| Literature DB >> 18434611 |
Rodrigo Proto-Siqueira1, Rodrigo A Panepucci, Francisco P Careta, Abigail Lee, Andrew Clear, Kelly Morris, Carolyn Owen, Edgar G Rizzatti, Wilson A Silva, Roberto P Falcão, Marco A Zago, John G Gribben.
Abstract
To identify novel genes involved in the molecular pathogenesis of chronic lymphocytic leukemia (CLL) we performed a serial analysis of gene expression (SAGE) in CLL cells, and compared this with healthy B cells (nCD19(+)). We found a high level of similarity among CLL subtypes, but a comparison of CLL versus nCD19(+) libraries revealed 55 genes that were over-represented and 49 genes that were down-regulated in CLL. A gene ontology analysis revealed that TOSO, which plays a functional role upstream of Fas extrinsic apoptosis pathway, was over-expressed in CLL cells. This finding was confirmed by real-time reverse transcription-polymerase chain reaction in 78 CLL and 12 nCD19(+) cases (P < .001). We validated expression using flow cytometry and tissue microarray and demonstrated a 5.6-fold increase of TOSO protein in circulating CLL cells (P = .013) and lymph nodes (P = .006). Our SAGE results have demonstrated that TOSO is a novel over-expressed antiapoptotic gene in CLL.Entities:
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Year: 2008 PMID: 18434611 PMCID: PMC2442748 DOI: 10.1182/blood-2007-11-124065
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113