• Medientyp: E-Artikel
  • Titel: Automated Array-Based Genomic Profiling in Chronic Lymphocytic Leukemia: Development of a Clinical Tool and Discovery of Recurrent Genomic Alterations
  • Beteiligte: Schwaenen, Carsten; Nessling, Michelle; Wessendorf, Swen; Salvi, Tatjana; Wrobel, Gunnar; Radlwimmer, Bernhard; Kestler, Hans A.; Haslinger, Christian; Stilgenbauer, Stephan; Döhner, Hartmut; Bentz, Martin; Lichter, Peter
  • Erschienen: National Academy of Sciences, 2004
  • Erschienen in: Proceedings of the National Academy of Sciences of the United States of America, 101 (2004) 4, Seite 1039-1044
  • Sprache: Englisch
  • ISSN: 0027-8424
  • Schlagwörter: Biological Sciences
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  • Anmerkungen:
  • Beschreibung: B cell chronic lymphocytic leukemia (B-CLL) is characterized by a highly variable clinical course. Recurrent chromosomal imbalances provide significant prognostic markers. Risk-adapted therapy based on genomic alterations has become an option that is currently being tested in clinical trials. To supply a robust tool for such large scale studies, we developed a comprehensive DNA microarray dedicated to the automated analysis of recurrent genomic imbalances in B-CLL by array-based comparative genomic hybridization (matrix-CGH). Validation of this chip in a series of 106 B-CLL cases revealed a high specificity and sensitivity that fulfils the criteria for application in clinical oncology. This chip is immediately applicable within clinical B-CLL treatment trials that evaluate whether B-CLL cases with distinct chromosomal abnormalities should be treated with chemotherapy of different intensities and/or stem cell transplantation. Through the control set of DNA fragments equally distributed over the genome, recurrent genomic imbalances were discovered: trisomy of chromosome 19 and gain of the MYCN oncogene correlating with an elevation of MYCN mRNA expression.
  • Zugangsstatus: Freier Zugang