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Published in: Journal of Cancer Research and Clinical Oncology 8/2021

Open Access 01-08-2021 | Glioblastoma | Original Article – Cancer Research

Integrated analysis of programmed cell death ligand 1 expression reveals increased levels in high-grade glioma

Authors: Dorothee Hölzl, Georg Hutarew, Barbara Zellinger, Hans U. Schlicker, Christoph Schwartz, Peter A. Winkler, Karl Sotlar, Theo F. J. Kraus

Published in: Journal of Cancer Research and Clinical Oncology | Issue 8/2021

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Abstract

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.
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Metadata
Title
Integrated analysis of programmed cell death ligand 1 expression reveals increased levels in high-grade glioma
Authors
Dorothee Hölzl
Georg Hutarew
Barbara Zellinger
Hans U. Schlicker
Christoph Schwartz
Peter A. Winkler
Karl Sotlar
Theo F. J. Kraus
Publication date
01-08-2021
Publisher
Springer Berlin Heidelberg
Published in
Journal of Cancer Research and Clinical Oncology / Issue 8/2021
Print ISSN: 0171-5216
Electronic ISSN: 1432-1335
DOI
https://doi.org/10.1007/s00432-021-03656-w

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