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The histone demethylase JMJD2C constitutes a novel NFE2 target gene that is required for the survival of JAK2(V617F) mutated cells

The transcription factor NFE2 is overexpressed in most patients with myeloproliferative neoplasms (MPN). Moreover, mutations in NFE2, found in a subset of MPN patients, strongly predispose for transformation to acute leukemia. Transgenic mice overexpressing NFE2 as well as mice harboring NFE2 mutati...

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Autores principales: Staehle, Anne Marie, Peeken, Jan Caspar, Vladimirov, Georg, Hoeness, Mirjam Elisabeth, Bojtine Kovacs, Sarolta, Karantzelis, Nikolaos, Gruender, Albert, Koellerer, Christoph, Jutzi, Jonas Samuel, Pahl, Heike Luise, Staehle, Hans Felix
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10079541/
https://www.ncbi.nlm.nih.gov/pubmed/36709354
http://dx.doi.org/10.1038/s41375-023-01826-y
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author Staehle, Anne Marie
Peeken, Jan Caspar
Vladimirov, Georg
Hoeness, Mirjam Elisabeth
Bojtine Kovacs, Sarolta
Karantzelis, Nikolaos
Gruender, Albert
Koellerer, Christoph
Jutzi, Jonas Samuel
Pahl, Heike Luise
Staehle, Hans Felix
author_facet Staehle, Anne Marie
Peeken, Jan Caspar
Vladimirov, Georg
Hoeness, Mirjam Elisabeth
Bojtine Kovacs, Sarolta
Karantzelis, Nikolaos
Gruender, Albert
Koellerer, Christoph
Jutzi, Jonas Samuel
Pahl, Heike Luise
Staehle, Hans Felix
author_sort Staehle, Anne Marie
collection PubMed
description The transcription factor NFE2 is overexpressed in most patients with myeloproliferative neoplasms (MPN). Moreover, mutations in NFE2, found in a subset of MPN patients, strongly predispose for transformation to acute leukemia. Transgenic mice overexpressing NFE2 as well as mice harboring NFE2 mutations display an MPN phenotype and spontaneously develop leukemia. However, the molecular mechanisms effecting NFE2-driven leukemic transformation remain incompletely understood. Here we show that the pro-leukemic histone demethylase JMJD2C constitutes a novel NFE2 target gene. JMJD2C expression is elevated in MPN patients as well as in NFE2 transgenic mice. Moreover, we show that loss of JMJD2C selectively impairs proliferation of JAK2(V617F) mutated cells. Our data suggest that JMJD2C represents a promising drug target in MPN and provide a rationale for further investigation in preclinical and clinical settings.
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spelling pubmed-100795412023-04-08 The histone demethylase JMJD2C constitutes a novel NFE2 target gene that is required for the survival of JAK2(V617F) mutated cells Staehle, Anne Marie Peeken, Jan Caspar Vladimirov, Georg Hoeness, Mirjam Elisabeth Bojtine Kovacs, Sarolta Karantzelis, Nikolaos Gruender, Albert Koellerer, Christoph Jutzi, Jonas Samuel Pahl, Heike Luise Staehle, Hans Felix Leukemia Letter The transcription factor NFE2 is overexpressed in most patients with myeloproliferative neoplasms (MPN). Moreover, mutations in NFE2, found in a subset of MPN patients, strongly predispose for transformation to acute leukemia. Transgenic mice overexpressing NFE2 as well as mice harboring NFE2 mutations display an MPN phenotype and spontaneously develop leukemia. However, the molecular mechanisms effecting NFE2-driven leukemic transformation remain incompletely understood. Here we show that the pro-leukemic histone demethylase JMJD2C constitutes a novel NFE2 target gene. JMJD2C expression is elevated in MPN patients as well as in NFE2 transgenic mice. Moreover, we show that loss of JMJD2C selectively impairs proliferation of JAK2(V617F) mutated cells. Our data suggest that JMJD2C represents a promising drug target in MPN and provide a rationale for further investigation in preclinical and clinical settings. Nature Publishing Group UK 2023-01-28 2023 /pmc/articles/PMC10079541/ /pubmed/36709354 http://dx.doi.org/10.1038/s41375-023-01826-y Text en © The Author(s) 2023 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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Letter
Staehle, Anne Marie
Peeken, Jan Caspar
Vladimirov, Georg
Hoeness, Mirjam Elisabeth
Bojtine Kovacs, Sarolta
Karantzelis, Nikolaos
Gruender, Albert
Koellerer, Christoph
Jutzi, Jonas Samuel
Pahl, Heike Luise
Staehle, Hans Felix
The histone demethylase JMJD2C constitutes a novel NFE2 target gene that is required for the survival of JAK2(V617F) mutated cells
title The histone demethylase JMJD2C constitutes a novel NFE2 target gene that is required for the survival of JAK2(V617F) mutated cells
title_full The histone demethylase JMJD2C constitutes a novel NFE2 target gene that is required for the survival of JAK2(V617F) mutated cells
title_fullStr The histone demethylase JMJD2C constitutes a novel NFE2 target gene that is required for the survival of JAK2(V617F) mutated cells
title_full_unstemmed The histone demethylase JMJD2C constitutes a novel NFE2 target gene that is required for the survival of JAK2(V617F) mutated cells
title_short The histone demethylase JMJD2C constitutes a novel NFE2 target gene that is required for the survival of JAK2(V617F) mutated cells
title_sort histone demethylase jmjd2c constitutes a novel nfe2 target gene that is required for the survival of jak2(v617f) mutated cells
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10079541/
https://www.ncbi.nlm.nih.gov/pubmed/36709354
http://dx.doi.org/10.1038/s41375-023-01826-y
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