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Projekt Druckansicht

Rolle von Cks1 für l-abhängige und -unabhängige Zellzyklusregulation, Überleben und Quieszenz in normaler und leukämischer Hämatopoese

Fachliche Zuordnung Hämatologie, Onkologie
Förderung Förderung von 2012 bis 2015
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 223306220
 
Erstellungsjahr 2016

Zusammenfassung der Projektergebnisse

We identified Cks1 as an essential regulator of HSC fate operating upstream of the CKI p27, p21 and p57, and the Rb family member p130. Cks1 loss prominently affects the most immature CD150+ LSK HSC compartment by inhibiting exit from quiescence and cell cycling, and protects more mature HPC from apoptosis. Our analyses revealed that p27 is an essential downstream target of the SCFSkp2-Cks1 complex in the regulation of early hematopoiesis. Most likely all SCFSkp2/Cks1 CKI targets and p130 are involved in the HSC/HPC control. Only genetic in vivo studies involving composite gene kockout mice would allow deciphering this complex network. In CML, Cks1 is overexpressed. Cks1 is a mediator of Bcr-Ablinduced clonogenic activity, where Bcr-Abl expression also involves high Myc levels. Therefore Cks1 is proposed to be a central intermediate for normal and oncogene-induced hematopoietic cell cycle regulation. Cks1 thus represents a therapeutic target in various hematologic malignancies.

Projektbezogene Publikationen (Auswahl)

  • (2014) Disruption of the PRKCD-FBXO25-HAX-1 axis attenuates the apoptotic response and drives lymphomagenesis, Nature medicine 20, 1401-1409
    Baumann, U., Fernandez-Saiz, V., Rudelius, M., Lemeer, S., Rad, R., Knorn, A. M., Slawska, J., Engel, K., Jeremias, I., Li, Z., Tomiatti, V., Illert, A. L., Targosz, B. S., Braun, M., Perner, S., Leitges, M., Klapper, W., Dreyling, M., Miething, C., Lenz, G., Rosenwald, A., Peschel, C., Keller, U., Kuster, B., and Bassermann, F.
    (Siehe online unter https://doi.org/10.1038/nm.3740)
  • (2014) Mycinduced SUMOylation is a therapeutic vulnerability for B-cell lymphoma, Blood 124, 2081-2090
    Hoellein, A., Fallahi, M., Schoeffmann, S., Steidle, S., Schaub, F. X., Rudelius, M., Laitinen, I., Nilsson, L., Goga, A., Peschel, C., Nilsson, J. A., Cleveland, J. L., and Keller, U.
    (Siehe online unter https://doi.org/10.1182/blood-2014-06-584524)
  • (2015) Cks1 is a critical regulator of hematopoietic stem cell quiescence and cycling, operating upstream of Cdk inhibitors, Oncogene 34, 4347-4357
    Tomiatti, V., Istvanffy, R., Pietschmann, E., Kratzat, S., Hoellein, A., Quintanilla-Fend, L., von Bubnoff, N., Peschel, C., Oostendorp, R. A., and Keller, U.
    (Siehe online unter https://doi.org/10.1038/onc.2014.364)
  • (2015) Disclosing the CXCR4 Expression in Lymphoproliferative Diseases by Targeted Molecular Imaging, Theranostics 5, 618-630
    Wester, H. J., Keller, U., Schottelius, M., Beer, A., Philipp-Abbrederis, K., Hoffmann, F., Simecek, J., Gerngross, C., Lassmann, M., Herrmann, K., Pellegata, N., Rudelius, M., Kessler, H., and Schwaiger, M.
    (Siehe online unter https://doi.org/10.7150/thno.11251)
  • (2015) In vivo hematopoietic Myc activation directs a transcriptional signature in endothelial cells within the bone marrow microenvironment, Oncotarget 6, 21827-39
    Franke, K., Vilne, B., Da Costa, O., Rudelius, M., Peschel, C., Oostendorp, R. A., and Keller, U.
    (Siehe online unter https://doi.org/10.18632/oncotarget.5217)
  • (2015) In vivo molecular imaging of chemokine receptor CXCR4 expression in patients with advanced multiple myeloma, EMBO molecular medicine 7, 477-487
    Philipp-Abbrederis, K., Herrmann, K., Knop, S., Schottelius, M., Eiber, M., Luckerath, K., Pietschmann, E., Habringer, S., Gerngross, C., Franke, K., Rudelius, M., Schirbel, A., Lapa, C., Schwamborn, K., Steidle, S., Hartmann, E., Rosenwald, A., Kropf, S., Beer, A. J., Peschel, C., Einsele, H., Buck, A. K., Schwaiger, M., Gotze, K., Wester, H. J., and Keller, U.
    (Siehe online unter https://doi.org/10.15252/emmm.201404698)
 
 

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