microRNA-100和-196b作为儿童急性淋巴细胞白血病血液标志物的诊断意义

Aya M. Mohamed, Nashwa El-Khazragy, M. M. Said, M. Swellam, A. Esmat
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摘要

本研究旨在探讨miRNA-100和-196b在儿童急性淋巴细胞白血病(ALL)及其表型中的相对表达水平。从40例小儿ALL患者和10例健康对照者的外周血中分离外周血单个核细胞(pmnc)。采用定量实时聚合酶链反应(qRT-PCR)法检测miRNA-100和-196b的表达水平。据报道,与正常对照组相比,ALL患者中miRNA-100和-196b的表达水平显著上调。T-ALL患者miRNA-100和196b的表达高于b -ALL前期和双表型ALL患者。MiRNA-100和-196b区分ALL患者和正常对照的临界值分别为6.54(92.5%敏感性,100%特异性)和5.49(92.5%敏感性,100%特异性)。此外,miRNA-100和-196b在ALL不同表型之间具有较高的敏感性、特异性和准确性。在ALL患者中,miRNA-100与-196b表达水平呈显著正相关(r = 0.328, p < 0.05), miRNA-100表达水平与血小板计数呈显著负相关(r = -0.448, p < 0.01)。我们的研究结果表明,miRNA-100和-196b可以被认为是诊断ALL和区分其表型的良好的无创血液生物标志物。
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Diagnostic significance of microRNA-100 and -196b as blood markers for acute lymphoblastic leukemia among children
Article history: Received 15 September 2019 Accepted 21 October 2019 The present study was undertaken to investigate the relative expression levels of miRNA-100 and -196b in childhood acute lymphoblastic leukemia (ALL) and its phenotypes. Peripheral blood mononuclear cells (PMNCs) were isolated from peripheral blood samples of 40 pediatric ALL patients and 10 healthy controls. We assessed the expression levels of miRNA-100 and -196b by quantitative real time polymerase chain reaction (qRT-PCR) assay. A significant upregulation in the expression levels of miRNA-100 and -196b in ALL patients is reported, compared to the normal controls. T-ALL patients manifested a higher expression of miRNA-100 and-196b than those with pre-B-ALL and biphenotypic ALL. MiRNA-100 and -196b distinguished ALL patients from the normal controls at cut-off values 6.54 (92.5 % sensitivity, 100 % specificity) and 5.49 (92.5 % sensitivity, 100 % specificity), respectively. As well, miRNA-100 and -196b discriminated between the different ALL phenotypes with high sensitivity, specificity and accuracy levels. Two correlation coefficients are herein reported including a significant positive correlation between miRNA-100 and -196b expression levels (r = 0.328, p < 0.05) and a significant negative correlation between miRNA-100 expression level and the platelets count (r = -0.448, p < 0.01) in ALL patients. Our findings concluded that miRNA-100 and -196b could be considered as good noninvasive blood biomarkers for the diagnosis of ALL, and in distinguishing its phenotypes.
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