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.
%0 Journal Article
%1 Salaverria.2013
%A Salaverria, Itziar
%A Martin-Guerrero, Idoia
%A Burkhardt, Birgit
%A Kreuz, Markus
%A Zenz, Thorsten
%A Oschlies, Ilske
%A Arnold, Norbert
%A Baudis, Michael
%A Bens, Susanne
%A García-Orad, Africa
%A Lisfeld, Jasmin
%A Schwaenen, Carsten
%A Szczepanowski, Monika
%A Wessendorf, Swen
%A Pfreundschuh, Michael
%A Trümper, Lorenz
%A Klapper, Wolfram
%A Siebert, Reiner
%D 2013
%J Genes, chromosomes & cancer
%K Adolescent Adult Aged Aged,_80_and_over Base_Sequence Child Child,_Preschool Chromosome_Aberrations Comparative_Genomic_Hybridization/methods DNA_Copy_Number_Variations DNA_Mutational_Analysis Female Germinal_Center/metabolism/pathology Humans In_Situ_Hybridization,_Fluorescence Interferon_Regulatory_Factors/genetics Lymphoma,_Follicular/genetics/metabolism/pathology Lymphoma,_Large_B-Cell,_Diffuse/genetics/pathology Male Middle_Aged Point_Mutation Translocation,_Genetic Tumor_Suppressor_Protein_p53/genetics Young_Adult
%N 2
%P 150–155
%T High resolution copy number analysis of IRF4 translocation-positive diffuse large B-cell and follicular lymphomas
%V 52
%X 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.
@article{Salaverria.2013,
abstract = {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.},
added-at = {2014-10-13T18:24:59.000+0200},
author = {Salaverria, Itziar and Martin-Guerrero, Idoia and Burkhardt, Birgit and Kreuz, Markus and Zenz, Thorsten and Oschlies, Ilske and Arnold, Norbert and Baudis, Michael and Bens, Susanne and García-Orad, Africa and Lisfeld, Jasmin and Schwaenen, Carsten and Szczepanowski, Monika and Wessendorf, Swen and Pfreundschuh, Michael and Trümper, Lorenz and Klapper, Wolfram and Siebert, Reiner},
biburl = {https://www.bibsonomy.org/bibtex/286560098433d308893bdc96a8e6b3e76/drtester},
interhash = {0fe1c8a9288521726da7233732669787},
intrahash = {86560098433d308893bdc96a8e6b3e76},
journal = {Genes, chromosomes \& cancer},
keywords = {Adolescent Adult Aged Aged,_80_and_over Base_Sequence Child Child,_Preschool Chromosome_Aberrations Comparative_Genomic_Hybridization/methods DNA_Copy_Number_Variations DNA_Mutational_Analysis Female Germinal_Center/metabolism/pathology Humans In_Situ_Hybridization,_Fluorescence Interferon_Regulatory_Factors/genetics Lymphoma,_Follicular/genetics/metabolism/pathology Lymphoma,_Large_B-Cell,_Diffuse/genetics/pathology Male Middle_Aged Point_Mutation Translocation,_Genetic Tumor_Suppressor_Protein_p53/genetics Young_Adult},
number = 2,
pages = {150–155},
timestamp = {2014-10-13T18:24:59.000+0200},
title = {High resolution copy number analysis of IRF4 translocation-positive diffuse large B-cell and follicular lymphomas},
volume = 52,
year = 2013
}