[急性白血病患者核极小 RNA SNORA63 的异常表达及其临床意义]。

Yan-Quan Liu, Shao-Peng Chen, Yue Yin, Jian-Zhen Shen, Min-Juan Zeng
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引用次数: 0

摘要

目的研究急性白血病(AL)患者骨髓中小核RNA(snoRNA)SNORA63的表达水平及其在AL患者临床诊断、治疗和预后中的意义:收集广东医科大学附属医院2018年3月至2021年12月新确诊的53例AL患者和29例健康人的骨髓标本。采用定量实时聚合酶链反应(qRT-PCR)检测两组骨髓单核细胞中SNORA63的相对表达水平。以SNORA63在AL患者中的中位表达水平为界限值,将患者分为SNORA63高表达组和低表达组,并分析讨论SNORA63的表达水平与AL患者的临床特征、临床指标及预后的关系:结果:SNORA63在AL患者中的相对表达水平明显低于健康对照组[0.3018 (0.0244-1.2792) vs 1.0882 (0.2797-1.9889)](P < 0.01)。初次治疗后未缓解的AL患者的SNORA63表达水平明显低于健康对照组和完全缓解(CR)患者(P<0.01),而AML组和ALL组之间的SNORA63表达水平无统计学差异(P>0.05)。SNORA63的异常低表达与AL患者的发热、出血、预后不良、疗效、血小板(PLT)、乳酸脱氢酶(LDH)、白蛋白(ALB)和分子生物学异常密切相关(P < 0.05),但与性别、年龄、AL亚型、苍白、乏力、髓外浸润、白细胞计数(WBC)、血红蛋白(HGB)、C反应蛋白(CRP)、降钙素原(PCT)、纤维蛋白原(FIB)或染色体核型无明显相关性(P >0.05)。同时,SNORA63高表达组AL患者的总生存期(OS)和无事件生存期(EFS)明显高于SNORA63低表达组(P<0.05)。单变量Cox回归分析显示,SNORA63、分子生物学异常、发热、PLT和LDH是影响AL患者OS和EFS的因素(P<0.05)。多变量Cox回归分析表明,发热、分子生物学异常和LDH是AL患者OS和EFS的独立相关因素(P<0.05):结论:SNORA63在AL患者中明显下表达,该分子标志物对AL患者的病情监测和预后评估具有重要的临床价值。
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[Aberrant Expression of Small Nucleolar RNA SNORA63 and Its Clinical Significance in Patients with Acute Leukemia].

Objective: To investigate the expression level of small nucleolar RNA (snoRNA) SNORA63 in bone marrow of patients with acute leukemia (AL) and its significance in the clinical diagnosis, treatment and prognosis of AL patients.

Methods: Bone marrow samples of 53 newly diagnosed AL patients and 29 healthy subjects in the Affiliated Hospital of Guangdong Medical University from March 2018 to December 2021 were collected. Quantitative real-time polymerase chain reaction (qRT-PCR) was used to detect the relative expression level of SNORA63 in bone marrow mononuclear cells of the two groups. The median expression level of SNORA63 in AL patients was used as the boundary value to divide the patients into SNORA63 high and low expression groups, and the relationship between the expression level of SNORA63 and the clinical characteristics, clinical indicators and prognosis of AL patients was analyzed and discussed.

Results: The relative expression level of SNORA63 in AL patients was significantly lower than that in healthy control group [0.3018 (0.0244-1.2792) vs 1.0882 (0.2797-1.9889)] (P < 0.01). The expression level of SNORA63 in AL patients without remission after initial treatment was significantly lower than that in healthy controls and the patients who received complete remission (CR) (P < 0.01), while there was no statistical difference in the expression level of SNORA63 between AML and ALL groups (P >0.05). The abnormal low expression of SNORA63 was closely related to fever, hemorrage, poor prognosis, efficacy, platelets (PLT), lactate dehydrogenase (LDH), albumin (ALB), and molecular biological abnormalities of AL patients (P < 0.05), but not significantly correlated with sex, age, AL subtype, pallor, fatigue, extramedullary infiltration, white blood cell count (WBC), hemoglobin (HGB), C-reactive protein (CRP), procalcitonin (PCT), fibrinogen (FIB) or chromosome karyotype (P >0.05). Meanwhile, overall survival (OS) and event-free survival (EFS) of AL patients in SNORA63 high-expression group were significantly higher than those in SNORA63 low-expression group (P < 0.05). Univariate Cox regression analysis showed that SNORA63, molecular biological abnormalities, fever, PLT and LDH were the factors influencing OS and EFS in AL patients (P < 0.05). Multivariate Cox regression analysis indicated that fever, molecular biological abnormalities and LDH were independent factors associated with OS and EFS in AL patients (P < 0.05).

Conclusion: SNORA63 is significantly down-expressed in AL patients, which is a molecular marker of great clinical value for disease monitoring and prognosis evaluation in AL 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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