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Status: Bibliographieeintrag

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Verfasst von:Linnebacher, Alica [VerfasserIn]   i
 Mayer, Philipp [VerfasserIn]   i
 Marnet, Nicole [VerfasserIn]   i
 Bergmann, Frank [VerfasserIn]   i
 Herpel, Esther [VerfasserIn]   i
 Revia, Steffie [VerfasserIn]   i
 Yin, Libo [VerfasserIn]   i
 Liu, Li [VerfasserIn]   i
 Hackert, Thilo [VerfasserIn]   i
 Giese, Thomas [VerfasserIn]   i
 Herr, Ingrid [VerfasserIn]   i
 Gaida, Matthias [VerfasserIn]   i
Titel:Interleukin 21 receptor/ligand interaction is linked to disease progression in pancreatic cancer
Verf.angabe:Alica Linnebacher, Philipp Mayer, Nicole Marnet, Frank Bergmann, Esther Herpel, Steffie Revia, Libo Yin, Li Liu, Thilo Hackert, Thomas Giese, Ingrid Herr and Matthias M. Gaida
E-Jahr:2019
Jahr:18 September 2019
Umfang:18 S.
Fussnoten:Gesehen am 31.10.2019
Titel Quelle:Enthalten in: Cells
Ort Quelle:Basel : MDPI, 2012
Jahr Quelle:2019
Band/Heft Quelle:8(2019), 9, Artikel-ID 1104, Seite 1-18
ISSN Quelle:2073-4409
Abstract:Pancreatic ductal adenocarcinoma (PDAC) displays a marked fibro-inflammatory microenvironment in which infiltrated immune cells fail to eliminate the tumor cells and often—rather paradoxically—promote tumor progression. Of special interest are tumor-promoting T cells that assume a Th17-like phenotype because their presence in PDAC tissue is associated with a poor prognosis. In that context, the role of IL-21, a major cytokine released by Th17-like cells, was assessed. In all tissue samples (n = 264) IL-21+ immune cells were detected by immunohistochemistry and high density of those cells was associated with poor prognosis. In the majority of patients (221/264), tumor cells expressed the receptor for IL-21 (IL-21R) and also a downstream target of IL-21, Blimp-1 (199/264). Blimp-1 expression closely correlated with IL-21R expression and multivariate analysis revealed that expression of both IL-21R and Blimp-1 was associated with shorter survival time of the patients. In vitro data using pancreatic tumor cells lines provided a possible explanation: IL-21 activated ERK and STAT3 pathways and upregulated Blimp-1. Moreover, IL-21 increased invasion of tumor cell lines in a Blimp-1-dependent manner. As an in vivo correlate, an avian xenograft model was used. Here again Blimp-1 expression was significantly upregulated in IL-21 stimulated tumor cells. In summary, our data showed an association of IL-21+ immune cell infiltration and IL-21 receptor expression in PDAC with poor survival, most likely due to an IL-21-mediated promotion of tumor cell invasion and enhanced colony formation, supporting the notion of the tumor-promoting abilities of the tumor microenvironment.
DOI:doi:10.3390/cells8091104
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: https://doi.org/10.3390/cells8091104
 Verlag: https://www.mdpi.com/2073-4409/8/9/1104
 DOI: https://doi.org/10.3390/cells8091104
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Blimp-1
 IL-21
 invasion
 pancreatic cancer
 Th17
 tumor microenvironment
K10plus-PPN:1680821555
Verknüpfungen:→ Zeitschrift

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