The activation of intracellular tyrosine kinases by interferon-alpha (IFNα) correlates with its antiproliferative activity in B-lymphoid cell lines, but not in B-cell chronic lymphocytic leukemia patients

التفاصيل البيبلوغرافية
العنوان: The activation of intracellular tyrosine kinases by interferon-alpha (IFNα) correlates with its antiproliferative activity in B-lymphoid cell lines, but not in B-cell chronic lymphocytic leukemia patients
المؤلفون: T. Kamp, Bertold Emmerich, S. Adler, Susanne Danhauser-Riedl, Michael Hallek, Christoph Nerl, N von Bubnoff
المصدر: Scopus-Elsevier
بيانات النشر: Springer Science and Business Media LLC, 2000.
سنة النشر: 2000
مصطلحات موضوعية: Male, Chronic lymphocytic leukemia, medicine.medical_treatment, Biology, Cell Line, chemistry.chemical_compound, Cytosol, hemic and lymphatic diseases, Tumor Cells, Cultured, medicine, Humans, Phosphorylation, Tyrosine, Aged, B-Lymphocytes, Cell growth, Interferon-alpha, Proteins, Tyrosine phosphorylation, Hematology, General Medicine, Middle Aged, Protein-Tyrosine Kinases, medicine.disease, Leukemia, Lymphocytic, Chronic, B-Cell, Enzyme Activation, Cytokine, chemistry, Cell culture, Cancer research, Female, Extracellular Space, Tyrosine kinase, Cell Division
الوصف: The response to interferon-alpha (IFNalpha) treatment in leukemias of the B-cell lineage shows a marked heterogeneity. A distinct subset of patients with B-CLL responds to treatment with IFNalpha, while the drug has no therapeutic effect in the majority of patients. The mechanism of this phenomenon is poorly understood. The cellular events induced by this cytokine mediated by a number of specific signaling events. Therefore, we studied the effect of recombinant IFNalpha on tyrosine phosphorylation and proliferation of cytosolic proteins in human cell lines and in freshly isolated B-CLL cells in order to test the potential value of these events as a pretreatment test for IFNalpha in CLL. In human lymphoid cell lines, IFNalpha induced tyrosine phosphorylation of multiple cytosolic proteins in a time- and concentration-dependent manner. This effect correlated with its growth-inhibitory effect in almost all cell lines. In marked contrast, in freshly isolated B-CLL cells IFNalpha seemed to have both stimulatory and inhibitory effects on proliferation, but it consistently stimulated tyrosine phosphorylation. Moreover, the clinical response of B-CLL to IFNalpha did not correlate with the activation of tyrosine kinases nor with the inhibition of cell growth in vitro. Therefore, the assessment of IFNalpha-induced tyrosine phosphorylation of cytosolic phospho-proteins does not allow to predict the treatment response to IFNalpha in CLL patients.
تدمد: 1432-0584
0939-5555
DOI: 10.1007/s002770050566
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34ff250765da2884e5aee4ec485ff030
https://doi.org/10.1007/s002770050566
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....34ff250765da2884e5aee4ec485ff030
قاعدة البيانات: OpenAIRE
الوصف
تدمد:14320584
09395555
DOI:10.1007/s002770050566