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Amplification of 9p24.1 in diffuse large B-cell lymphoma identifies a unique subset of cases that resemble primary mediastinal large B-cell lymphoma
Copy number alterations (CNAs) of 9p24.1 occur frequently in Hodgkin lymphoma, primary mediastinal large B-cell lymphoma (PMBCL), primary central nervous system lymphoma, and primary testicular lymphoma, resulting in overexpression of PD-L1 and sensitivity to PD-1 blockade-based immunotherapy. While...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717207/ https://www.ncbi.nlm.nih.gov/pubmed/31471540 http://dx.doi.org/10.1038/s41408-019-0233-5 |
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author | Wang, Yucai Wenzl, Kerstin Manske, Michelle K. Asmann, Yan W. Sarangi, Vivekananda Greipp, Patricia T. Krull, Jordan E. Hartert, Keenan He, Rong Feldman, Andrew L. Maurer, Matthew J. Slager, Susan L. Nowakowski, Grzegorz S. Habermann, Thomas M. Witzig, Thomas E. Link, Brian K. Ansell, Stephen M. Cerhan, James R. Novak, Anne J. |
author_facet | Wang, Yucai Wenzl, Kerstin Manske, Michelle K. Asmann, Yan W. Sarangi, Vivekananda Greipp, Patricia T. Krull, Jordan E. Hartert, Keenan He, Rong Feldman, Andrew L. Maurer, Matthew J. Slager, Susan L. Nowakowski, Grzegorz S. Habermann, Thomas M. Witzig, Thomas E. Link, Brian K. Ansell, Stephen M. Cerhan, James R. Novak, Anne J. |
author_sort | Wang, Yucai |
collection | PubMed |
description | Copy number alterations (CNAs) of 9p24.1 occur frequently in Hodgkin lymphoma, primary mediastinal large B-cell lymphoma (PMBCL), primary central nervous system lymphoma, and primary testicular lymphoma, resulting in overexpression of PD-L1 and sensitivity to PD-1 blockade-based immunotherapy. While 9p24.1 CNA was also reported in diffuse large B-cell lymphoma (DLBCL), little is known about its molecular or clinical significance. In this study, we analyzed the prevalence of 9p24.1 CNA in newly diagnosed DLBCL and examined its association with PD-L1, PD-L2, and JAK2 expression, clinical characteristics, and outcome. We found that 10% of DLBCL cases had CNA of 9p24.1, with 6.5% gains, and 3.5% amplifications. Only the cases with a 9p24.1 amplification had high levels of PD-L1, PD-L2, and JAK2 expression. Gains or amplifications of 9p24.1 were associated with a younger age and the ABC/non-GCB subtype. Compared with DLBCL cases without 9p24.1 CNA, the cases with a 9p24.1 amplification had a trend of better event-free survival. Furthermore, the amplification cases had a gene expression and mutation profile similar to those of PMBCL. Our data suggest that amplification of 9p24.1 identifies a unique subset of DLBCL with clinical and molecular features resembling PMBCL that may be amenable to PD-1 blockade-based immunotherapy. |
format | Online Article Text |
id | pubmed-6717207 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67172072019-09-03 Amplification of 9p24.1 in diffuse large B-cell lymphoma identifies a unique subset of cases that resemble primary mediastinal large B-cell lymphoma Wang, Yucai Wenzl, Kerstin Manske, Michelle K. Asmann, Yan W. Sarangi, Vivekananda Greipp, Patricia T. Krull, Jordan E. Hartert, Keenan He, Rong Feldman, Andrew L. Maurer, Matthew J. Slager, Susan L. Nowakowski, Grzegorz S. Habermann, Thomas M. Witzig, Thomas E. Link, Brian K. Ansell, Stephen M. Cerhan, James R. Novak, Anne J. Blood Cancer J Article Copy number alterations (CNAs) of 9p24.1 occur frequently in Hodgkin lymphoma, primary mediastinal large B-cell lymphoma (PMBCL), primary central nervous system lymphoma, and primary testicular lymphoma, resulting in overexpression of PD-L1 and sensitivity to PD-1 blockade-based immunotherapy. While 9p24.1 CNA was also reported in diffuse large B-cell lymphoma (DLBCL), little is known about its molecular or clinical significance. In this study, we analyzed the prevalence of 9p24.1 CNA in newly diagnosed DLBCL and examined its association with PD-L1, PD-L2, and JAK2 expression, clinical characteristics, and outcome. We found that 10% of DLBCL cases had CNA of 9p24.1, with 6.5% gains, and 3.5% amplifications. Only the cases with a 9p24.1 amplification had high levels of PD-L1, PD-L2, and JAK2 expression. Gains or amplifications of 9p24.1 were associated with a younger age and the ABC/non-GCB subtype. Compared with DLBCL cases without 9p24.1 CNA, the cases with a 9p24.1 amplification had a trend of better event-free survival. Furthermore, the amplification cases had a gene expression and mutation profile similar to those of PMBCL. Our data suggest that amplification of 9p24.1 identifies a unique subset of DLBCL with clinical and molecular features resembling PMBCL that may be amenable to PD-1 blockade-based immunotherapy. Nature Publishing Group UK 2019-08-30 /pmc/articles/PMC6717207/ /pubmed/31471540 http://dx.doi.org/10.1038/s41408-019-0233-5 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Wang, Yucai Wenzl, Kerstin Manske, Michelle K. Asmann, Yan W. Sarangi, Vivekananda Greipp, Patricia T. Krull, Jordan E. Hartert, Keenan He, Rong Feldman, Andrew L. Maurer, Matthew J. Slager, Susan L. Nowakowski, Grzegorz S. Habermann, Thomas M. Witzig, Thomas E. Link, Brian K. Ansell, Stephen M. Cerhan, James R. Novak, Anne J. Amplification of 9p24.1 in diffuse large B-cell lymphoma identifies a unique subset of cases that resemble primary mediastinal large B-cell lymphoma |
title | Amplification of 9p24.1 in diffuse large B-cell lymphoma identifies a unique subset of cases that resemble primary mediastinal large B-cell lymphoma |
title_full | Amplification of 9p24.1 in diffuse large B-cell lymphoma identifies a unique subset of cases that resemble primary mediastinal large B-cell lymphoma |
title_fullStr | Amplification of 9p24.1 in diffuse large B-cell lymphoma identifies a unique subset of cases that resemble primary mediastinal large B-cell lymphoma |
title_full_unstemmed | Amplification of 9p24.1 in diffuse large B-cell lymphoma identifies a unique subset of cases that resemble primary mediastinal large B-cell lymphoma |
title_short | Amplification of 9p24.1 in diffuse large B-cell lymphoma identifies a unique subset of cases that resemble primary mediastinal large B-cell lymphoma |
title_sort | amplification of 9p24.1 in diffuse large b-cell lymphoma identifies a unique subset of cases that resemble primary mediastinal large b-cell lymphoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717207/ https://www.ncbi.nlm.nih.gov/pubmed/31471540 http://dx.doi.org/10.1038/s41408-019-0233-5 |
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