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High Expression of Suppressor of Cytokine Signaling-2 Predicts Poor Outcome in Pediatric Acute Myeloid Leukemia: A Report from the Childrens Oncology Group

机译:细胞因子信号2抑制剂的高表达预测小儿急性髓细胞性白血病的结果差:儿童肿瘤学组的一份报告。

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摘要

Deregulated cytokine signaling is a characteristic feature of acute myeloid leukemia (AML), and expression signatures of cytokines and chemokines have been identified as significant prognostic factor in this disease. Given this aberrant signaling, we hypothesized that expression of Suppressor of Cytokine Signaling-2 (SOCS2), a negative regulator of cytokine signaling, might be altered in AML and could provide predictive information. Among 188 participants of the Children's Oncology Group AAML03P1 trial, SOCS2 mRNA levels varied >6,000-fold. Higher (>median) SOCS2 expression was associated with inferior overall (60±10% vs. 75±9%, p=0.026) and event-free (44±10% vs. 59±10%, p=0.031) survival. However, these differences were accounted for by higher prevalence of high-risk and lower prevalence of low-risk disease among patients with higher SOCS2 expression, limiting the clinical utility of SOCS2 as predictive marker. It remains untested whether high SOCS2 expression identifies a subset of leukemias with deregulated cytokine signaling that could be amenable to therapeutic intervention.
机译:细胞因子信号转导失调是急性髓细胞性白血病(AML)的特征,细胞因子和趋化因子的表达特征已被鉴定为该疾病的重要预后因素。鉴于这种异常的信号传导,我们假设细胞因子信号传导的负调节剂细胞因子信号传导抑制因子2(SOCS2)的表达可能在AML中发生改变,并可能提供预测信息。在儿童肿瘤学小组AAML03P1试验的188名参与者中,SOCS2 mRNA水平变化> 6,000倍。较高(>中位数)的SOCS2表达与总体生存率较低(60±10%比75±9%,p = 0.026)和无事件生存(44±10%对59±10%,p = 0.031)相关。但是,这些差异是由于SOCS2表达较高的患者中高危患病率较高而低危疾病患病率较低,限制了SOCS2作为预测标志物的临床应用。高SOCS2的表达是否能识别出细胞因子信号转导异常的白血病子集尚待检验,这可能适合治疗性干预。

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