Abnormal PcG protein expression in Hodgkin's lymphoma. Relation with E2F6 and NFkappaB transcription factors

• Published in: The Journal of pathology 2004-12, Vol.204 (5), p.528-537
• Main Authors: Sánchez-Beato, Margarita, Sánchez, Esther, García, Juan F, Pérez-Rosado, Alberto, Montoya, María C, Fraga, Mario, Artiga, M Jesús, Navarrete, Mercedes, Abraira, Víctor, Morente, Manuel, Esteller, Manel, Koseki, Haruhiko, Vidal, Miguel, Piris, Miguel A
• Format: Article
• Language: English
• Subjects: Apoptosis - genetics; B-Lymphocytes - metabolism; Blotting, Western - methods; Cell Cycle - genetics; Cell Cycle Proteins - genetics; Cell Differentiation - genetics; DNA-Binding Proteins - analysis; DNA-Binding Proteins - genetics; E2F Transcription Factors; E2F6 Transcription Factor; Electrophoresis, Capillary - methods; Fluorescent Antibody Technique - methods; Hodgkin Disease - genetics; Hodgkin Disease - metabolism; Humans; Immunohistochemistry - methods; Intracellular Signaling Peptides and Proteins - analysis; Lymphoid Tissue - metabolism; NF-kappa B - genetics; Nuclear Proteins - analysis; Polycomb Repressive Complex 1; Polycomb-Group Proteins; Proto-Oncogene Proteins - analysis; Repressor Proteins - analysis; Transcription Factors - genetics; Ubiquitin-Protein Ligases; Zinc Fingers
• ISSN: 0022-3417

The Polycomb group (PcG) of proteins comprises a family of repressors of homeobox genes that play key roles in body formation, haematopoiesis and cell cycle control. In this study, a large-scale analysis of PcG protein expression (BMI1, MEL18, PH1, RNF2, RING1, and RYBP) was performed in 321 Hodgkin's lymphoma (HL) biopsies and in reactive lymphoid tissues using tissue microarrays. The relevance of PcG proteins in HL was also investigated by the simultaneous analysis of PcG and other proteins involved in the control of cell cycle, transcription machinery and lymphoid differentiation. The analysis revealed increased expression of a set of PcG proteins (particularly RYBP and BMI1) in tumour cells in comparison with reactive lymphoid tissue. One of the most striking findings was anomalous RYBP expression in 55% of classical HL cases associated with an unfavourable response to treatment and shorter survival. The data obtained in this study also show an association of PcG proteins with E2F6 and NFkappaB transcription factors. The statistical relationship between PcG and NFkappaB activation was further explored in HL-derived cell lines treated with curcumin, an NFkappaB inhibitor, and TNFalpha. Up- or downregulation of MEL18 was paralleled by loss or gain of activated NFkappaB, which suggests that NFkappaB may regulate expression of this protein. Investigation of the relationship between E2F6 and RING1 by immunofluorescence and confocal analysis, in HL cell lines and paraffin sections, revealed co-expression of both proteins in the same tumour cells. These results allow us to propose that the formation of transcription complexes with E2F6 may modify the functional status of PcG proteins in HSR cells.