Suppr超能文献

USF1 在初诊急性髓系白血病中的表达及临床意义。

The Expression and Clinical Significance of USF1 in Newly Diagnosed Acute Myeloid Leukemia.

出版信息

Clin Lab. 2024 Sep 1;70(9). doi: 10.7754/Clin.Lab.2024.240419.

Abstract

BACKGROUND

This study aimed to assess the expression level of upstream stimulator 1 (USF1) in the bone marrow of newly diagnosed acute myeloid leukemia (AML) patients and investigate its clinical and prognostic significance.

METHODS

Bone marrow samples from 60 newly diagnosed AML patients constituted the observation group, while 20 samples from healthy individuals formed the control group. Real-time quantitative PCR (qRT-PCR) was used to measure the USF1 expression in both groups and to analyze its correlation with clinicopathological features and prognosis in AML patients. Kaplan-Meier curves were utilized to assess the impact of USF1 on the overall survival (OS) in AML patients. The prognostic factors of AML were examined by using Cox regression analysis.

RESULTS

A univariate analysis revealed a significantly higher USF1 expression in the AML patients compared to the control group (p < 0.001), with no difference in the clinicopathological features between the low-expression group and the control group. However, there was a significant difference between the high-expression group and the control group (p < 0.01). Moreover, the OS of the high USF1 expression group was notably shorter than of the low USF1 expression group (p < 0.0001). A multivariate analysis identified high USF1 expression and age ≥ 60 years as independent risk factors for a poor AML prognosis.

CONCLUSIONS

High expression of USF1 is linked to a worse prognosis and shorter survival time in AML patients. USF1 may serve as an indicator of prognosis and survival in AML patients and could be a potential target for AML treatment.

摘要

背景

本研究旨在评估新诊断急性髓系白血病(AML)患者骨髓中上游刺激因子 1(USF1)的表达水平,并探讨其临床和预后意义。

方法

观察组纳入 60 例新诊断 AML 患者的骨髓样本,对照组纳入 20 例健康个体的骨髓样本。采用实时定量 PCR(qRT-PCR)测量两组 USF1 的表达水平,并分析其与 AML 患者临床病理特征和预后的关系。Kaplan-Meier 曲线评估 USF1 对 AML 患者总生存期(OS)的影响。采用 Cox 回归分析检验 AML 的预后因素。

结果

单因素分析显示,AML 患者的 USF1 表达明显高于对照组(p<0.001),但低表达组与对照组的临床病理特征无差异。然而,高表达组与对照组之间存在显著差异(p<0.01)。此外,高 USF1 表达组的 OS 明显短于低 USF1 表达组(p<0.0001)。多因素分析确定高 USF1 表达和年龄≥60 岁是 AML 预后不良的独立危险因素。

结论

USF1 的高表达与 AML 患者预后不良和生存时间缩短相关。USF1 可能成为 AML 患者预后和生存的指标,也可能成为 AML 治疗的潜在靶点。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验