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Comprehensive analysis of PD-L1 expression in glioblastoma multiforme
Glioblastoma multiforme are highly malignant brain tumours with frequent genetic and epigenetic alterations. The poor clinical outcome of these tumours necessitates the development of new treatment options. Immunotherapies for glioblastoma multiforme including PD1/PD-L1 inhibition are currently test...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522061/ https://www.ncbi.nlm.nih.gov/pubmed/28178682 http://dx.doi.org/10.18632/oncotarget.15031 |
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author | Heiland, Dieter Henrik Haaker, Gerrit Delev, Daniel Mercas, Bianca Masalha, Waseem Heynckes, Sabrina Gäbelein, Annette Pfeifer, Dietmar Carro, Maria Stella Weyerbrock, Astrid Prinz, Marco Schnell, Oliver |
author_facet | Heiland, Dieter Henrik Haaker, Gerrit Delev, Daniel Mercas, Bianca Masalha, Waseem Heynckes, Sabrina Gäbelein, Annette Pfeifer, Dietmar Carro, Maria Stella Weyerbrock, Astrid Prinz, Marco Schnell, Oliver |
author_sort | Heiland, Dieter Henrik |
collection | PubMed |
description | Glioblastoma multiforme are highly malignant brain tumours with frequent genetic and epigenetic alterations. The poor clinical outcome of these tumours necessitates the development of new treatment options. Immunotherapies for glioblastoma multiforme including PD1/PD-L1 inhibition are currently tested in ongoing clinical trials. The purpose of this study was to investigate the molecular background of PD-L1 expression in glioblastoma multiforme and to find associated pathway activation and genetic alterations. We show that PD-L1 is up-regulated in IDH1/2 wildtype glioblastoma multiforme compared to lower-grade gliomas. In addition, a strong association of PD-L1 with the mesenchymal expression subgroup was observed. Consistent with that, NF1 mutation and corresponding activation of the MAPK pathway was strongly connected to PD-L1 expression. Our findings may explain different response to PD-L1 inhibition of patients in ongoing trials and may help to select patients that may profit of immunotherapy in the future. |
format | Online Article Text |
id | pubmed-5522061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-55220612017-08-08 Comprehensive analysis of PD-L1 expression in glioblastoma multiforme Heiland, Dieter Henrik Haaker, Gerrit Delev, Daniel Mercas, Bianca Masalha, Waseem Heynckes, Sabrina Gäbelein, Annette Pfeifer, Dietmar Carro, Maria Stella Weyerbrock, Astrid Prinz, Marco Schnell, Oliver Oncotarget Research Paper Glioblastoma multiforme are highly malignant brain tumours with frequent genetic and epigenetic alterations. The poor clinical outcome of these tumours necessitates the development of new treatment options. Immunotherapies for glioblastoma multiforme including PD1/PD-L1 inhibition are currently tested in ongoing clinical trials. The purpose of this study was to investigate the molecular background of PD-L1 expression in glioblastoma multiforme and to find associated pathway activation and genetic alterations. We show that PD-L1 is up-regulated in IDH1/2 wildtype glioblastoma multiforme compared to lower-grade gliomas. In addition, a strong association of PD-L1 with the mesenchymal expression subgroup was observed. Consistent with that, NF1 mutation and corresponding activation of the MAPK pathway was strongly connected to PD-L1 expression. Our findings may explain different response to PD-L1 inhibition of patients in ongoing trials and may help to select patients that may profit of immunotherapy in the future. Impact Journals LLC 2017-02-02 /pmc/articles/PMC5522061/ /pubmed/28178682 http://dx.doi.org/10.18632/oncotarget.15031 Text en Copyright: © 2017 Heiland et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper Heiland, Dieter Henrik Haaker, Gerrit Delev, Daniel Mercas, Bianca Masalha, Waseem Heynckes, Sabrina Gäbelein, Annette Pfeifer, Dietmar Carro, Maria Stella Weyerbrock, Astrid Prinz, Marco Schnell, Oliver Comprehensive analysis of PD-L1 expression in glioblastoma multiforme |
title | Comprehensive analysis of PD-L1 expression in glioblastoma multiforme |
title_full | Comprehensive analysis of PD-L1 expression in glioblastoma multiforme |
title_fullStr | Comprehensive analysis of PD-L1 expression in glioblastoma multiforme |
title_full_unstemmed | Comprehensive analysis of PD-L1 expression in glioblastoma multiforme |
title_short | Comprehensive analysis of PD-L1 expression in glioblastoma multiforme |
title_sort | comprehensive analysis of pd-l1 expression in glioblastoma multiforme |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522061/ https://www.ncbi.nlm.nih.gov/pubmed/28178682 http://dx.doi.org/10.18632/oncotarget.15031 |
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