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ZAP-70 expression is a prognostic factor in chronic lymphocytic leukemia.
Dürig, J; Nückel, H; Cremer, M; Führer, A; Halfmeyer, K; Fandrey, J; Möröy, T; Klein-Hitpass, L; Dührsen, U.
Afiliação
  • Dürig J; Department of Hematology, University Hospital Essen, University of Duisburg-Essen, Germany.
Leukemia ; 17(12): 2426-34, 2003 Dec.
Article em En | MEDLINE | ID: mdl-14523469
B-cell chronic lymphocytic leukemia (B-CLL) is a heterogenous disease with a highly variable clinical course. Recent studies have shown that expression of the protein tyrosine kinase ZAP-70 may serve as a prognostic marker in B-CLL. Employing a semiquantitative RT-PCR assay, we examined purified leukemia B cells of 39 CLL patients for the expression of ZAP-70 mRNA transcripts. Significant ZAP-70 mRNA levels exceeding those found in control samples with 5% T cells were detected in 36% of the CLL cases. Patients in the ZAP-70 positive cohort were characterized by an unfavorable clinical course with a significantly shorter progression-free survival as compared to the ZAP-70-negative patients (64%). These results were confirmed by flow-cytometric analysis of the ZAP-70 protein, and expanded to a larger patient cohort (n=67). A combined statistical analysis of 79 patients showed that the two patient subgroups also differed with regard to overall survival and a panel of known clinical prognostic factors including LDH, thymidine kinase serum levels and expression of the CD38 surface antigen by the leukemic cell clone. The level of ZAP-70 expression did not change over time in the majority of patients where sequential samples were available for analysis.
Assuntos
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Base de dados: MEDLINE Assunto principal: Proteínas Tirosina Quinases / Leucemia Linfocítica Crônica de Células B / Biomarcadores Tumorais Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2003 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Proteínas Tirosina Quinases / Leucemia Linfocítica Crônica de Células B / Biomarcadores Tumorais Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2003 Tipo de documento: Article