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miR-17~92 簇在慢性淋巴细胞白血病中的预后价值。

Prognostic Value of the miR-17~92 Cluster in Chronic Lymphocytic Leukemia.

机构信息

Department of Haematooncology and Bone Marrow Transplantation, Medical University of Lublin, 20-080 Lublin, Poland.

Department of Clinical Immunology, Medical University of Lublin, 20-093 Lublin, Poland.

出版信息

Int J Mol Sci. 2023 Jan 15;24(2):1705. doi: 10.3390/ijms24021705.

Abstract

The aim of this study was to investigate the expression of miR-17∼92 cluster members in chronic lymphocytic leukemia (CLL) patients. Six microRNAs (miRNAs)-miR-17, miR-18a, miR-19a, miR-19b-1, miR-20a, and miR-92a-1-very poorly characterized in CLL patients, were chosen for the study to consider their possible role as cancer biomarkers. It is currently unclear to which extent miR-1792 expression is related to other routinely measured CLL markers, and whether the findings can be of any clinical significance. To achieve this goal, we report the expression levels of these miRNAs detected by RT-qPCR in purified CD19+ B lymphocytes of 107 CLL patients and correlate them with existing clinical data. The study provides new evidence regarding the heterogeneity of miR-1792 cluster members' expression in CLL patients. Higher miR-17-5p expression was associated with unfavorable prognostic factors (i.e., 17p and 11q deletions, CD38 and ZAP-70 expression). On the other hand, miR-19a, miR-20a, and miR-92a-1 negatively correlated with these adverse factors. The presence of del(13q) as a sole aberration was associated with a significantly lower miR-17-5p as well as higher miR-19a-3p and miR-92a-1-5p expression compared to patients carrying unfavorable genetic aberrations. Particularly, miR-20a could be considered an independent favorable prognostic factor. In a multivariate analysis, high miR-20a expression remained an independent marker predicting long TTT (time to treatment) for CLL patients.

摘要

本研究旨在探讨慢性淋巴细胞白血病(CLL)患者中 miR-17∼92 簇成员的表达情况。选择了六个在 CLL 患者中特征较差的 microRNAs(miRNAs)-miR-17、miR-18a、miR-19a、miR-19b-1、miR-20a 和 miR-92a-1,以考虑它们作为癌症生物标志物的可能作用。miR-1792 的表达与其他常规测量的 CLL 标志物的关系,以及这些发现是否具有任何临床意义,目前尚不清楚。为了实现这一目标,我们报告了通过 RT-qPCR 在 107 例 CLL 患者纯化的 CD19+B 淋巴细胞中检测到的这些 miRNA 的表达水平,并将其与现有临床数据相关联。该研究提供了有关 miR-1792 簇成员在 CLL 患者中表达异质性的新证据。较高的 miR-17-5p 表达与不良预后因素(即 17p 和 11q 缺失、CD38 和 ZAP-70 表达)相关。另一方面,miR-19a、miR-20a 和 miR-92a-1 与这些不良因素呈负相关。与携带不良遗传异常的患者相比,单纯 del(13q) 作为唯一异常与 miR-17-5p 显著降低以及 miR-19a-3p 和 miR-92a-1-5p 表达升高相关。特别是,miR-20a 可被视为独立的有利预后因素。在多变量分析中,高 miR-20a 表达仍然是预测 CLL 患者 TTT(治疗时间)的独立标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1d9/9866777/95ea2e60df99/ijms-24-01705-g001.jpg

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