Expression of B-cell transcription factors in primary cutaneous B-cell lymphoma

Mod Pathol. 2006 Sep;19(9):1270-6. doi: 10.1038/modpathol.3800650. Epub 2006 Jun 16.

Abstract

Expression patterns of eight transcription factors involved in different stages of B-cell development were investigated in a large group of primary cutaneous B-cell lymphomas and compared with expression patterns during normal B-cell development. The following transcription factors were investigated: Pax-5, PU.1, Oct2, BOB.1, Bcl-6, Mum1/IRF4, Blimp-1 and FOXP1. Primary cutaneous large B-cell lymphomas, leg type showed aberrant coexpression of Bcl-6 and Mum1/IRF4 and in addition strong expression of FOXP1. Expression of FOXP1 and Mum1/IRF4 strongly suggests an activated B-cell type of origin. In contrast, primary cutaneous follicle center lymphomas showed expression of Bcl-6, Pax-5, PU.1, Oct2 and BOB.1, but not of Mum1/IRF4, Blimp-1 and FOXP1. Primary cutaneous marginal zone B-cell lymphoma showed expression of Pax-5, PU.1, Oct2 and BOB.1, but not Bcl-6 by the neoplastic B-cells, and Mum1/IRF4 and Blimp-1 by the neoplastic plasma cells. In conclusion, in primary cutaneous follicle center lymphoma and primary cutaneous marginal zone B-cell lymphoma expression patterns were observed similar to their supposed benign counterparts, germinal center B-cells and postgerminal center B-cells, respectively, which might reflect their indolent clinical behaviour and excellent prognosis. In contrast, the activated B-cell expression pattern in the group of primary cutaneous large B-cell lymphoma, leg type may contribute to its poor prognosis and Mum1/IRF4 and FOXP1 may serve as additional diagnostic markers for this type of primary cutaneous B-cell lymphoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • B-Lymphocytes / cytology
  • B-Lymphocytes / metabolism*
  • Biomarkers, Tumor / biosynthesis
  • Biopsy
  • DNA-Binding Proteins / biosynthesis
  • Fluorescent Antibody Technique, Indirect
  • Forkhead Transcription Factors / biosynthesis
  • Germinal Center / metabolism
  • Germinal Center / pathology
  • Humans
  • Immunoenzyme Techniques
  • Interferon Regulatory Factors / biosynthesis
  • Lymphoma, B-Cell / metabolism*
  • Lymphoma, B-Cell / pathology
  • Octamer Transcription Factor-2 / biosynthesis
  • PAX5 Transcription Factor / biosynthesis
  • Palatine Tonsil / metabolism
  • Palatine Tonsil / pathology
  • Proto-Oncogene Proteins / biosynthesis
  • Proto-Oncogene Proteins c-bcl-6
  • Repressor Proteins / biosynthesis
  • Skin Neoplasms / metabolism*
  • Skin Neoplasms / pathology
  • Trans-Activators / biosynthesis
  • Transcription Factors / biosynthesis*

Substances

  • BCL6 protein, human
  • Biomarkers, Tumor
  • DNA-Binding Proteins
  • FOXP1 protein, human
  • Forkhead Transcription Factors
  • Interferon Regulatory Factors
  • Octamer Transcription Factor-2
  • PAX5 Transcription Factor
  • PAX5 protein, human
  • POU2AF1 protein, human
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-bcl-6
  • Repressor Proteins
  • Trans-Activators
  • Transcription Factors
  • interferon regulatory factor-4
  • proto-oncogene protein Spi-1