Expression of nuclear transcription factor interferon consensus sequence binding protein in chronic myeloid leukemia correlates with pretreatment risk features and cytogenetic response to interferon-α

Recently, it was shown that interferon consensus sequence binding protein (ICSBP), a member of the interferon regulatory factor (IRF) family, has a potential role in chronic myeloid leukemia (CML). Deletion of ICSBP gene in mice leads to a CML-like syndrome and samples from CML patients exhibited im...

Full description

Saved in:
Bibliographic Details
Main Authors: Schmidt, Manuel (Author) , Hochhaus, Andreas (Author) , Nitsche, Andreas (Author) , Hehlmann, Rüdiger (Author) , Neubauer, Andreas (Author)
Format: Article (Journal)
Language:English
Published: June 1, 2001
In: Blood
Year: 2001, Volume: 97, Issue: 11, Pages: 3648-3650
ISSN:1528-0020
DOI:10.1182/blood.V97.11.3648
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1182/blood.V97.11.3648
Get full text
Author Notes:Manuel Schmidt, Andreas Hochhaus, Andreas Nitsche, Rüdiger Hehlmann, and Andreas Neubauer
Description
Summary:Recently, it was shown that interferon consensus sequence binding protein (ICSBP), a member of the interferon regulatory factor (IRF) family, has a potential role in chronic myeloid leukemia (CML). Deletion of ICSBP gene in mice leads to a CML-like syndrome and samples from CML patients exhibited impaired ICSBP expression. The present study found that ICSBP expression correlated with risk features determined by Sokal score in untreated CML (P = .007 for high versus low risk). In addition, analyzing ICSBP expression during interferon-α (IFN-α) therapy in “good” (n = 27) versus “poor” (n = 15) cytogenetic responders, high ICSBP levels were only observed in “good” responders (P = .0002). Together, these data suggest that ICSBP levels are related to initial presentation of CML and the therapeutic response of CML to IFN-α, indicating an important role of ICSBP in CML.
Item Description:Gesehen am 18.05.2022
Physical Description:Online Resource
ISSN:1528-0020
DOI:10.1182/blood.V97.11.3648