Yang Lan, Zhou Jing-Dong, Zhang Ting-Juan, Ma Ji-Chun, Xiao Gao-Fei, Chen Qin, Deng Zhao-Qun, Lin Jiang, Qian Jun, Yao Dong-Ming
Laboratory Center, Affiliated People's Hospital of Jiangsu University, Zhenjiang, Jiangsu, People's Republic of China,
The Key Laboratory of Precision Diagnosis and Treatment of Zhenjiang City, Zhenjiang, Jiangsu, People's Republic of China,
Cancer Manag Res. 2018 Oct 29;10:4999-5007. doi: 10.2147/CMAR.S180150. eCollection 2018.
Abundant studies have shown that lncRNA plays an oncogenic role in human solid tumors. Although abnormal expression of has been well investigated in solid tumors, it was rarely studied in hematologic diseases. Hence, the aim of this study was to determine the expression level and its clinical significance in patients with acute myeloid leukemia (AML).
For detecting the expression level of in 119 AML patients and 26 controls, real-time quantitative PCR was used in this study. The prognostic values were evaluated by using Kaplan-Meier analysis, Cox regression analyses, and logistic regression analysis.
was significantly overexpressed in AML and might be a promising biomarker which could distinguish AML from normal samples (<0.001). Patients with high expression of ( ) were older and showed higher bone marrow blasts than patients in group (=0.029 and 0.032, respectively). Significant differences between these groups were also detected regarding risk group and karyotype finding (=0.009 and 0.041, respectively). Importantly, patients presented a significant lower complete remission rate compared to patients (<0.001). Furthermore, Kaplan-Meier analysis showed that patients had shorter overall survival compared to patients observing the whole AML cohort, and also in the non-M3 group of patients (<0.001 and =0.005, respectively). Multivariate analysis of Cox and logistic regression analysis confirmed that high expression was an independent unfavorable risk factor for overall survival and complete remission in both observed patient groups.
These results revealed that was overexpressed in AML, and that higher expression was associated with poor clinical outcome. Our study therefore suggests that expression is a promising biomarker for prognostic prediction for AML.
大量研究表明,长链非编码RNA(lncRNA)在人类实体瘤中发挥致癌作用。尽管lncRNA的异常表达在实体瘤中已得到充分研究,但在血液系统疾病中却鲜有研究。因此,本研究旨在确定急性髓系白血病(AML)患者中lncRNA的表达水平及其临床意义。
本研究采用实时定量PCR检测119例AML患者和26例对照中lncRNA的表达水平。通过Kaplan-Meier分析、Cox回归分析和逻辑回归分析评估预后价值。
lncRNA在AML中显著过表达,可能是一种有前景的生物标志物,可将AML与正常样本区分开来(<0.001)。lncRNA高表达( )的患者年龄较大,骨髓原始细胞比例高于低表达组患者(分别为=0.029和0.032)。在风险组和核型结果方面,这些组之间也存在显著差异(分别为=0.009和0.041)。重要的是,高表达组患者的完全缓解率明显低于低表达组患者(<0.001)。此外,Kaplan-Meier分析显示,在整个AML队列以及非M3组患者中,高表达组患者与低表达组患者相比总生存期较短(分别为<0.001和=0.005)。Cox多因素分析和逻辑回归分析证实,lncRNA高表达是两个观察患者组总生存期和完全缓解的独立不良风险因素。
这些结果表明lncRNA在AML中过表达,且较高的lncRNA表达与不良临床结局相关。因此,我们的研究表明lncRNA表达是AML预后预测的一个有前景的生物标志物。