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Verfasst von:Schmidt, Manuel [VerfasserIn]   i
 Hochhaus, Andreas [VerfasserIn]   i
 König-Merediz, Sven A. [VerfasserIn]   i
 Brendel, Cornelia [VerfasserIn]   i
 Proba, Jutta [VerfasserIn]   i
 Hoppe, Georg J. [VerfasserIn]   i
 Wittig, Burghardt [VerfasserIn]   i
 Ehninger, Gerhard [VerfasserIn]   i
 Hehlmann, Rüdiger [VerfasserIn]   i
 Neubauer, Andreas [VerfasserIn]   i
Titel:Expression of Interferon Regulatory Factor 4 in Chronic Myeloid Leukemia
Titelzusatz:Correlation With Response to Interferon Alfa Therapy
Verf.angabe:Manuel Schmidt, Andreas Hochhaus, Sven A. König-Merediz, Cornelia Brendel, Jutta Proba, Georg J. Hoppe, Burghardt Wittig, Gerhard Ehninger, Rüdiger Hehlmann, Andreas Neubauer
Jahr:2000
Fussnoten:Gesehen am 13.04.2022
Titel Quelle:Enthalten in: Journal of clinical oncology
Ort Quelle:Alexandria, Va. : American Society of Clinical Oncology, 1983
Jahr Quelle:2000
Band/Heft Quelle:18(2000), 19, Seite 3331-3338
ISSN Quelle:1527-7755
Abstract:PURPOSE: Mice experiments have established an important role for interferon regulatory factor (IRF) family members in hematopoiesis. We wanted to study the expression of interferon regulatory factor 4 (IRF4) in various hematologic disorders, especially chronic myeloid leukemia (CML), and its association with response to interferon alfa (IFN-α) treatment in CML. - - MATERIALS AND METHODS: Blood samples from various hematopoietic cell lines, different leukemia patients (70 CML, 29 acute myeloid leukemia [AML], 10 chronic myelomonocytic leukemia [CMMoL], 10 acute lymphoblastic leukemia, and 10 chronic lymphoid leukemia patients), and 33 healthy volunteers were monitored for IRF4 expression by reverse transcriptase polymerase chain reaction. Then, with a focus on CML, the IRF4 level was determined in sorted cell subpopulations from CML patients and healthy volunteers and in in vitro-stimulated CML cells. Furthermore, IRF4 expression was compared in the CML samples taken before IFN-α therapy and in 47 additional CML samples taken during IFN-α therapy. IRF4 expression was then correlated with cytogenetic response to IFN-α. - - RESULTS: IRF4 expression was significantly impaired in CML, AML, and CMMoL samples. The downregulation of IRF4 in CML samples was predominantly found in T cells. In CML patients during IFN-α therapy, a significant increase in IRF4 levels was detected, and this was also observed in sorted T cells from CML patients. The increase seen during IFN-α therapy was not due to different blood counts. In regard to the cytogenetic response with IFN-α, a good response was associated with high IRF4 expression. - - CONCLUSION: IRF4 expression is downregulated in T cells of CML patients, and its increase is associated with a good response to IFN-α therapy. These data suggest IRF4 expression as a useful marker to monitor, if not predict, response to IFN-α in CML.
DOI:doi:10.1200/JCO.2000.18.19.3331
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 ; Verlag: https://doi.org/10.1200/JCO.2000.18.19.3331
 Volltext: https://ascopubs.org/doi/10.1200/JCO.2000.18.19.3331
 DOI: https://doi.org/10.1200/JCO.2000.18.19.3331
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1799542645
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