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微小RNA和外泌体微小RNA可能是妊娠期糖尿病研究的潜在靶点。

MicroRNAs and Exosomal microRNAs May Be Possible Targets to Investigate in Gestational Diabetes Mellitus.

作者信息

Yang Xiyao, Wu Na

机构信息

Department of Endocrinology, Shengjing Hospital of China Medical University, Shenyang, People's Republic of China.

Clinical Skills Practice Teaching Center, Shengjing Hospital of China Medical University, Shenyang, People's Republic of China.

出版信息

Diabetes Metab Syndr Obes. 2022 Feb 3;15:321-330. doi: 10.2147/DMSO.S330323. eCollection 2022.

Abstract

Gestational diabetes mellitus (GDM) is defined as glucose intolerance that occurs during the second or third trimester of pregnancy. As the incidence of GDM rises, so does the risk of maternal and fetal complications with short- and long-term consequences. As a result, early diagnosis and treatment of this condition are important to avoiding adverse pregnancy outcomes. Exosomes are tiny vesicles secreted by living cells which contain a variety of bioactive substances. They are released by cells to facilitate cell-to-cell communication and regulate a variety of biological processes such as cellular immune response, inflammatory response, and apoptosis, among others. Many studies have recently confirmed that changes in the expression and secretion of exosomal miRNAs can be used as novel markers for the diagnosis, prognosis, and treatment of GDM. In this review, we summarized the various roles of exosomal miRNAs and circulating miRNAs in GDM. We found that the changes in the expression of certain miRNAs could be used to diagnosing GDM. Exosomal miRNAs target metabolic pathways, resulting in insulin resistance. We also highlighted the potential for miRNAs and exosomal miRNAs to be used as biomarkers for diagnosis or therapeutic agents.

摘要

妊娠期糖尿病(GDM)被定义为在妊娠中期或晚期出现的葡萄糖不耐受。随着GDM发病率的上升,母婴并发症的风险也随之增加,且会产生短期和长期后果。因此,早期诊断和治疗这种疾病对于避免不良妊娠结局很重要。外泌体是活细胞分泌的微小囊泡,其中含有多种生物活性物质。它们由细胞释放以促进细胞间通讯,并调节多种生物过程,如细胞免疫反应、炎症反应和细胞凋亡等。最近许多研究证实,外泌体微小RNA(miRNA)表达和分泌的变化可作为GDM诊断、预后和治疗的新型标志物。在本综述中,我们总结了外泌体miRNA和循环miRNA在GDM中的各种作用。我们发现某些miRNA表达的变化可用于诊断GDM。外泌体miRNA靶向代谢途径,导致胰岛素抵抗。我们还强调了miRNA和外泌体miRNA用作诊断生物标志物或治疗剂的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfce/8820256/edc6221a83c2/DMSO-15-321-g0001.jpg

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