Lu Xiao-Jing, Jiang Qian, Huang Peng-Li, Li Gang, Zhang Wen-Juan, Zhao Xiao-Xi, Zheng Hu-Yong
Capital Medical University, Beijing, China.
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2013 Feb;21(1):68-72. doi: 10.7534/j.issn.1009-2137.2013.01.015.
This study was aimed to investigate the expression of plasma miR-223 in pediatric acute lymphoblastic leukemia (ALL) in different treatment time point. A total of 64 pediatric ALL samples were selected from patients treated in Beijing Children's Hospital from May 2005 to January 2012, including 30 samples at new diagnosis (ND), 30 samples at complete remission (CR) and 4 samples at relapse. Without RNA extraction, the miR-223 levels in plasma were directly detected by a reverse-transcription quantitative real-time PCR assay. The results indicated that the expression of plasma miR-223 in pediatric ALL was lower at ND but elevated after CR. The miR-223 expression in plasma of relapse patients didn't show significant difference probably due to a few cases of relapse. The miR-223 levels in plasma had not displayed significant difference between TEL-AML1 positive patients and no fusion gene B lineage ALL patients either at ND or at CR. It is concluded that the plasma miR-223 decreases at ND and increases in CR of children with ALL. miR-223 may act as an anti-oncogene and may be taken as a potential predictive biomarker for evaluating the therapeutic effect of leukemia.
本研究旨在探讨不同治疗时间点小儿急性淋巴细胞白血病(ALL)患者血浆miR-223的表达情况。选取2005年5月至2012年1月在北京儿童医院接受治疗的64例小儿ALL患者样本,其中初诊(ND)样本30例、完全缓解(CR)样本30例、复发样本4例。无需提取RNA,采用逆转录定量实时PCR法直接检测血浆中miR-223水平。结果显示,小儿ALL患者血浆miR-223在ND时表达较低,但CR后升高。复发患者血浆中miR-223表达可能因复发病例较少未显示出显著差异。在ND或CR时,TEL-AML1阳性患者与无融合基因B系ALL患者血浆中miR-223水平也未显示出显著差异。结论为小儿ALL患者血浆miR-223在ND时降低,在CR时升高。miR-223可能作为一种抑癌基因,可作为评估白血病治疗效果的潜在预测生物标志物。