The BLIMP1—EZH2 nexus in a non-Hodgkin lymphoma

Funding Information: Funding This work was supported by project grants from the Icelandic Research Fund (grant no. 140950-051) and the Icelandic Cancer Society, a doctoral fellowship from the University of Iceland, and grant from the University of Iceland Eggertssjodur and funds from the COST Projec...

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Published in:Oncogene
Main Authors: Harðardóttir, Ingibjörg, Anderson, Kimberley Jade, Ósvaldsdóttir, Árný Björg, Atzinger, Birgit, Traustadóttir, Gunnhildur Ásta, Jensen, Kirstine Nolling, Lárusdóttir, Aðalheiður Elín, Bergþórsson, Jón Þór, Magnúsdóttir, Erna
Other Authors: Clinical Laboratory Services, Diagnostics and Blood Bank, Faculty of Medicine, Landspitali - The National University Hospital of Iceland, University of Iceland
Format: Article in Journal/Newspaper
Language:English
Published: 2020
Subjects:
Online Access:https://hdl.handle.net/20.500.11815/3611
https://doi.org/10.1038/s41388-020-1347-8
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spelling ftopinvisindi:oai:opinvisindi.is:20.500.11815/3611 2023-11-12T04:19:13+01:00 The BLIMP1—EZH2 nexus in a non-Hodgkin lymphoma Harðardóttir, Ingibjörg Anderson, Kimberley Jade Ósvaldsdóttir, Árný Björg Atzinger, Birgit Traustadóttir, Gunnhildur Ásta Jensen, Kirstine Nolling Lárusdóttir, Aðalheiður Elín Bergþórsson, Jón Þór Magnúsdóttir, Erna Clinical Laboratory Services, Diagnostics and Blood Bank Faculty of Medicine Landspitali - The National University Hospital of Iceland University of Iceland 2020-07-09 14 6011306 5138-5151 https://hdl.handle.net/20.500.11815/3611 https://doi.org/10.1038/s41388-020-1347-8 en eng Oncogene; 39(28) http://www.scopus.com/inward/record.url?scp=85086372286&partnerID=8YFLogxK Harðardóttir , I , Anderson , K J , Ósvaldsdóttir , Á B , Atzinger , B , Traustadóttir , G Á , Jensen , K N , Lárusdóttir , A E , Bergþórsson , J Þ & Magnúsdóttir , E 2020 , ' The BLIMP1—EZH2 nexus in a non-Hodgkin lymphoma ' , Oncogene , vol. 39 , no. 28 , pp. 5138-5151 . https://doi.org/10.1038/s41388-020-1347-8 0950-9232 60292600 cfbabd04-975f-4b58-bf51-2224b8ca142f ORCID: /0000-0003-0178-7047/work/115075535 32533097 85086372286 https://hdl.handle.net/20.500.11815/3611 doi:10.1038/s41388-020-1347-8 info:eu-repo/semantics/openAccess Náttúrufræðingar Molecular Biology Genetics Cancer Research /dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/article 2020 ftopinvisindi https://doi.org/20.500.11815/361110.1038/s41388-020-1347-8 2023-11-01T23:55:24Z Funding Information: Funding This work was supported by project grants from the Icelandic Research Fund (grant no. 140950-051) and the Icelandic Cancer Society, a doctoral fellowship from the University of Iceland, and grant from the University of Iceland Eggertssjodur and funds from the COST Project EpiChemBio. Publisher Copyright: © 2020, The Author(s), under exclusive licence to Springer Nature Limited. Waldenström’s macroglobulinemia (WM) is a non-Hodgkin lymphoma, resulting in antibody-secreting lymphoplasmacytic cells in the bone marrow and pathologies resulting from high levels of monoclonal immunoglobulin M (IgM) in the blood. Despite the key role for BLIMP1 in plasma cell maturation and antibody secretion, its potential effect on WM cell biology has not yet been explored. Here we provide evidence of a crucial role for BLIMP1 in the survival of cells from WM cell line models and further demonstrate that BLIMP1 is necessary for the expression of the histone methyltransferase EZH2 in both WM and multiple myeloma cell lines. The effect of BLIMP1 on EZH2 levels is post-translational, at least partially through the regulation of proteasomal targeting of EZH2. Chromatin immunoprecipitation analysis and transcriptome profiling suggest that the two factors co-operate in regulating genes involved in cancer cell immune evasion. Co-cultures of natural killer cells and cells from a WM cell line further suggest that both factors participate in immune evasion by promoting escape from natural killer cell-mediated cytotoxicity. Together, the interplay of BLIMP1 and EZH2 plays a vital role in promoting the survival of WM cell lines, suggesting a role for the two factors in Waldenström’s macroglobulinaemia. Peer reviewed Article in Journal/Newspaper Iceland Opin vísindi (Iceland) Oncogene 39 28 5138 5151
institution Open Polar
collection Opin vísindi (Iceland)
op_collection_id ftopinvisindi
language English
topic Náttúrufræðingar
Molecular Biology
Genetics
Cancer Research
spellingShingle Náttúrufræðingar
Molecular Biology
Genetics
Cancer Research
Harðardóttir, Ingibjörg
Anderson, Kimberley Jade
Ósvaldsdóttir, Árný Björg
Atzinger, Birgit
Traustadóttir, Gunnhildur Ásta
Jensen, Kirstine Nolling
Lárusdóttir, Aðalheiður Elín
Bergþórsson, Jón Þór
Magnúsdóttir, Erna
The BLIMP1—EZH2 nexus in a non-Hodgkin lymphoma
topic_facet Náttúrufræðingar
Molecular Biology
Genetics
Cancer Research
description Funding Information: Funding This work was supported by project grants from the Icelandic Research Fund (grant no. 140950-051) and the Icelandic Cancer Society, a doctoral fellowship from the University of Iceland, and grant from the University of Iceland Eggertssjodur and funds from the COST Project EpiChemBio. Publisher Copyright: © 2020, The Author(s), under exclusive licence to Springer Nature Limited. Waldenström’s macroglobulinemia (WM) is a non-Hodgkin lymphoma, resulting in antibody-secreting lymphoplasmacytic cells in the bone marrow and pathologies resulting from high levels of monoclonal immunoglobulin M (IgM) in the blood. Despite the key role for BLIMP1 in plasma cell maturation and antibody secretion, its potential effect on WM cell biology has not yet been explored. Here we provide evidence of a crucial role for BLIMP1 in the survival of cells from WM cell line models and further demonstrate that BLIMP1 is necessary for the expression of the histone methyltransferase EZH2 in both WM and multiple myeloma cell lines. The effect of BLIMP1 on EZH2 levels is post-translational, at least partially through the regulation of proteasomal targeting of EZH2. Chromatin immunoprecipitation analysis and transcriptome profiling suggest that the two factors co-operate in regulating genes involved in cancer cell immune evasion. Co-cultures of natural killer cells and cells from a WM cell line further suggest that both factors participate in immune evasion by promoting escape from natural killer cell-mediated cytotoxicity. Together, the interplay of BLIMP1 and EZH2 plays a vital role in promoting the survival of WM cell lines, suggesting a role for the two factors in Waldenström’s macroglobulinaemia. Peer reviewed
author2 Clinical Laboratory Services, Diagnostics and Blood Bank
Faculty of Medicine
Landspitali - The National University Hospital of Iceland
University of Iceland
format Article in Journal/Newspaper
author Harðardóttir, Ingibjörg
Anderson, Kimberley Jade
Ósvaldsdóttir, Árný Björg
Atzinger, Birgit
Traustadóttir, Gunnhildur Ásta
Jensen, Kirstine Nolling
Lárusdóttir, Aðalheiður Elín
Bergþórsson, Jón Þór
Magnúsdóttir, Erna
author_facet Harðardóttir, Ingibjörg
Anderson, Kimberley Jade
Ósvaldsdóttir, Árný Björg
Atzinger, Birgit
Traustadóttir, Gunnhildur Ásta
Jensen, Kirstine Nolling
Lárusdóttir, Aðalheiður Elín
Bergþórsson, Jón Þór
Magnúsdóttir, Erna
author_sort Harðardóttir, Ingibjörg
title The BLIMP1—EZH2 nexus in a non-Hodgkin lymphoma
title_short The BLIMP1—EZH2 nexus in a non-Hodgkin lymphoma
title_full The BLIMP1—EZH2 nexus in a non-Hodgkin lymphoma
title_fullStr The BLIMP1—EZH2 nexus in a non-Hodgkin lymphoma
title_full_unstemmed The BLIMP1—EZH2 nexus in a non-Hodgkin lymphoma
title_sort blimp1—ezh2 nexus in a non-hodgkin lymphoma
publishDate 2020
url https://hdl.handle.net/20.500.11815/3611
https://doi.org/10.1038/s41388-020-1347-8
genre Iceland
genre_facet Iceland
op_relation Oncogene; 39(28)
http://www.scopus.com/inward/record.url?scp=85086372286&partnerID=8YFLogxK
Harðardóttir , I , Anderson , K J , Ósvaldsdóttir , Á B , Atzinger , B , Traustadóttir , G Á , Jensen , K N , Lárusdóttir , A E , Bergþórsson , J Þ & Magnúsdóttir , E 2020 , ' The BLIMP1—EZH2 nexus in a non-Hodgkin lymphoma ' , Oncogene , vol. 39 , no. 28 , pp. 5138-5151 . https://doi.org/10.1038/s41388-020-1347-8
0950-9232
60292600
cfbabd04-975f-4b58-bf51-2224b8ca142f
ORCID: /0000-0003-0178-7047/work/115075535
32533097
85086372286
https://hdl.handle.net/20.500.11815/3611
doi:10.1038/s41388-020-1347-8
op_rights info:eu-repo/semantics/openAccess
op_doi https://doi.org/20.500.11815/361110.1038/s41388-020-1347-8
container_title Oncogene
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