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Neoplasia: SAGE analysis demonstrates increased expression of TOSO contributing to Fas-mediated resistance in CLL

机译:瘤形成:SAGE分析表明TOSO的表达增加有助于CLL中Fas介导的耐药性

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摘要

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.
机译: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细胞中的基因表达(SAGE)进行了系列分析,并将其与健康的B细胞(nCD19 + )进行了比较。我们发现CLL亚型之间具有高度相似性,但是CLL与nCD19 + 文库的比较显示,有55个基因被过度代表,而49个基因在CLL中被下调。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细胞中过表达。实时逆转录聚合酶链反应在78例CLL和12例nCD19 + 病例中得到了证实(P <.001)。我们使用流式细胞仪和组织芯片验证了表达,并证明了循环CLL细胞(P = .013)和淋巴结(P = .006)中TOSO蛋白的增加5.6倍。我们的SAGE结果表明,TOSO是CLL中一个新的过表达的抗凋亡基因。

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