Navigation überspringen
Universitätsbibliothek Heidelberg
Status: Bibliographieeintrag

Verfügbarkeit
Standort: ---
Exemplare: ---
heiBIB
 Online-Ressource
Verfasst von:Rahn, Kerstin [VerfasserIn]   i
 Abdallah, Ali T. [VerfasserIn]   i
 Gan, Lin [VerfasserIn]   i
 Herbrich, Shelley [VerfasserIn]   i
 Sonntag, Roland [VerfasserIn]   i
 Benitez, Oscar [VerfasserIn]   i
 Malaney, Prerna [VerfasserIn]   i
 Zhang, Xiaorui [VerfasserIn]   i
 Rodriguez, Ashely G. [VerfasserIn]   i
 Brottem, Jared [VerfasserIn]   i
 Marx, Gernot [VerfasserIn]   i
 Bruemmendorf, Tim H. [VerfasserIn]   i
 Ostareck, Dirk H. [VerfasserIn]   i
 Ostareck-Lederer, Antje [VerfasserIn]   i
 Crysandt, Martina [VerfasserIn]   i
 Post, Sean M. [VerfasserIn]   i
 Naarmann-de Vries, Isabel S. [VerfasserIn]   i
Titel:Insight into the mechanism of AML del(9q) progression
Titelzusatz:hnRNP K targets the myeloid master regulators CEBPA (C/EBPα) and SPI1 (PU.1)
Verf.angabe:Kerstin Rahn, Ali T. Abdallah, Lin Gan, Shelley Herbrich, Roland Sonntag, Oscar Benitez, Prerna Malaney, Xiaorui Zhang, Ashely G. Rodriguez, Jared Brottem, Gernot Marx, Tim H. Bruemmendorf, Dirk H. Ostareck, Antje Ostareck-Lederer, Martina Crysandt, Sean M. Post, Isabel S. Naarmann-de Vries
E-Jahr:2024
Jahr:March 2024
Umfang:13 S.
Fussnoten:Gesehen am 27.11.2024
Titel Quelle:Enthalten in: Biochimica et biophysica acta. Gene regulatory mechanisms
Ort Quelle:Amsterdam [u.a.] : Elsevier, 2008
Jahr Quelle:2024
Band/Heft Quelle:1867(2024), 1 vom: März, Artikel-ID 195004, Seite 1-13
ISSN Quelle:1876-4320
Abstract:Deletions on the long arm of chromosome 9 (del(9q)) are recurrent abnormalities in about 2 % of acute myeloid leukemia cases, which usually involve HNRNPK and are frequently associated with other known aberrations. Based on an Hnrnpk haploinsufficient mouse model, a recent study demonstrated a function of hnRNP K in pathogenesis of myeloid malignancies via the regulation of cellular proliferation and myeloid differentiation programs. Here, we provide evidence that reduced hnRNP K expression results in the dysregulated expression of C/EBP alpha and additional transcription factors. CyTOF analysis revealed monocytic skewing with increased levels of mature myeloid cells. To explore the role of hnRNP K during normal and pathological myeloid differentiation in humans, we characterized hnRNP K-interacting RNAs in human AML cell lines. Notably, RNA-sequencing revealed several mRNAs encoding key transcription factors involved in the regulation of myeloid differentiation as targets of hnRNP K. We showed that specific sequence motifs confer the interaction of SPI1 and CEBPA 5 ' and 3 ' UTRs with hnRNP K. The siRNA mediated reduction of hnRNP K in human AML cells resulted in an increase of PU.1 and C/EBP alpha that is most pronounced for the p30 isoform. The combinatorial treatment with the inducer of myeloid differentiation valproic acid resulted in increased C/EBP alpha expression and myeloid differentiation. Together, our results indicate that hnRNP K post-transcriptionally regulates the expression of myeloid master transcription factors. These novel findings can inaugurate novel options for targeted treatment of AML del (9q) by modulation of hnRNP K function.
DOI:doi:10.1016/j.bbagrm.2023.195004
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.bbagrm.2023.195004
 Volltext: https://www.sciencedirect.com/science/article/pii/S1874939923000998?via%3Dihub
 DOI: https://doi.org/10.1016/j.bbagrm.2023.195004
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:ACUTE MYELOGENOUS LEUKEMIA
 AML
 C-JUN EXPRESSION
 CEBPA
 del(9q)
 DIFFERENTIATION
 DNA-BINDING
 GENE-EXPRESSION
 HNRNPK
 MESSENGER-RNA
 NUCLEAR-RIBONUCLEOPROTEIN-K
 PROTEIN
 SPI1
 TRANSCRIPTION FACTOR
 TUMOR-SUPPRESSOR
K10plus-PPN:1909626945
Verknüpfungen:→ Zeitschrift

Permanenter Link auf diesen Titel (bookmarkfähig):  https://katalog.ub.uni-heidelberg.de/titel/69277295   QR-Code
zum Seitenanfang