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Status: Bibliographieeintrag

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Verfasst von:Valdora, Francesca [VerfasserIn]   i
 Banelli, Barbara [VerfasserIn]   i
 Stigliani, Sara [VerfasserIn]   i
 Pfister, Stefan [VerfasserIn]   i
 Moretti, Stefano [VerfasserIn]   i
 Kool, Marcel [VerfasserIn]   i
 Remke, Marc [VerfasserIn]   i
 Bai, Alfa H. C. [VerfasserIn]   i
 Brigati, Claudio [VerfasserIn]   i
 Hielscher, Thomas [VerfasserIn]   i
 Romani, Massimo [VerfasserIn]   i
 Servidei, Tiziana [VerfasserIn]   i
 Zollo, Massimo [VerfasserIn]   i
 Cinalli, Giuseppe [VerfasserIn]   i
 Oberthür, Carl André [VerfasserIn]   i
 Tonini, Gian Paolo [VerfasserIn]   i
 Coco, Simona [VerfasserIn]   i
Titel:Epigenetic silencing of DKK3 in medulloblastoma
Verf.angabe:Francesca Valdora, Barbara Banelli, Sara Stigliani, Stefan M. Pfister, Stefano Moretti, Marcel Kool, Marc Remke, Alfa H.C. Bai, Claudio Brigati, Thomas Hielscher, Massimo Romani, Tiziana Servidei, Massimo Zollo, Giuseppe Cinalli, André Oberthuer, Gian Paolo Tonini and Simona Coco
E-Jahr:2013
Jahr:8 April 2013
Umfang:14 S.
Fussnoten:Gesehen am 21.02.2022
Titel Quelle:Enthalten in: International journal of molecular sciences
Ort Quelle:Basel : Molecular Diversity Preservation International, 2000
Jahr Quelle:2013
Band/Heft Quelle:14(2013), 4, Seite 7492-7505
ISSN Quelle:1422-0067
 1661-6596
Abstract:Medulloblastoma (MB) is a malignant pediatric brain tumor arising in the cerebellum consisting of four distinct subgroups: WNT, SHH, Group 3 and Group 4, which exhibit different molecular phenotypes. We studied the expression of Dickkopf (DKK) 1-4 family genes, inhibitors of the Wnt signaling cascade, in MB by screening 355 expression profiles derived from four independent datasets. Upregulation of DKK1, DKK2 and DKK4 mRNA was observed in the WNT subgroup, whereas DKK3 was downregulated in 80% MBs across subgroups with respect to the normal cerebellum (p < 0.001). Since copy number aberrations targeting the DKK3 locus (11p15.3) are rare events, we hypothesized that epigenetic factors could play a role in DKK3 regulation. Accordingly, we studied 77 miRNAs predicting to repress DKK3; however, no significant inverse correlation between miRNA/mRNA expression was observed. Moreover, the low methylation levels in the DKK3 promoters (median: 3%, 5% and 5% for promoter 1, 2 and 3, respectively) excluded the downregulation of gene expression by methylation. On the other hand, the treatment of MB cells with Trichostatin A (TSA), a potent inhibitor of histone deacetylases (HDAC), was able to restore both DKK3 mRNA and protein. In conclusion, DKK3 downregulation across all MB subgroups may be due to epigenetic mechanisms, in particular, through chromatin condensation.
DOI:doi:10.3390/ijms14047492
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/ijms14047492
 Volltext: https://www.mdpi.com/1422-0067/14/4/7492
 DOI: https://doi.org/10.3390/ijms14047492
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:DKK family
 DKK3 downregulation
 histone deacetylase
 medulloblastoma
 TSA
 Wnt antagonists
K10plus-PPN:1793375267
Verknüpfungen:→ Zeitschrift

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