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      NFκB expression is a feature of both activated B-cell-like and germinal center B-cell-like subtypes of diffuse large B-cell lymphoma.

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          Abstract

          The activation of nuclear factor kappa B (NFκB) transcription factor family is considered to have a key role in diffuse large B-cell lymphoma (DLBCL) pathogenesis and is associated with a specific molecular subtype, the activated B-cell-like (ABC) subtype. We evaluated the expression of NFκB by immunohistochemistry in a large series of DLBCL cases. The five different NFκB family members (NFκB1, NFκB2, RELA, RELB, and REL) showed a heterogeneous expression pattern with the vast majority of cases being positive for at least one factor. Two independent series of tumor samples were classified into germinal center B-cell-like (GCB) or ABC subtypes using different approaches, immunohistochemistry, or gene expression profiling, and the expression of NFκB family members was assessed. Notably, no significant differences regarding the expression of the different NFκB members were detected between the two subtypes, suggesting that NFκB signaling is a prominent feature not only in the ABC subtype, but also in the GCB tumors. Of the five transcription factors, only REL expression had a significant clinical impact on R-CHOP-treated diffuse large B-cell lymphoma, identifying a subgroup of patients with superior clinical outcome.

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          Author and article information

          Journal
          Mod. Pathol.
          Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
          1530-0285
          0893-3952
          Oct 2014
          : 27
          : 10
          Affiliations
          [1 ] 1] Molecular Pathology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain [2] Cancer Genomics Group, Valdecilla Biomedical Research Institute (IFIMAV), Santander, Spain.
          [2 ] Pathology Department, Hospital Universitario Marques de Valdecilla, Universidad de Cantabria, IFIMAV, Santander, Spain.
          [3 ] UT MD Anderson Cancer Center, Houston, TX, USA.
          [4 ] Cancer Genomics Group, Valdecilla Biomedical Research Institute (IFIMAV), Santander, Spain.
          [5 ] Biotechnology Programme, CNIO; Madrid, Spain.
          [6 ] Hospital Virgen de la Salud, Toledo, Spain.
          [7 ] Hospital Central de Asturias, Oviedo, Spain.
          [8 ] Hospital Vall d'Hebron, Barcelona, Spain.
          [9 ] Oncology-Hematology Area, Instituto Investigación Sanitaria Hospital Universitario Puerta de Hierro-Majadahonda, Calle Joaquín Rodrígo 2, Madrid, Spain.
          [10 ] 1] Cancer Genomics Group, Valdecilla Biomedical Research Institute (IFIMAV), Santander, Spain [2] Pathology Department, Hospital Universitario Marques de Valdecilla, Universidad de Cantabria, IFIMAV, Santander, Spain.
          Article
          modpathol201434
          10.1038/modpathol.2014.34
          24603590
          8cad3ced-28d4-4118-9a85-1996faa3a672
          History

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