Thomas Oellerich, Constanze Schneider, Dominique Jeanette Thomas, Kirsten M. Knecht, Olga Buzovetsky, Lars Kaderali, Christoph Schliemann, Hanibal Bohnenberger, Linus Angenendt, Wolfgang Hartmann, Eva Wardelmann, Tamara Rothenburger, Sebastian Mohr, Sebastian Scheich, Federico Comoglio, Anne Wilke, Philipp Ströbel, Hubert Serve, Martin Michaelis, Nerea Ferreirós Bouzas, Gerd Geisslinger, Yong Xiong, Oliver Till Keppler, Jindrich Cinatl
- Hypomethylating agents decitabine and azacytidine are regarded as interchangeable in the treatment of acute myeloid leukemia (AML). However, their mechanisms of action remain incompletely understood, and predictive biomarkers for HMA efficacy are lacking. Here, we show that the bioactive metabolite decitabine triphosphate, but not azacytidine triphosphate, functions as activator and substrate of the triphosphohydrolase SAMHD1 and is subject to SAMHD1-mediated inactivation. Retrospective immunohistochemical analysis of bone marrow specimens from AML patients at diagnosis revealed that SAMHD1 expression in leukemic cells inversely correlates with clinical response to decitabine, but not to azacytidine. SAMHD1 ablation increases the antileukemic activity of decitabine in AML cell lines, primary leukemic blasts, and xenograft models. AML cells acquire resistance to decitabine partly by SAMHD1 up-regulation. Together, our data suggest that SAMHD1 is a biomarker for the stratified use of hypomethylating agents in AML patients and a potential target for the treatment of decitabine-resistant leukemia.
MetadatenVerfasserangaben: | Thomas OellerichORCiD, Constanze SchneiderGND, Dominique Jeanette ThomasORCiDGND, Kirsten M. KnechtORCiD, Olga Buzovetsky, Lars KaderaliORCiDGND, Christoph Schliemann, Hanibal BohnenbergerORCiD, Linus AngenendtORCiDGND, Wolfgang HartmannORCiDGND, Eva WardelmannORCiDGND, Tamara RothenburgerORCiD, Sebastian Mohr, Sebastian ScheichORCiD, Federico ComoglioORCiDGND, Anne Wilke, Philipp Ströbel, Hubert ServeORCiDGND, Martin MichaelisORCiDGND, Nerea Ferreirós BouzasORCiDGND, Gerd GeisslingerORCiDGND, Yong XiongORCiD, Oliver Till KepplerORCiDGND, Jindrich CinatlORCiDGND |
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URN: | urn:nbn:de:hebis:30:3-507543 |
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DOI: | https://doi.org/10.1038/s41467-019-11413-4 |
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ISSN: | 2041-1723 |
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Pubmed-Id: | https://pubmed.ncbi.nlm.nih.gov/31375673 |
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Titel des übergeordneten Werkes (Englisch): | Nature Communications |
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Verlag: | Nature Publishing Group UK |
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Verlagsort: | [London] |
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Dokumentart: | Wissenschaftlicher Artikel |
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Sprache: | Englisch |
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Jahr der Fertigstellung: | 2019 |
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Datum der Erstveröffentlichung: | 02.08.2019 |
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Veröffentlichende Institution: | Universitätsbibliothek Johann Christian Senckenberg |
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Datum der Freischaltung: | 19.08.2019 |
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Freies Schlagwort / Tag: | Biomarkers; Cancer; Oncology |
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Jahrgang: | 10 |
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Ausgabe / Heft: | 1, Art. 3475 |
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Seitenzahl: | 14 |
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Erste Seite: | 1 |
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Letzte Seite: | 14 |
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Bemerkung: | 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
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HeBIS-PPN: | 453739636 |
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Institute: | Medizin / Medizin |
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DDC-Klassifikation: | 6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit |
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Sammlungen: | Universitätspublikationen |
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Lizenz (Deutsch): | Creative Commons - Namensnennung 4.0 |
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