, Verena Obländer, Julia Fey, Stephanie Müller, Nadine Metzgeroth, Georgia Hofmann, Wolf-Karsten Germing, Ulrich Nolte, Florian Reinwald, Mark Nowak, Daniel Ann Hematol Original Article Myelodysplastic syndrome (MDS) with isolated deletion of chromosome 5q (MDS del5q) is a distinct subtype of MDS with quite favorable prognosis and excellent response to treatment with lenalidomide. Still, a relevant percentage of patients do not respond to lenalidomide and even experience progression to acute myeloid leukemia (AML). In this study, we aimed to investigate whether global DNA methylation patterns could predict response to lenalidomide. Genome-wide DNA methylation analysis using Illumina 450k methylation arrays was performed on n=51 patients with MDS del5q who were uniformly treated with lenalidomide in a prospective multicenter trial of the German MDS study group. To study potential direct effects of lenalidomide on DNA methylation, 17 paired samples pre- and post-treatment were analyzed. Our results revealed no relevant effect of lenalidomide on methylation status. Furthermore, methylation patterns prior to therapy could not predict lenalidomide response. However, methylation clustering identified a group of patients with a trend towards inferior overall survival. These patients showed hypermethylation of several interesting target genes, including genes of relevant signaling pathways, potentially indicating the evaluation of novel therapeutic targets. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00277-021-04492-1. Springer Berlin Heidelberg 2021-04-27 2021 /pmc/articles/PMC8116243/ /pubmed/33903952 http://dx.doi.org/10.1007/s00277-021-04492-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Hecht, Anna Meyer, Julia A. Jann, Johann-Christoph Sockel, Katja Giagounidis, Aristoteles Götze, Katharina S. Letsch, Anne Haase, Detlef Schlenk, Richard F. Haferlach, Torsten Schafhausen, Philippe Bug, Gesine Lübbert, Michael Thol, Felicitas Büsche, Guntram Schuler, Esther Nowak, Verena Obländer, Julia Fey, Stephanie Müller, Nadine Metzgeroth, Georgia Hofmann, Wolf-Karsten Germing, Ulrich Nolte, Florian Reinwald, Mark Nowak, Daniel Genome-wide DNA methylation analysis pre- and post-lenalidomide treatment in patients with myelodysplastic syndrome with isolated deletion (5q) |
title | Genome-wide DNA methylation analysis pre- and post-lenalidomide treatment in patients with myelodysplastic syndrome with isolated deletion (5q) |
title_full | Genome-wide DNA methylation analysis pre- and post-lenalidomide treatment in patients with myelodysplastic syndrome with isolated deletion (5q) |
title_fullStr | Genome-wide DNA methylation analysis pre- and post-lenalidomide treatment in patients with myelodysplastic syndrome with isolated deletion (5q) |
title_full_unstemmed | Genome-wide DNA methylation analysis pre- and post-lenalidomide treatment in patients with myelodysplastic syndrome with isolated deletion (5q) |
title_short | Genome-wide DNA methylation analysis pre- and post-lenalidomide treatment in patients with myelodysplastic syndrome with isolated deletion (5q) |
title_sort | genome-wide dna methylation analysis pre- and post-lenalidomide treatment in patients with myelodysplastic syndrome with isolated deletion (5q) |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116243/ https://www.ncbi.nlm.nih.gov/pubmed/33903952 http://dx.doi.org/10.1007/s00277-021-04492-1 |
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