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Specific peptide interference reveals BCL6 transcriptional and oncogenic mechanisms in B-cell lymphoma cells.

The BTB/POZ transcriptional repressor and candidate oncogene BCL6 is frequently misregulated in B-cell lymphomas. The interface through which the BCL6 BTB domain mediates recruitment of the SMRT, NCoR and BCoR corepressors was recently identified. To determine the contribution of this interface to BCL6 transcriptional and biological properties, we generated a peptide that specifically binds BCL6 and blocks corepressor recruitment in vivo. This inhibitor disrupts BCL6-mediated repression and establishment of silenced chromatin, reactivates natural BCL6 target genes, and abrogates BCL6 biological function in B cells. In BCL6-positive lymphoma cells, peptide blockade caused apoptosis and cell cycle arrest. BTB domain peptide inhibitors may constitute a novel therapeutic agent for B-cell lymphomas.

Pubmed ID: 15531890


  • Polo JM
  • Dell'Oso T
  • Ranuncolo SM
  • Cerchietti L
  • Beck D
  • Da Silva GF
  • Prive GG
  • Licht JD
  • Melnick A


Nature medicine

Publication Data

December 6, 2004

Associated Grants

  • Agency: NCI NIH HHS, Id: CA59936
  • Agency: NCI NIH HHS, Id: CA99982

Mesh Terms

  • Amino Acid Motifs
  • B-Lymphocytes
  • Blotting, Western
  • DNA-Binding Proteins
  • Fluorescent Antibody Technique
  • Gene Expression Regulation, Neoplastic
  • Genes, Regulator
  • Humans
  • Immunoprecipitation
  • Lymphoma, Large B-Cell, Diffuse
  • Mutation
  • Nuclear Proteins
  • Nuclear Receptor Co-Repressor 1
  • Nuclear Receptor Co-Repressor 2
  • Peptides
  • Protein Binding
  • Protein Structure, Tertiary
  • Proto-Oncogene Proteins
  • Repressor Proteins
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tumor Cells, Cultured