Song Ju Han, Cho Kyung-Min, Kim Hyeoung-Joon, Kim Yeo-Kyeoung, Kim Nan Young, Kim Hee-Je, Lee Tae-Hyang, Hwang Seung Yong, Kim Tae Sung
Division of Life Sciences, School of Life Sciences and Biotechnology, Korea University, Seoul, Republic of Korea.
Genome Research Center for Hematopoietic Diseases, Chonnam National University Hwasun Hospital, Hwasun, Republic of Korea.
Oncol Rep. 2015 Jul;34(1):488-94. doi: 10.3892/or.2015.3959. Epub 2015 May 7.
Although acute myeloid leukemia (AML) exhibits diverse responses to chemotherapy, patients harboring the t(8;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.
尽管急性髓系白血病(AML)对化疗表现出不同的反应,但携带t(8;21)易位的患者属于预后良好的风险组。然而,该亚组对基于阿糖胞苷的治疗更敏感的原因尚未阐明。在本研究中,我们分析了诊断为AML且伴有或不伴有t(8;21)的患者中阿糖胞苷代谢相关基因的表达水平,并研究了它们与基于阿糖胞苷治疗后的临床结局之间的相关性。在所研究的8个基因中,在测试人群和验证队列中,t(8;21)阳性患者的集中核苷转运体3(CNT3)基因表达明显高于其他患者(曼-惠特尼U检验中P<0.001;皮尔逊相关分析中P<0.002)。此外,在多变量和单变量分析中,CNT3表达处于较高三分位数的t(8;21)阳性患者与CNT3表达处于较低三分位数的t(8;21)阳性患者相比,无病生存期更长[风险比(HR),0.117;95%置信区间(CI),0.025 - 0.557;P = 0.008],总生存期也更长(HR,0.062;95%CI,0.007 - 0.521;P = 0.010)。值得注意的是,这些趋势在t(8;21)阴性患者中并未出现。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) AML患者的临床结局。这表明CNT3表达可用于优化AML患者的治疗策略。