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Integrated analysis of lncRNA and mRNA expression profiles in patients with unexplained recurrent spontaneous abortion

生物 免疫系统 信使核糖核酸 免疫学 发病机制 基因 外周血 CD14型 基因表达 生物信息学 遗传学
作者
Xiaoli Zhu,Meng‐Xuan Du,Heng Gu,Ruishan Wu,Mengge Gao,Hang Xu,Jia Tang,Mingzhen Li,Xiaohua Liu,Xingming Zhong
出处
期刊:American Journal of Reproductive Immunology [Wiley]
卷期号:89 (6): e13691-e13691 被引量:11
标识
DOI:10.1111/aji.13691
摘要

Abstract Problem Unexplained recurrent spontaneous abortion (URSA) is one of the most frustrating and confounding conditions in reproductive medicine, and its exact pathogenesis has not been clearly established. Method of study In this study, we used RNA sequencing to characterize the mRNA and lncRNA expression profiles in peripheral blood. Thereafter, enrichment analysis was performed to determine the functions of the differentially expressed genes, and Cytoscape was used to construct lncRNA‐mRNA interaction networks. Results Our results showed that the peripheral blood of patients with URSA has distinct mRNA and lncRNA expression profiles, with a total of 359 mRNAs and 683 lncRNAs being differentially expressed. Moreover, the top hub genes, including IGF1, PPARG, CCL3, RETN, SERPINE1, HESX1 , and PRL , were identified and further validated using real‐time quantitative PCR. Furthermore, we demonstrated a lncRNA‐mRNA interaction network that achieved 12 key lncRNAs and their targeted mRNAs are involved in systemic lupus erythematosus, allograft rejection, and complement and coagulation cascades. Finally, the correlation between immune cell subtypes and IGF1 expression was evaluated; a negative correlation was observed with the proportion of natural killer cells, which increased significantly in URSA. Conclusion We identified seven top hub genes, constructed a lncRNA‐related network and suggested that IGF1 plays a key role in regulating maternal immune response by affecting NK and T cells’ function, which helps to identify the pathogenesis of URSA.
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