Relationship between REL amplification, REL function, and clinical and biologic features in diffuse large B-cell lymphomas Journal Article

Authors: Houldsworth, J.; Olshen, A. B.; Cattoretti, G.; Donnelly, G. B.; Teruya-Feldstein, J.; Qin, J.; Palanisamy, N.; Shen, Y.; Dyomina, K.; Petlakh, M.; Pan, Q.; Zelenetz, A. D.; Dalla-Favera, R.; Chaganti, R. S. K.
Article Title: Relationship between REL amplification, REL function, and clinical and biologic features in diffuse large B-cell lymphomas
Abstract: Although it has been suggested that REL is the critical target gene of 2p12-16 amplification in diffuse large B-cell lymphoma (DLBCL), little experimental evidence supports this notion. In the present study, we sought to evaluate the relationship between REL amplification and REL function in a panel of 46 newly diagnosed DLBCLs and to correlate with DLBCL subgroups as identified by gene expression profiles and clinical features. The results Indicate that amplification of the REL locus is not associated with accumulation of the active form of REL, as evaluated by immunofluorescence analysis. Upon subgrouping of the DLBCL cases based on gene expression signatures, REL amplification was detected in all subgroups, while high levels of nuclear-located REL were more frequently detected in activated B-cell-like DLBCL. Correlative analyses of REL copy number and REL nuclear accumulation with clinical parameters did not reveal any significant associations. Together these results indicate that 2p12-16 amplification does not lead to abnormal REL activation, suggesting that REL may not be the functional target of the amplification event. Nonetheless, these data indicate that DLBCLs are heterogeneous with respect to REL and thus nuclear factor-κB (NF-κB) activity. © 2004 by The American Society of Hematology.
Keywords: adult; clinical article; human tissue; aged; aged, 80 and over; middle aged; gene; in situ hybridization, fluorescence; disease association; gene amplification; gene expression; gene function; immunoglobulin enhancer binding protein; immunofluorescence; rna; b cell lymphoma; gene expression regulation, neoplastic; reverse transcriptase polymerase chain reaction; nf-kappa b; translocation, genetic; microscopy, fluorescence; cell nucleus; large cell lymphoma; karyotyping; proto-oncogene proteins c-rel; lymphoma, large-cell, diffuse; blotting, southern; humans; human; male; female; priority journal; article; rel gene; genes, rel
Journal Title: Blood
Volume: 103
Issue: 5
ISSN: 0006-4971
Publisher: American Society of Hematology  
Date Published: 2004-03-01
Start Page: 1862
End Page: 1868
Language: English
DOI: 10.1182/blood-2003-04-1359
PROVIDER: scopus
PUBMED: 14615382
Notes: Blood -- Cited By (since 1996):52 -- Export Date: 16 June 2014 -- CODEN: BLOOA -- Source: Scopus
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MSK Authors
  1. Yingjing Shen
    2 Shen
  2. Julie T Feldstein
    288 Feldstein
  3. Jing Qin
    86 Qin
  4. Andrew D Zelenetz
    554 Zelenetz
  5. Adam B Olshen
    107 Olshen
  6. Raju S K Chaganti
    266 Chaganti
  7. Ekaterina Matveevna Dyomina
    13 Dyomina
  8. Qiulu Pan
    11 Pan