[急性髓性白血病患者中 lncRNA UCA1 的表达及其临床意义]。

Q4 Medicine
Xue Bai, Yan-Ping Wu, Zhong-Yu Li, Xiao-Feng Chen, Meng Wang, Jia-Jia Li
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引用次数: 0

摘要

目的研究急性髓性白血病(AML)患者骨髓中尿路癌胚抗原1(lncRNA UCA1)的表达水平,并探讨lncRNA UCA1表达水平在AML患者中的临床意义:方法:采集50例AML患者骨髓样本作为实验组,20例缺铁性贫血(IDA)患者骨髓样本作为对照组。收集 AML 患者的相关临床病理特征。采用实时定量 PCR(qRT-PCR)技术检测实验组和对照组中 lncRNA UCA1 的表达水平,分析 lncRNA UCA1 表达与 AML 患者临床病理特征和预后的关系。采用Kaplan-Meier曲线分析lncRNA UCA1对AML患者总生存期(OS)的影响;采用Cox回归模型分析影响AML患者预后的因素:与对照组相比,lncRNA UCA1在AML患者中的表达水平明显升高(P < 0.001);lncRNA UCA1高表达组患者血红蛋白低于90 g/L的比例明显高于lncRNA UCA1低表达组(P =0.004);lncRNA UCA1在M1、M2和M4亚型中表达水平较高,而在M0和M5亚型中表达水平较低,差异有统计学意义(P =0.009)。UCA1高表达组患者与UCA1低表达组患者在性别、年龄、白细胞(WBC)计数、血小板(PLT)计数、骨髓细胞数、化疗方案及疗效、核型、基因突变、预后风险分层等方面均无明显差异(均P>0.05)。lncRNA UCA1高表达组患者的OS明显短于lncRNA UCA1低表达组患者(P =0.0229):结论:lncRNA UCA1的表达水平在AML患者中明显上调。lncRNA UCA1的高表达与不良临床病理特征和不良预后相关。因此,lncRNA UCA1可作为AML患者的预后指标和潜在治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Expression of lncRNA UCA1 in Acute Myeloid Leukemia Patients and Its Clinical Significance].

Objective: To investigate the expression level of urothelial carcinoembryonic antigen 1 (lncRNA UCA1) in the bone marrow of acute myeloid leukemia (AML) patients, and to explore the clinical significance of lncRNA UCA1 expression level in AML patients.

Methods: Bone marrow samples of 50 AML patients were collected as experimental group, and bone marrow samples of 20 iron deficiency anemia (IDA) patients were collected as control group. The relevant clinicopathological characteristics of AML patients were collected. Real-time quantitative PCR (qRT-PCR) was used to detect the expression level of lncRNA UCA1 in the experimental and control groups, and the relationships between lncRNA UCA1 expression and clinical pathological characteristics and prognosis in AML patients were analyzed. Kaplan-Meier curves were used to analyze the effect of lncRNA UCA1 on the overall survival (OS) of AML patients; And Cox regression model was used to analyze the factors affecting the prognosis of AML patients.

Results: Compared with the control group, the expression level of lncRNA UCA1 was significantly elevated in patients with AML (P < 0.001); The proportion of patients with hemoglobin lower than 90 g/L in lncRNA UCA1 high expression group was significantly higher than that in lncRNA UCA1 low expression group (P =0.004); The expression level of lncRNA UCA1 was higher in M1, M2, and M4 subtypes, while it was lower in M0 and M5 subtypes, and the difference was statistically significant (P =0.009). There were no significant difference in sex, age, white blood cell (WBC) count, platelet (PLT) count, bone marrow blasts , chemotherapy regimen and efficacy, karyotype, gene mutation, and prognostic risk stratification between patients in UCA1 high expression group and those in UCA1 low expression group (all P > 0.05). The OS of patients with high expression of lncRNA UCA1 was significantly shorter than that of patients with low expression of lncRNA UCA1 (P =0.0229).

Conclusion: The expression level of lncRNA UCA1 is significantly upregulated in AML patients. High expression of lncRNA UCA1 is associated with poor clinicopathological features and poor prognosis. Therefore, lncRNA UCA1 can be used as a prognostic indicator and a potential therapeutic target for AML patients.

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中国实验血液学杂志
中国实验血液学杂志 Medicine-Medicine (all)
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0.40
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