Department of Hematology, The First Hospital, China Medical University, Shenyang, Liaoning, China (mainland).
Med Sci Monit. 2017 Oct 5;23:4768-4778. doi: 10.12659/msm.902689.
BACKGROUND MicroRNAs (miRNAs) play an important role in the development and progression of acute myeloid leukemia (AML). The miR-148/152 family has been reported to be express differently in various kinds of tumors. We investigated the expression level of the miR-148/152 family in AML patients and their clinical significance. MATERIAL AND METHODS Expression levels of the miR-148/152 family in 80 patients with newly diagnosed AML and 20 healthy participants were analyzed by qRT-PCR. We also evaluated the relationship between the expression levels of the miR-148/152 family and clinicopathological features of AML patients. RESULTS Compared with healthy controls, we found a significant lower expression of downregulated miR-148/152 in AML patients (p<0.0001). The expression of miR148/152 family was associated with various AML clinicopathological risk parameters including FAB classifications, cytogenetics, and gene mutations. The number of patients with high expression levels of miR-148a/b was significantly increased in the low-risk group and significantly decreased in the high-risk group. (p=0.025, p=0.000, respectively). Patients with higher expression of miR-148b showed a higher complete remission (CR) rate (p=0.043). Importantly, higher expression of miR-148a/b was correlated with lower relapse rate (p=0.035, p=0.027, respectively) and showed a longer relapse-free survival (RFS) (p=0.0321, p=0.002, respectively). In the subgroup analysis, RFS was significantly affected by the expression of miR-148a/b in patients the high and the intermediate-risk groups (p=0.0499, p=0.0114, respectively). CONCLUSIONS The expression levels of the miR-148/152 family were lower in patients with AML compared to healthy controls, and were associated with various AML clinicopathological parameters and therapeutic effect. The miR-148/152 family may prove to be a new biomarker for AML.
微小 RNA(miRNAs)在急性髓系白血病(AML)的发展和进展中发挥着重要作用。miR-148/152 家族已被报道在各种肿瘤中表达不同。我们研究了 AML 患者中 miR-148/152 家族的表达水平及其临床意义。
采用 qRT-PCR 分析 80 例初诊 AML 患者和 20 例健康对照者 miR-148/152 家族的表达水平。还评估了 miR-148/152 家族的表达水平与 AML 患者临床病理特征的关系。
与健康对照组相比,我们发现 AML 患者下调的 miR-148/152 表达明显降低(p<0.0001)。miR148/152 家族的表达与 AML 临床病理风险参数有关,包括 FAB 分类、细胞遗传学和基因突变。miR-148a/b 高表达的患者在低危组中的数量显著增加,而在高危组中则显著减少(p=0.025,p=0.000)。miR-148b 高表达的患者完全缓解(CR)率更高(p=0.043)。重要的是,miR-148a/b 高表达与较低的复发率相关(p=0.035,p=0.027),且无复发生存(RFS)较长(p=0.0321,p=0.002)。在亚组分析中,miR-148a/b 的表达在高危和中危组患者的 RFS 中均有显著影响(p=0.0499,p=0.0114)。
AML 患者 miR-148/152 家族的表达水平低于健康对照组,与 AML 临床病理参数和治疗效果有关。miR-148/152 家族可能成为 AML 的新生物标志物。