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中国重度子痫前期患者胎盘组织中微小RNA的差异表达

Differential expression of microRNAs in the placentae of Chinese patients with severe pre-eclampsia.

作者信息

Hu Yali, Li Pengfei, Hao Sha, Liu Liu, Zhao Junli, Hou Yayi

机构信息

The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing 210008, PR China.

出版信息

Clin Chem Lab Med. 2009;47(8):923-9. doi: 10.1515/CCLM.2009.228.

Abstract

BACKGROUND

The pathogenesis of pre-eclampsia (PE) is incompletely understood. The placenta is considered to play a key role in this disease. Recent research showed that many microRNAs (miRNAs) are expressed in human placenta. Our aim in this study was to determine differential expression of miRNAs in placenta with severe PE, and normal placenta.

METHODS

Differential expression of miRNAs in placenta (four severe PE and a control group of four normal pregnant women) was first screened using microarray analysis. Following this, some differential miRNAs were selected and validated using real-time quantitative reverse transcription-polymerase chain reaction in placenta from women with severe PE (n=24), and a healthy control group (n=26).

RESULTS

We found the following miRNAs were significantly increased in placenta from women with severe PE: miR-16, miR-29b, miR-195, miR-26b, miR-181a, miR-335 and miR-222. Gene ontology analysis of the target genes revealed enrichment for specific biological process categories, i.e., regulation of cellular physiological process including miR-16, miR-29b, miR-195, miR-26b and miR-335, and signal transduction including miR-181a and miR-222.

CONCLUSIONS

These different miRNAs may play an important role in pathogenesis of PE and may become diagnostic markers for PE.

摘要

背景

子痫前期(PE)的发病机制尚未完全明确。胎盘被认为在该疾病中起关键作用。近期研究表明,许多微小RNA(miRNA)在人胎盘中表达。本研究的目的是确定重度PE胎盘与正常胎盘之间miRNA的差异表达。

方法

首先使用微阵列分析筛选胎盘(4例重度PE患者和4例正常孕妇组成的对照组)中miRNA的差异表达。在此之后,选择一些差异miRNA,并在重度PE患者(n = 24)和健康对照组(n = 26)的胎盘中使用实时定量逆转录-聚合酶链反应进行验证。

结果

我们发现以下miRNA在重度PE患者的胎盘中显著增加:miR-16、miR-29b、miR-195、miR-26b、miR-181a、miR-335和miR-222。对靶基因的基因本体分析显示特定生物学过程类别富集,即包括miR-16、miR-29b、miR-195、miR-26b和miR-335的细胞生理过程调节,以及包括miR-181a和miR-222的信号转导。

结论

这些不同的miRNA可能在PE的发病机制中起重要作用,并可能成为PE的诊断标志物。

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