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NOTCH1 Activation Negatively Impacts on Chronic Lymphocytic Leukemia Outcome and Is Not Correlated to the NOTCH1 and IGHV Mutational Status

机译:Notch1激活对慢性淋巴细胞白血病结果产生负面影响,与Notch1和IghV突变状态无关

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摘要

NOTCH1 mutations and deregulated signal have been commonly found in chronic lymphocytic leukemia (CLL) patients. Whereas the impact of NOTCH1 mutations on clinical course of CLL has been widely studied, the prognostic role of NOTCH1 activation in CLL remains to be defined. Here, we analyzed the activation of NOTCH1/NOTCH2 (ICN1/ICN2) and the expression of JAGGED1 (JAG1) in 163 CLL patients and evaluated their impact on TTFT (Time To First Treatment) and OS (Overall Survival). NOTCH1 activation (ICN1+) was found in 120/163 (73.6%) patients. Among them, 63 (52.5%) were NOTCH1 mutated (ICN1+/mutated) and 57 (47.5%) were NOTCH1 wild type (ICN1+/WT). ICN1+ patients had a significant reduction of TTFT compared to ICN1-negative (ICN1−). In the absence of NOTCH1 mutations, we found that the ICN1+/WT group had a significantly reduced TTFT compared to ICN1− patients. The analysis of IGHV mutational status showed that the distribution of the mutated/unmutated IGHV pattern was similar in ICN1+/WT and ICN1− patients. Additionally, TTFT was significantly reduced in ICN1+/ICN2+ and ICN1+/JAG1+ patients compared to ICN1−/ICN2− and ICN1−/JAG1− groups. Our data revealed for the first time that NOTCH1 activation is a negative prognosticator in CLL and is not correlated to NOTCH1 and IGHV mutational status. Activation of NOTCH2 and JAGGED1 expression might also influence clinical outcomes in this group, indicating the need for further dedicated studies. The evaluation of different NOTCH network components might represent a new approach to refine CLL risk stratification.
机译:在慢性淋巴细胞白血病(CLL)患者中常见于Notch1突变和令人讨调的信号。然而,在CLL临床过程中对Notch1突变的影响已被广泛研究,但Notch1激活在CLL中的预后作用仍有待定义。在这里,我们分析了Notch1 / Notch2(ICN1 / ICN2)的激活和jagged1(Jag1)的表达,在163例CLL患者中表达并评估它们对TTFT的影响(时间至第一次处理)和OS(总存活)。在120/163(73.6%)患者中发现了Notch1活化(ICN1 +)。其中,63(52.5%)是Notch1突变(ICN1 + /突变),57(47.5%)均未脱苯(ICN1 + / WT)。与ICN1阴性(ICN1-)相比,ICN1 +患者的TTFT显着减少了TTFT。在没有Notch1突变的情况下,我们发现ICN1 + / WT组与ICN1患者相比具有显着降低的TTFT。 IGHV突变状态的分析表明,ICN1 + / WT和ICN1患者的突变/未传统IGHV模式的分布类似。另外,与ICN1 / ICN2和ICN1-/ JAG1-组相比,ICN1 + / ICN2 +和ICN1 + / JAG1 +患者中TTFT显着降低。我们的数据显示第一次Notch1激活是CLL中的负预测器,与Notch1和IghV突变状态无关。 Notch2和Jagged1表达的激活也可能影响该组中的临床结果,表明需要进一步专用研究。不同缺口网络组件的评估可能代表一种改进CLL风险分层的新方法。

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