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高原地区重型颅脑损伤患者外周血靶向 miRNA 表达谱的动态变化。

Dynamic changes in peripheral blood-targeted miRNA expression profiles in patients with severe traumatic brain injury at high altitude.

机构信息

Department of Intensive Care Unit, Qinghai Provincial People's Hospital, Xining, 810007, China.

Department of Pathology, Qinghai Provincial People's Hospital, Xining, 810007, China.

出版信息

Mil Med Res. 2019 Apr 30;6(1):12. doi: 10.1186/s40779-019-0203-z.

Abstract

BACKGROUND

The aim of this work is to detect and compare the peripheral blood miRNA expression profiles in patients with severe traumatic brain injury (sTBI) 2, 12, 24, 48, and 72 h after injury at high altitude and to predict the target genes of differential expressed miRNAs.

METHODS

Twenty sTBI patients from high-altitude areas were randomly selected according to the inclusion and exclusion criteria and were divided into five groups: the 2-h group, 12-h group, 24-h group, 48-h group, and 72-h group. Peripheral blood miRNA expression profiles were detected using real-time quantitative PCR (qRT-PCR).

RESULTS

The expression levels of miR-18a, miR-203, miR-146a, miR-149, miR-23b, and miR-let-7b in peripheral blood showed significant differences between the 2-h group and the 12-h group. The expression levels of miR-203, miR-146a, miR-149, miR-23b, and miR-let-7f in peripheral blood were up-regulated in the 24-h group. In the 48-h group, the expression levels of miR-181d, miR-29a, and miR-18b were upregulated. In the 72-h group, the expression levels of miR-203, miR-146a, miR-149, miR-23b, and miR-let-7f changed. The main target genes of the differentiation expressed miRNAs were genes that regulate inflammatory responses, apoptosis, and DNA damage/repair.

CONCLUSIONS

miRNAs may be involved in the pathogenesis of sTBI by dynamically regulating the target genes that regulate inflammatory responses, apoptosis, and DNA damage/repair pathways.

摘要

背景

本研究旨在检测和比较高原地区重型颅脑损伤(sTBI)患者伤后 2、12、24、48 和 72 h 外周血 miRNA 表达谱,并预测差异表达 miRNA 的靶基因。

方法

根据纳入和排除标准,随机选择 20 名来自高原地区的 sTBI 患者,并将其分为五组:2 h 组、12 h 组、24 h 组、48 h 组和 72 h 组。采用实时定量 PCR(qRT-PCR)检测外周血 miRNA 表达谱。

结果

miR-18a、miR-203、miR-146a、miR-149、miR-23b 和 miR-let-7b 在 2 h 组和 12 h 组之间的外周血表达水平存在显著差异。miR-203、miR-146a、miR-149、miR-23b 和 miR-let-7f 在 24 h 组中的表达上调。miR-181d、miR-29a 和 miR-18b 在 48 h 组中表达上调。miR-203、miR-146a、miR-149、miR-23b 和 miR-let-7f 在 72 h 组中表达改变。分化表达 miRNA 的主要靶基因是调节炎症反应、细胞凋亡和 DNA 损伤/修复途径的基因。

结论

miRNA 可能通过动态调节调节炎症反应、细胞凋亡和 DNA 损伤/修复途径的靶基因参与 sTBI 的发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec51/6489315/8325b2c5418a/40779_2019_203_Fig1_HTML.jpg

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