Proto-Siqueira Rodrigo, Panepucci Rodrigo A, Careta Francisco P, Lee Abigail, Clear Andrew, Morris Kelly, Owen Carolyn, Rizzatti Edgar G, Silva Wilson A, Falcão Roberto P, Zago Marco A, Gribben John G
Hematology Division and Center for Cell-Based Therapy, Faculty of Medicine of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.
Blood. 2008 Jul 15;112(2):394-7. doi: 10.1182/blood-2007-11-124065. Epub 2008 Apr 23.
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.
为了鉴定参与慢性淋巴细胞白血病(CLL)分子发病机制的新基因,我们对CLL细胞进行了基因表达系列分析(SAGE),并将其与健康B细胞(nCD19(+))进行比较。我们发现CLL各亚型之间具有高度相似性,但CLL文库与nCD19(+)文库的比较显示,有55个基因在CLL中过度表达,49个基因在CLL中表达下调。基因本体分析显示,在Fas外源性凋亡途径上游发挥功能作用的TOSO在CLL细胞中过度表达。在78例CLL和12例nCD19(+)病例中,通过实时逆转录-聚合酶链反应证实了这一发现(P <.001)。我们使用流式细胞术和组织芯片验证了表达情况,并证明循环CLL细胞(P =.013)和淋巴结(P =.006)中TOSO蛋白增加了5.6倍。我们的SAGE结果表明,TOSO是CLL中一个新的过度表达的抗凋亡基因。