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Integrated analysis of programmed cell death ligand 1 expression reveals increased levels in high-grade glioma
PURPOSE: Gliomas are the most frequent primary brain tumors of adults. Despite intensive research, there are still no targeted therapies available. Here, we performed an integrated analysis of glioma and programmed cell death ligand 1 (PD-L1) in 90 samples including 58 glioma and 32 control brain ti...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236471/ https://www.ncbi.nlm.nih.gov/pubmed/33963441 http://dx.doi.org/10.1007/s00432-021-03656-w |
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author | Hölzl, Dorothee Hutarew, Georg Zellinger, Barbara Schlicker, Hans U. Schwartz, Christoph Winkler, Peter A. Sotlar, Karl Kraus, Theo F. J. |
author_facet | Hölzl, Dorothee Hutarew, Georg Zellinger, Barbara Schlicker, Hans U. Schwartz, Christoph Winkler, Peter A. Sotlar, Karl Kraus, Theo F. J. |
author_sort | Hölzl, Dorothee |
collection | PubMed |
description | PURPOSE: Gliomas are the most frequent primary brain tumors of adults. Despite intensive research, there are still no targeted therapies available. Here, we performed an integrated analysis of glioma and programmed cell death ligand 1 (PD-L1) in 90 samples including 58 glioma and 32 control brain tissues. METHODS: To identify PD-L1 expression in glioma, we performed immunohistochemical analysis of PD-L1 tumor proportion score (TPS) using the clinically valid PD-L1 22C3 antibody on 90 samples including controls and WHO grade I–IV gliomas. RESULTS: We found that PD-L1 is highly expressed in a subfraction of glioma cells. Analysis of PD-L1 levels in different glioma subtypes revealed a strong intertumoral variation of PD-L1 protein. Furthermore, we correlated PD-L1 expression with molecular glioma hallmarks such as MGMT-promoter methylation, IDH1/2 mutations, TERT promoter mutations and LOH1p/19q. CONCLUSION: In summary, we found that PD-L1 is highly expressed in a subfraction of glioma, indicating PD-L1 as a potential new marker in glioma assessment opening up novel therapeutic approaches. |
format | Online Article Text |
id | pubmed-8236471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-82364712021-07-09 Integrated analysis of programmed cell death ligand 1 expression reveals increased levels in high-grade glioma Hölzl, Dorothee Hutarew, Georg Zellinger, Barbara Schlicker, Hans U. Schwartz, Christoph Winkler, Peter A. Sotlar, Karl Kraus, Theo F. J. J Cancer Res Clin Oncol Original Article – Cancer Research PURPOSE: Gliomas are the most frequent primary brain tumors of adults. Despite intensive research, there are still no targeted therapies available. Here, we performed an integrated analysis of glioma and programmed cell death ligand 1 (PD-L1) in 90 samples including 58 glioma and 32 control brain tissues. METHODS: To identify PD-L1 expression in glioma, we performed immunohistochemical analysis of PD-L1 tumor proportion score (TPS) using the clinically valid PD-L1 22C3 antibody on 90 samples including controls and WHO grade I–IV gliomas. RESULTS: We found that PD-L1 is highly expressed in a subfraction of glioma cells. Analysis of PD-L1 levels in different glioma subtypes revealed a strong intertumoral variation of PD-L1 protein. Furthermore, we correlated PD-L1 expression with molecular glioma hallmarks such as MGMT-promoter methylation, IDH1/2 mutations, TERT promoter mutations and LOH1p/19q. CONCLUSION: In summary, we found that PD-L1 is highly expressed in a subfraction of glioma, indicating PD-L1 as a potential new marker in glioma assessment opening up novel therapeutic approaches. Springer Berlin Heidelberg 2021-05-08 2021 /pmc/articles/PMC8236471/ /pubmed/33963441 http://dx.doi.org/10.1007/s00432-021-03656-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article – Cancer Research Hölzl, Dorothee Hutarew, Georg Zellinger, Barbara Schlicker, Hans U. Schwartz, Christoph Winkler, Peter A. Sotlar, Karl Kraus, Theo F. J. Integrated analysis of programmed cell death ligand 1 expression reveals increased levels in high-grade glioma |
title | Integrated analysis of programmed cell death ligand 1 expression reveals increased levels in high-grade glioma |
title_full | Integrated analysis of programmed cell death ligand 1 expression reveals increased levels in high-grade glioma |
title_fullStr | Integrated analysis of programmed cell death ligand 1 expression reveals increased levels in high-grade glioma |
title_full_unstemmed | Integrated analysis of programmed cell death ligand 1 expression reveals increased levels in high-grade glioma |
title_short | Integrated analysis of programmed cell death ligand 1 expression reveals increased levels in high-grade glioma |
title_sort | integrated analysis of programmed cell death ligand 1 expression reveals increased levels in high-grade glioma |
topic | Original Article – Cancer Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236471/ https://www.ncbi.nlm.nih.gov/pubmed/33963441 http://dx.doi.org/10.1007/s00432-021-03656-w |
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