Immunohistochemical expression of Mum-1, Oct-2 and Bcl-6 in systemic anaplastic large cell lymphomas

Tumori. 2011 Sep-Oct;97(5):634-8. doi: 10.1177/030089161109700516.

Abstract

Aims and background: Several transcription factors predominantly used for B-cell lineage identification are also expressed in a small percentage of T cells within germinal centers and interfollicular areas. The aim of the study was to evaluate the expression of Mum-1, Oct-2 and Bcl-6 in systemic anaplastic large cell lymphoma.

Methods: Thirty cases of anaplastic large cell lymphoma were retrieved from our archives and tissue microarray constructed. Immunohistochemistry was carried out using an avidin-biotin peroxidase complex method.

Results: A predominance of nuclear staining was observed for all transcription factors. Mum-1 was positive in all but one case (96.7%). Half of the cases displayed Oct-2 expression (15/30 cases). A considerable number of cases also had Bcl-6 expression (9/30). Bcl-6 staining was noted to be more common in ALK positive cases.

Conclusion: Our findings emphasize that these markers are not restricted to B-cell lineage and that extensive expression can be observed in anaplastic large cell lymphoma of T/null cell phenotype.

MeSH terms

  • Anaplastic Lymphoma Kinase
  • Biomarkers, Tumor / analysis*
  • DNA-Binding Proteins / analysis*
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Immunohistochemistry
  • Interferon Regulatory Factors / analysis*
  • Lymphoma, Large-Cell, Anaplastic / chemistry*
  • Lymphoma, Large-Cell, Anaplastic / pathology
  • Octamer Transcription Factor-2 / analysis*
  • Proto-Oncogene Proteins c-bcl-6
  • Receptor Protein-Tyrosine Kinases / analysis*
  • Tissue Array Analysis

Substances

  • BCL6 protein, human
  • Biomarkers, Tumor
  • DNA-Binding Proteins
  • Interferon Regulatory Factors
  • Octamer Transcription Factor-2
  • POU2F2 protein, human
  • Proto-Oncogene Proteins c-bcl-6
  • interferon regulatory factor-4
  • ALK protein, human
  • Anaplastic Lymphoma Kinase
  • Receptor Protein-Tyrosine Kinases