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重度子痫前期患者胎盘mir-155-5p和长链非编码RNA sONE表达的评估

Evaluation of Placental mir-155-5p and Long Non-coding RNA sONE Expression in Patients with Severe Pre-eclampsia.

作者信息

Azizi Faezeh, Saleh Gargari Soraya, Asadi Shahmirzadi Sedigheh, Dodange Fatemeh, Amiri Vahid, Mirfakhraie Reza, Omrani Mir Davood

机构信息

Department of Medical Genetics, Faculty of Medicine, ShahidBeheshtiUniversity of Medical Sciences,Tehran, Iran.

Feto-Maternal Unit, ShohadayeTajrish Hospital, ShahidBeheshti, University of Medical Sciences, Tehran, Iran.

出版信息

Int J Mol Cell Med. 2017 Winter;6(1):22-30. Epub 2017 Jan 17.

PMID:28868266
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5568189/
Abstract

It has been well documented that preeclampsia (PE) has a common etiological background, but little is known about its linkage at the molecular level.Non- coding RNAs are critical posttranscriptional regulators ofgene expression. This study was performed to determine whether PE is associated with alterations in placental non-coding RNAs expression. MicroRNA (miR)-155-5p and long non-coding RNA () expression, in placentas collected sequentially from 59 patients with PE and 40 normotensive pregnancies were measured using real-time PCR.The relationship between miR-155-5p and expressions was analyzed statistically. miR-155-5p expression was increased (fold change =1.6, P=0.04), while lncsONE expression was not significantly changed (fold change =1.1, P=0.68), in placentas from patients compared with control group.miR-155-5p was upregulated in placentas from patients with PE and may have influenced expression. These findings indicate that miRNA-155-5p may be involved in PE pathogenesis and could be a potential biomarker for this disease.

摘要

已有充分文献记载,子痫前期(PE)具有共同的病因背景,但在分子水平上其关联尚不清楚。非编码RNA是基因表达的关键转录后调节因子。本研究旨在确定PE是否与胎盘非编码RNA表达的改变有关。使用实时PCR检测了从59例PE患者和40例血压正常的孕妇中依次收集的胎盘组织中微小RNA(miR)-155-5p和长链非编码RNA(lncRNA)的表达。对miR-155-5p和lncRNA的表达关系进行了统计学分析。与对照组相比,患者胎盘组织中miR-155-5p表达增加(倍数变化=1.6,P=0.04),而lncRNA lncSONE表达无明显变化(倍数变化=1.1,P=0.68)。PE患者胎盘中miR-155-5p上调,可能影响了lncSONE的表达。这些发现表明,miRNA-155-5p可能参与PE的发病机制,可能是该疾病的潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21d3/5568189/b0687d43656c/ijmcm-6-022-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21d3/5568189/e9f1f94fa6fa/ijmcm-6-022-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21d3/5568189/6a4b25f8f47b/ijmcm-6-022-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21d3/5568189/b0687d43656c/ijmcm-6-022-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21d3/5568189/e9f1f94fa6fa/ijmcm-6-022-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21d3/5568189/6a4b25f8f47b/ijmcm-6-022-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21d3/5568189/b0687d43656c/ijmcm-6-022-g003.jpg

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