LncRNA SNHG14是抑郁症患者的生物标志物,并通过MiR-200a-3p调控抑郁样行为

IF 1.7 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Tohoku Journal of Experimental Medicine Pub Date : 2024-05-30 Epub Date: 2024-03-01 DOI:10.1620/tjem.2024.J007
HongLi Wang, SiWen Deng, Juan Bi
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引用次数: 0

摘要

抑郁症已成为一种主要的精神疾病,在全球范围内受到特别关注。确定抑郁症诊断和严重程度的特异性生物标志物将有利于抑郁症的临床治疗。本研究关注lncRNA SNHG14在抑郁症中的意义,并研究其对抑郁样行为的影响,旨在探索抑郁症发生和发展的潜在生物标志物。本研究纳入了147名抑郁症患者和98名健康人。所有参与者的血清 SNHG14 均通过 PCR 进行分析,其诊断价值通过接收器运算特征曲线(ROC)分析进行评估。通过慢性社会挫败应激(CSDS)诱导抑郁样行为,并通过蔗糖偏好、强迫游泳和开阔场地测试进行评估。与健康人相比,SNHG14在抑郁症患者中明显上调,它能以相对较高的效率区分抑郁症患者。病情严重的抑郁症患者血清中SNHG14水平更高,SNHG14与PHQ9评分呈显著正相关。在 CSDS 小鼠中,观察到 SNHG14 增加,而 miR-200a-3p 减少。沉默SNHG14和过表达miR-200a-3p能缓解CSDS引起的蔗糖偏好降低、游泳不动时间延长、站立时间缩短和行走距离缩短。敲除SNHG14可促进miR-200a-3p的表达,而沉默miR-200a-3p可逆转SNHG14对抑郁样行为的保护作用。SNHG14可作为抑郁症发生和严重程度的生物标志物。沉默SNHG14可通过调节miR-200a-3p缓解抑郁样行为。
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LncRNA SNHG14 Served as a Biomarker of Depression Disorder Patients and Regulated Depression-Like Behaviors via MiR-200a-3p.

Depression disorder has become a major mental disease and has attracted special attention globally. Identifying specific biomarkers for the diagnosis and severity of depression disorder would benefit its clinical management. This study focused on the significance of lncRNA SNHG14 in depression disorder and investigated its effect on depression-like behaviors, aiming to explore a potential biomarker for depression disorder occurrence and development. This study included 147 patients with depression disorder and 98 healthy individuals. The serum SNHG14 in all participants was analyzed by PCR, and its diagnostic value was evaluated by receiver operatorating characteristic curve (ROC) analysis. The depression-like behaviors were induced via chronic social defeat stress (CSDS) and evaluated by sucrose preference, forced swimming, and open field tests. SNHG14 was significantly upregulated in depression disorder patients relative to healthy individuals, which discriminated depression disorder patients with a relatively high efficiency. Depression disorder patients with severe conditions showed higher serum SNHG14 levels, and a significantly positive correlation of SNHG14 with PHQ9 score was demonstrated. In CSDS mice, increasing SNHG14 and decreasing miR-200a-3p were observed. Silencing SNHG14 and overexpressing miR-200a-3p could alleviate reduced sucrose preference, increased swimming immobility time, decreased standing times, and decreased traveling distance induced by CSDS. The knockdown of SNHG14 promoted the expression of miR-200a-3p, and silencing miR-200a-3p could reverse the protective effect of SNHG14 silencing on depression-like behaviors. SNHG14 served as a biomarker for the occurrence and severity of depression disorder. Silencing SNHG14could alleviate depression-like behaviors via modulating miR-200a-3p.

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