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Status: Bibliographieeintrag

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Verfasst von:Merz, Constanze [VerfasserIn]   i
 von Mässenhausen, Anne [VerfasserIn]   i
 Queisser, Angela [VerfasserIn]   i
 Vogel, Wenzel [VerfasserIn]   i
 Andrén, Ove [VerfasserIn]   i
 Kirfel, Jutta [VerfasserIn]   i
 Duensing, Stefan [VerfasserIn]   i
 Perner, Sven [VerfasserIn]   i
 Nowak, Michael [VerfasserIn]   i
Titel:IL-6 overexpression in ERG-Positive prostate cancer is mediated by prostaglandin receptor EP2
Verf.angabe:Constanze Merz, Anne von Mässenhausen, Angela Queisser, Wenzel Vogel, Ove Andrén, Jutta Kirfel, Stefan Duensing, Sven Perner, and Michael Nowak
E-Jahr:2016
Jahr:April 2016
Umfang:11 S.
Fussnoten:Gesehen am 04.05.2020
Titel Quelle:Enthalten in: The American journal of pathology
Ort Quelle:New York [u.a.] : Elsevier, 1925
Jahr Quelle:2016
Band/Heft Quelle:186(2016), 4, Seite 974-984
ISSN Quelle:1525-2191
Abstract:Prostate cancer is the most diagnosed cancer in men and multiple risk factors and genetic alterations have been described. The TMPRSS2-ERG fusion event and the overexpression of the transcription factor ERG are present in approximately 50% of all prostate cancer patients, however, the clinical outcome is still controversial. Prostate tumors produce various soluble factors, including the pleiotropic cytokine IL-6, regulating cellular processes such as proliferation and metastatic segregation. Here, we used prostatectomy samples in a tissue microarray format and analyzed the co-expression and the clinicopathologic data of ERG and IL-6 using immunohistochemical double staining and correlated the read-out with clinicopathologic data. Expression of ERG and IL-6 correlated strongly in prostate tissue samples. Forced expression of ERG in prostate tumor cell lines resulted in significantly increased secretion of IL-6, whereas the down-regulation of ERG decreased IL-6 secretion. By dissecting the underlying mechanism in prostate tumor cell lines we show the ERG-mediated up-regulation of the prostanoid receptors EP2 and EP3. The prostanoid receptor EP2 was overexpressed in human prostate cancer tissue. Furthermore, the proliferation rate and IL-6 secretion in DU145 cells was reduced after treatment with EP2-receptor antagonist. Collectively, our study shows that the expression of ERG in prostate cancer is linked to the expression of IL-6 mediated by the prostanoid receptor EP2.
DOI:doi:10.1016/j.ajpath.2015.12.009
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/10.1016/j.ajpath.2015.12.009
 DOI: https://doi.org/10.1016/j.ajpath.2015.12.009
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Aged
 Biomarkers, Tumor
 Cell Line, Tumor
 Disease-Free Survival
 Down-Regulation
 Gene Expression Regulation, Neoplastic
 Humans
 Interleukin-6
 Male
 Middle Aged
 Prostate
 Prostatectomy
 Prostatic Neoplasms
 Receptors, Prostaglandin E, EP2 Subtype
 Up-Regulation
K10plus-PPN:1697017703
Verknüpfungen:→ Zeitschrift

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