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从分子医学角度探索重度抑郁症中的微小RNA生物标志物

Exploring miRNA Biomarkers in Major Depressive Disorder: A Molecular Medicine Perspective.

作者信息

Prodan-Bărbulescu Cătălin, Ghenciu Laura Andreea, Şeclăman Edward, Bujor Georgeta Cristiana, Enătescu Virgil, Danila Alexandra-Ioana, Dăescu Ecaterina, Rosu Luminioara Maria, Faur Ionuţ Flaviu, Tuţac Paul, Varga Norberth-Istvan, Sonia Tanasescu, Duță Ciprian

机构信息

Faculty of Medicine, "Victor Babeş" University of Medicine and Pharmacy Timisoara, 2nd Eftimie Murgu Square, 300041 Timisoara, Romania.

Department I-Discipline of Anatomy and Embryology, Faculty of Medicine, "Victor Babeş" University of Medicine and Pharmacy Timisoara, 2nd Eftimie Murgu Square, 300041 Timișoara, Romania.

出版信息

Curr Issues Mol Biol. 2024 Sep 27;46(10):10846-10853. doi: 10.3390/cimb46100644.

DOI:10.3390/cimb46100644
PMID:39451524
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11506240/
Abstract

Major depressive disorder (MDD) is a complex mental health condition with a multifaceted and incompletely elucidated pathophysiology. MicroRNAs (miRNAs) have emerged as potential biomarkers due to their role in gene regulation and the observed dysregulation in MDD. The aim of this study is to detect the presence of specific molecular diagnostic biomarkers in major depressive disorder. This cross-sectional study analyzed plasma miRNA expression in ten MDD patients and eight healthy controls using real-time PCR. Differentially expressed miRNAs were identified using independent -tests, and their diagnostic potential was assessed with ROC curve analysis. Fifteen miRNAs exhibited significant dysregulation in MDD patients. Notably, hsa-miR-29c-3p, hsa-miR-376a-3p, hsa-miR-532-5p, and hsa-miR-339-5p showed excellent discriminatory power (AUC > 0.8). This study identifies differentially expressed plasma miRNAs in MDD, suggesting their potential for improved diagnosis and personalized treatment. However, further validation in larger cohorts and investigation into their functional roles are warranted.

摘要

重度抑郁症(MDD)是一种复杂的心理健康状况,其病理生理学多方面且尚未完全阐明。微小RNA(miRNA)因其在基因调控中的作用以及在MDD中观察到的失调现象而成为潜在的生物标志物。本研究的目的是检测重度抑郁症中特定分子诊断生物标志物的存在。这项横断面研究使用实时聚合酶链反应分析了10名MDD患者和8名健康对照者血浆中的miRNA表达。使用独立样本t检验鉴定差异表达的miRNA,并通过ROC曲线分析评估其诊断潜力。15种miRNA在MDD患者中表现出显著失调。值得注意的是,hsa-miR-29c-3p、hsa-miR-376a-3p、hsa-miR-532-5p和hsa-miR-339-5p显示出优异的鉴别能力(曲线下面积>0.8)。本研究鉴定了MDD中差异表达的血浆miRNA,表明它们在改善诊断和个性化治疗方面的潜力。然而,需要在更大的队列中进一步验证并研究它们的功能作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0ba/11506240/4796ffbabe7f/cimb-46-00644-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0ba/11506240/4796ffbabe7f/cimb-46-00644-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0ba/11506240/4796ffbabe7f/cimb-46-00644-g001.jpg

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本文引用的文献

1
Evaluating the Connection between MicroRNAs and Long Non-Coding RNAs for the Establishment of the Major Depressive Disorder Diagnosis.评估微小RNA与长链非编码RNA之间的联系以建立重度抑郁症诊断
Biomedicines. 2024 Feb 25;12(3):516. doi: 10.3390/biomedicines12030516.
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Major depressive disorder.重度抑郁症。
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Circulating hsa-let-7e-5p and hsa-miR-125a-5p as Possible Biomarkers in the Diagnosis of Major Depression and Bipolar Disorders.循环 hsa-let-7e-5p 和 hsa-miR-125a-5p 作为诊断重度抑郁症和双相情感障碍的潜在生物标志物。
Dis Markers. 2022 Feb 7;2022:3004338. doi: 10.1155/2022/3004338. eCollection 2022.
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miR-376a-3p and miR-376b-3p overexpression in Hutchinson-Gilford progeria fibroblasts inhibits cell proliferation and induces premature senescence.在早老症成纤维细胞中过表达miR-376a-3p和miR-376b-3p可抑制细胞增殖并诱导早衰。
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Uncovering the Roles of MicroRNAs in Major Depressive Disorder: From Candidate Diagnostic Biomarkers to Treatment Response Indicators.揭示微小RNA在重度抑郁症中的作用:从候选诊断生物标志物到治疗反应指标
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Bioinformatics analysis of a TF-miRNA-lncRNA regulatory network in major depressive disorder.生物信息学分析在重度抑郁症中 TF-miRNA-lncRNA 调控网络
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MiRNA-532-5p Regulates CUMS-Induced Depression-Like Behaviors and Modulates LPS-Induced Proinflammatory Cytokine Signaling by Targeting STAT3.微小RNA-532-5p通过靶向信号转导和转录激活因子3调控慢性不可预知温和应激诱导的抑郁样行为并调节脂多糖诱导的促炎细胞因子信号传导。
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MicroRNA‑29c‑3p acts as a tumor suppressor gene and inhibits tumor progression in hepatocellular carcinoma by targeting TRIM31.微小RNA-29c-3p作为一种肿瘤抑制基因,通过靶向TRIM31抑制肝细胞癌的肿瘤进展。
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