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Status: Bibliographieeintrag

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Verfasst von:Blank, Anna-Eva [VerfasserIn]   i
 Baumgarten, Peter [VerfasserIn]   i
 Zeiner, Pia [VerfasserIn]   i
 Zachskorn, Cornelia [VerfasserIn]   i
 Löffler, Christian [VerfasserIn]   i
 Schittenhelm, Jens [VerfasserIn]   i
 Czupalla, Cathrin J. [VerfasserIn]   i
 Capper, David [VerfasserIn]   i
 Plate, Karl H. [VerfasserIn]   i
 Harter, Patrick N. [VerfasserIn]   i
 Mittelbronn, Michel [VerfasserIn]   i
Titel:Tumour necrosis factor receptor superfamily member 9 (TNFRSF9) is up-regulated in reactive astrocytes in human gliomas
Verf.angabe:Anna-Eva Blank, Peter Baumgarten, Pia Zeiner, Cornelia Zachskorn, Christian Löffler, Jens Schittenhelm, Cathrin J. Czupalla, David Capper, Karl H. Plate, Patrick N. Harter and Michel Mittelbronn
Jahr:2015
Jahr des Originals:2014
Umfang:12 S.
Fussnoten:Published online Article Accepted on 10 March 2014 ; Gesehen am 26.05.2020
Titel Quelle:Enthalten in: Neuropathology & applied neurobiology
Ort Quelle:Oxford [u.a.] : Wiley-Blackwell, 1975
Jahr Quelle:2015
Band/Heft Quelle:41(2015), 2, Seite e56-e67
ISSN Quelle:1365-2990
Abstract:Aims The prognosis of patients with malignant gliomas is still dismal despite maximum treatment. Novel therapeutic alternatives targeting tumorigenic pathways are, therefore, demanded. In murine glioma models, targeting of tumour necrosis factor receptor superfamily (TNFRSF) 9 led to complete tumour eradication. Thus, TNFRSF9 might also constitute a promising target in human diffuse gliomas. As there is a lack of data, we aimed to define the expression pattern and cellular source of TNFRSF9 in human gliomas. Methods We investigated TNFRSF9 expression in normal human central nervous system (CNS) tissue and glioma specimens using immunohistochemistry, immunofluorescence and Western blotting techniques. Results Our results show that TNFRSF9 is considerably up-regulated in human gliomas when compared with normal brain tissue. In addition, our data provides evidence for an immune cell-independent de novo expression pattern of TNFRSF9 in mainly non-neoplastic reactive astrocytes and excludes classic immunological cell types, namely lymphocytes and microglia as the source of TNFRSF9. Moreover, TNFRSF9 is predominantly expressed in a perivascular and peritumoural distribution with significantly higher expression in IDH-1 mutant gliomas. Conclusions Our findings provide a novel, TNFRSF9-positive, reactive astrocytic phenotype and challenge the therapeutic suitability of TNFRSF9 as a promising target for human gliomas.
DOI:doi:10.1111/nan.12135
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1111/nan.12135
 Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1111/nan.12135
 DOI: https://doi.org/10.1111/nan.12135
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:astrocytes
 CD137
 glioma
 gliosis
 TNFRSF9
K10plus-PPN:1698825048
Verknüpfungen:→ Zeitschrift

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