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Concentrative nucleoside transporter 3 as a prognostic indicator for favorable outcome of t(8;21)-positive acute myeloid leukemia patients after cytarabine-based chemotherapy

机译:浓缩核苷转运蛋白3作为t(8; 21)阳性的急性髓性白血病患者在阿糖胞苷基础上化疗后预后良好的预后指标

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摘要

Although acute myeloid leukemia (AML) exhibits diverse responses to chemotherapy, patients harboring the 48;21) translocation are part of a favorable risk group. However, the reason why this subgroup is more responsive to cytarabine-based therapy has not been elucidated. In the present study, we analyzed expression levels of cytarabine metabolism-related genes in patients diagnosed with AML with or without t(8;21) and investigated their correlation with clinical outcomes after cytarabine-based therapy. Among the 8 genes studied, expression of the concentrative nucleoside transporter 3 (CNT3) gene was significantly higher in t(8;21)positive patients compared to the others in the test population and the validation cohort (P<0.001 in Mann-Whitney U test; P<0.002 in Pearson's correlation analysis). Additionally, in both multivariate and univariate analyses, t(8;21)-positive patients categorized in a higher CNT3 expression tertile had longer disease-free survival [hazard ratio (HR), 0.117; 95% confidence interval (CI), 0.025-0.557; P=0.008] and overall survival (HR, 0.062; 95% CI, 0.007-0.521; P=0.010) compared to t(8;21)-positive patients in a lower CNT3 expression tertile. Notably, these trends did not occur in t(8;21)-negative patients. Our results demonstrate that CNT3 expression is associated with overall favorable outcomes and is predictive of clinical outcomes in AML patients with t(8;21). This suggests that CNT3 expression can be used to optimize treatment strategies for AML patients.
机译:尽管急性髓细胞性白血病(AML)对化学疗法表现出多种反应,但是具有48; 21)易位的患者是一个有利的危险人群。但是,该亚组对基于阿糖胞苷的治疗反应更敏感的原因尚未阐明。在本研究中,我们分析了患有或不患有t(8; 21)的AML患者中阿糖胞苷代谢相关基因的表达水平,并研究了它们与阿糖胞苷治疗后临床疗效的相关性。在研究的8个基因中,t(8; 21)阳性患者中集中核苷转运蛋白3(CNT3)基因的表达显着高于测试人群和验证队列中的其他患者(Mann-Whitney U中P <0.001)检验;在Pearson相关分析中P <0.002)。另外,在多变量和单变量分析中,分类为CNT3表达较高的三分位数较高的t(8; 21)阳性患者的无病生存期更长[危险比(HR),0.117; 10%。 95%置信区间(CI),0.025-0.557; P = 0.008]和总生存率(HR,0.062; 95%CI,0.007-0.521; P = 0.010)与CNT3表达较低的t(8; 21)阳性患者相比。值得注意的是,这些趋势在t(8; 21)阴性患者中并未发生。我们的结果表明,CNT3表达与总体良好预后相关,并且可预测t(8; 21)的AML患者的临床预后。这表明CNT3表达可用于优化AML患者的治疗策略。

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