Altered Expression of GABPB1-IT1 and SLC9A3-AS1 Long Non-Coding RNAs in Recurrent Implantation Failure.

Q2 Medicine
Majid Zaki-Dizaji, Amir Ebrahimi, Behnoosh Jamshidi, Seyed Mohammad Hossein Nemati, Reza Saeedinia, Zohreh Heidary
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引用次数: 0

Abstract

Background: Recurrent implantation failure (RIF) impairs assisted reproductive technology (ART) success, though its mechanisms remain unclear. Studies have implicated altered miRNA expression in the plasma and endometrium of patients with RIF. In this study, long non-coding RNA (lncRNA) expression in plasma was investigated, using RIF-specific lncRNA-miRNA-mRNA network as guide.

Methods: This study included 30 women with RIF and 30 age-matched controls (Not RIF). RIF miRNA RNA-seq data (GSE108966) was downloaded from the Gene Expression Omnibus (GEO) database and used to identify differentially expressed miRNAs. Next, miRNet 2.0 database was used to integrate the latest miRNA-mRNA interactions; also, the linkages between lncRNA and miRNA were identified and the networks created. Plasma samples were collected from participants during the implantation window. Cell-free RNA was extracted from 500 μl of plasma using the TRIzol method, and statistical analyses were performed using Prism version 8.0.

Results: Based on a lncRNA-miRNA-mRNA network analysis, two lncRNAs, including GABPB1-IT1 and SLC9A3-AS1, were selected for expression analysis in plasma. Notably, GABPB1-IT1 and SLC9A3-AS1 were significantly downregulated in RIF samples compared to controls.

Conclusion: Our findings show that GABPB1-IT1 and SLC9A3-AS1 are significantly downregulated in the plasma of women with recurrent implantation failure. These findings suggest their potential involvement in RIF and warrant further studies to elucidate their biological functions and evaluate their utility as non-invasive biomarkers.

GABPB1-IT1和SLC9A3-AS1长链非编码rna在复发性植入失败中的表达改变
背景:反复植入失败(RIF)影响辅助生殖技术(ART)的成功,尽管其机制尚不清楚。研究表明RIF患者血浆和子宫内膜中miRNA表达发生改变。本研究以rif特异性lncRNA- mirna - mrna网络为指导,研究长链非编码RNA (long non-coding RNA, lncRNA)在血浆中的表达。方法:本研究包括30名患有RIF的女性和30名年龄匹配的对照组(非RIF)。从Gene Expression Omnibus (GEO)数据库下载RIF miRNA RNA-seq数据(GSE108966),用于鉴定差异表达的miRNA。接下来,使用miRNet 2.0数据库整合最新的miRNA-mRNA相互作用;此外,lncRNA和miRNA之间的联系被确定并创建了网络。在植入窗口期间从参与者收集血浆样本。采用TRIzol法从500 μl血浆中提取无细胞RNA,使用Prism version 8.0进行统计学分析。结果:基于lncRNA-miRNA-mRNA网络分析,选择GABPB1-IT1和SLC9A3-AS1两个lncrna在血浆中的表达分析。值得注意的是,与对照组相比,GABPB1-IT1和SLC9A3-AS1在RIF样本中显著下调。结论:反复植入失败患者血浆中GABPB1-IT1和SLC9A3-AS1明显下调。这些发现表明它们可能参与RIF,需要进一步的研究来阐明它们的生物学功能并评估它们作为非侵入性生物标志物的效用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Reproduction and Infertility
Journal of Reproduction and Infertility Medicine-Reproductive Medicine
CiteScore
2.70
自引率
0.00%
发文量
44
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