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Verfasst von:Reuter, Tasmin [VerfasserIn]   i
 Warta, Rolf [VerfasserIn]   i
 Theile, Dirk [VerfasserIn]   i
 Meid, Andreas [VerfasserIn]   i
 Rigalli, Juan Pablo [VerfasserIn]   i
 Mogler, Carolin [VerfasserIn]   i
 Herpel, Esther [VerfasserIn]   i
 Grabe, Niels [VerfasserIn]   i
 Lahrmann, Bernd [VerfasserIn]   i
 Plinkert, Peter K. [VerfasserIn]   i
 Herold-Mende, Christel [VerfasserIn]   i
 Dyckhoff, Gerhard [VerfasserIn]   i
 Haefeli, Walter E. [VerfasserIn]   i
 Weiß, Johanna [VerfasserIn]   i
Titel:Role of NR1I2 (pregnane X receptor) polymorphisms in head and neck squamous cell carcinoma
Verf.angabe:Tasmin Reuter, Rolf Warta, Dirk Theile, Andreas D. Meid, Juan Pablo Rigalli, Carolin Mogler, Esther Herpel, Niels Grabe, Bernd Lahrmann, Peter K. Plinkert, Christel Herold-Mende, Gerhard Dyckhoff, Walter Emil Haefeli, Johanna Weiss
E-Jahr:2015
Jahr:4 July 2015
Umfang:10 S.
Fussnoten:Gesehen am 18.06.2020
Titel Quelle:Enthalten in: Naunyn-Schmiedeberg's archives of pharmacology
Ort Quelle:Berlin : Springer, 1873
Jahr Quelle:2015
Band/Heft Quelle:388(2015), 11, Seite 1141-1150
ISSN Quelle:1432-1912
Abstract:The pregnane X receptor (PXR) is a transcription factor regulating genes involved not only in pharmacokinetics but also in chemotherapy resistance and cancer progression. The significance of PXR for survival of head and neck squamous cell carcinoma (HNSCC) patients is unknown so far. Single nucleotide polymorphisms (SNPs) in the PXR-encoding NR1I2 gene influence receptor functionality and inducibility by ligands and thus modulate expression and activity of its target genes. In this study, seven SNPs in the NR1I2 gene were investigated for an association with PXR protein expression and survival of HNSCC patients. Genotyping was conducted using hybridisation probe format methodology. PXR protein expression was quantified by immunohistochemistry of tissue microarray samples of HNSCC biopsies. Genotypes were correlated to PXR protein expression by a linear model regressing on the continuous gene expression value and a Cox model regressing on overall survival times. Haplotype analysis was performed by reconstruction of haplotypes from genotype information according to the expectation-maximisation algorithm. Of all tested SNPs, rs1054190 and rs1054191 allele variants tended to correlate with a reduced protein expression score of PXR (p = 0.088). Four haplotypes, each consisting of two SNPs, rs3814055/rs1054190 and rs3814055/rs1054191 as well as rs1523127/rs1054190 and rs1523127/rs1054191, showed a significant reduction of the PXR expression score (p = 0.049 and p = 0.032). However, neither allele variants nor haplotypes influenced overall survival of the respective patients. Certain NR1I2 SNPs showed an impact on PXR protein expression in HNSCC but did not influence overall survival times, questioning their value as prognostic biomarkers.
DOI:doi:10.1007/s00210-015-1150-1
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/10.1007/s00210-015-1150-1
 DOI: https://doi.org/10.1007/s00210-015-1150-1
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1701022540
Verknüpfungen:→ Zeitschrift

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