Alteration of SMRT tumor suppressor function in transformed non-Hodgkin lymphomas.

Abstract

Indolent non-Hodgkin lymphomas are characterized by a prolonged phase that is typically followed by a clinical progression associated with an accelerated clinical course and short survival time. Previous studies have not identified a consistent cytogenetic or molecular abnormality associated with transformation. The development of a transformed phenotype, evolving from the original low-grade component, most likely depends on multiple genetic events, including the activation of synergistic dominant oncogenes and a loss of tumor suppressor gene functions. Complex karyotypes and relatively bad chromosome morphology are typical of transformed non-Hodgkin lymphomas, rendering complete cytogenetic analysis difficult. Here, we report the use of transformed non-Hodgkin lymphoma cell lines and primary samples to identify the involvement of the silencing mediator of retinoic acid and thyroid hormone receptor (SMRT) gene that maps at chromosome 12q24 in transformed non-Hodgkin lymphomas. We also show that down-regulation of SMRT in the immortalized "Weinberg's model" cell lines induces transformation of the cells. Assessment of cDNA array profiles should further help us to design a working model for SMRT involvement in non-Hodgkin lymphoma transformation as a novel, nonclassical tumor suppressor.

• Authors: Lynda Song, Andrei Zlobin, Pushpankur Ghoshal, Qing Zhang, Christiane Houde, Sanne Weijzen, Qun Jiang, Elizabeth Nacheva, Danny Yagan, Eric Davis, Sylvie Galiegue-Zouitina, Daniel Catovsky, Thomas Grogan, Richard I Fisher, Lucio Miele, Lionel J Coignet
• Journal: Cancer research (Cancer Res) Vol. 65 Issue 11 Pg. 4554-61 (Jun 01 2005) ISSN: 0008-5472 [Print] United States
• PMID: 15930272 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• DNA-Binding Proteins
• Immunoglobulin J Recombination Signal Sequence-Binding Protein
• NCOR2 protein, human
• Nuclear Proteins
• Nuclear Receptor Co-Repressor 2
• RBPJ protein, human
• Repressor Proteins

Topics

• Apoptosis (genetics)
• Cell Line, Tumor
• Cell Transformation, Neoplastic (genetics, metabolism, pathology)
• Chromosomes, Human, Pair 12 (genetics)
• DNA-Binding Proteins (biosynthesis, genetics)
• Down-Regulation
• Gene Deletion
• Gene Rearrangement
• Genes, Tumor Suppressor
• Humans
• Immunoglobulin J Recombination Signal Sequence-Binding Protein
• Lymphoma, Non-Hodgkin (genetics, metabolism, pathology)
• Nuclear Proteins (genetics)
• Nuclear Receptor Co-Repressor 2
• Oligonucleotide Array Sequence Analysis
• Repressor Proteins (biosynthesis, genetics)
• Transcriptional Activation