High resolution copy number analysis of IRF4 translocation-positive diffuse large B-cell and follicular lymphomas
Translocations affecting chromosome subband 6p25.3 containing the IRF4 gene have been recently described as characteristic alterations in a molecularly distinct subset of germinal center B-cell-derived lymphomas. Secondary changes have yet only been described in few of these lymphomas. Here, we perf...
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| Main Authors: | , , , , , , , , , , , , , , , , , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
2013
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| In: |
Genes, chromosomes & cancer
Year: 2013, Volume: 52, Issue: 2, Pages: 150-155 |
| ISSN: | 1098-2264 |
| DOI: | 10.1002/gcc.22014 |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/gcc.22014 Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/gcc.22014 |
| Author Notes: | Itziar Salaverria, Idoia Martin-Guerrero, Birgit Burkhardt, Markus Kreuz, Thorsten Zenz, Ilske Oschlies, Norbert Arnold, Michael Baudis, Susanne Bens, Africa García-Orad, Jasmin Lisfeld, Carsten Schwaenen, Monika Szczepanowski, Swen Wessendorf, Michael Pfreundschuh, Lorenz Trümper, Wolfram Klapper, Reiner Siebert |
| Summary: | Translocations affecting chromosome subband 6p25.3 containing the IRF4 gene have been recently described as characteristic alterations in a molecularly distinct subset of germinal center B-cell-derived lymphomas. Secondary changes have yet only been described in few of these lymphomas. Here, we performed array-comparative genomic hybridization and molecular inversion probe microarray analyses on DNA from 12 formalin-fixed paraffin-embedded and two fresh-frozen IRF4 translocation-positive lymphomas, which together with the previously published data on nine cases allowed the extension of copy number analyses to a total of 23 of these lymphomas. All except one case carried chromosomal imbalances, most frequently gains in Xq28, 11q22.3-qter, and 7q32.1-qter and losses in 6q13-16.1, 15q14-22.31, and 17p. No recurrent copy-neutral losses of heterozygosity were observed. TP53 point mutations were detected in three of six cases with loss of 17p. Overall this study unravels a recurrent pattern of secondary genetic alterations in IRF4 translocation-positive lymphomas. © 2012 Wiley Periodicals, Inc. |
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| Item Description: | First published: 17 October 2012 Gesehen am 26.01.2022 |
| Physical Description: | Online Resource |
| ISSN: | 1098-2264 |
| DOI: | 10.1002/gcc.22014 |