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lncRNA BLACAT1 在急性髓系白血病患者外周血中的表达及诊断价值。

Expression and Diagnostic Value of lncRNA BLACAT1 in Peripheral Blood of Patients with Acute Myeloid Leukemia.

出版信息

Clin Lab. 2020 Apr 1;66(4). doi: 10.7754/Clin.Lab.2019.190802.

Abstract

BACKGROUND

The current study aims to investigate the expression of lncRNA BLACAT1 in patients with acute myeloid leukemia (AML) and to analyze its correlation with clinical prognosis.

METHODS

Peripheral blood samples were collected from 68 AML patients, including 48 patients with acute myeloid leukemia (AML), 20 patients with complete response (CR), and 30 patients with iron deficiency anemia (control group). LncRNA BLACAT1 was detected by real-time fluorescence quantitative PCR (qRT-PCR). The expression of BLACAT1 and its relationship with clinicopathological characteristics and prognosis were analyzed.

RESULTS

The expression of lncRNA BLACAT1 in AML patients was significantly higher than that in complete remission patients and iron deficiency anemia patients, but the expression of lncRNA BLACAT1 in AML-CR group and control group had no significant difference. Further study showed that the expression of lncRNA BLACAT1 was correlated with the National Comprehensive Cancer Network (NCCN) risk classification, the amount of platelet and bone marrow primordial cells (%), and survival status of patients. The median overall survival time of patients with high expression of lncRNA BLACAT1 was significantly shorter than those with low expression of lncRNA BLACAT1 (p < 0.05).

CONCLUSIONS

LncRNA BLACAT1 was involved in regulating the occurrence and development of AML and can be used as a potential prognostic marker and therapeutic target for AML patients.

摘要

背景

本研究旨在探讨长链非编码 RNA BLACAT1 在急性髓系白血病(AML)患者中的表达,并分析其与临床预后的相关性。

方法

收集 68 例 AML 患者的外周血样本,其中急性髓系白血病(AML)患者 48 例,完全缓解(CR)患者 20 例,缺铁性贫血患者 30 例。采用实时荧光定量 PCR(qRT-PCR)检测 lncRNA BLACAT1 的表达。分析 BLACAT1 的表达及其与临床病理特征和预后的关系。

结果

AML 患者中 lncRNA BLACAT1 的表达明显高于完全缓解患者和缺铁性贫血患者,但 AML-CR 组和对照组 lncRNA BLACAT1 的表达无明显差异。进一步研究表明,lncRNA BLACAT1 的表达与美国国家综合癌症网络(NCCN)风险分类、血小板计数和骨髓原始细胞(%)以及患者的生存状况有关。lncRNA BLACAT1 高表达患者的中位总生存时间明显短于 lncRNA BLACAT1 低表达患者(p<0.05)。

结论

lncRNA BLACAT1 参与调节 AML 的发生和发展,可作为 AML 患者潜在的预后标志物和治疗靶点。

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