MicroRNAs as Biomarkers for Birth Defects.

Ratnam S Seelan, M Michele Pisano, Robert M Greene
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引用次数: 0

Abstract

It is estimated that 2-4% of live births will have a birth defect (BD). The availability of biomarkers for the prenatal detection of BDs will facilitate early risk assessment, prompt medical intervention and ameliorating disease severity. miRNA expression levels are often found to be altered in many diseases. There is, thus, a growing interest in determining whether miRNAs, particularly extracellular miRNAs, can predict, diagnose, or monitor BDs. These miRNAs, typically encapsulated in exosomes, are released by cells (including those of the fetus and placenta) into the extracellular milieu, such as blood, urine, saliva and cerebrospinal fluid, thereby enabling interaction with target cells. Exosomal miRNAs are stable, protected from degradation, and retain functionality. The observation that placental and fetal miRNAs can be detected in maternal serum, provides a strong rationale for adopting miRNAs as noninvasive prenatal biomarkers for BDs. In this mini-review, we examine the current state of research involving the use of miRNAs as prognostic and diagnostic biomarkers for BD.

作为出生缺陷生物标志物的微RNA。
据估计,2-4% 的活产婴儿会有出生缺陷(BD)。产前检测出生缺陷的生物标志物将有助于早期风险评估、及时的医疗干预和改善疾病的严重程度。因此,人们对确定 miRNA(尤其是细胞外 miRNA)是否能预测、诊断或监测 BDs 越来越感兴趣。这些 miRNA 通常包裹在外泌体中,由细胞(包括胎儿和胎盘的细胞)释放到细胞外环境(如血液、尿液、唾液和脑脊液)中,从而与靶细胞相互作用。外泌体 miRNA 比较稳定,不会被降解,并能保持功能。观察发现胎盘和胎儿 miRNA 可在母体血清中检测到,这为采用 miRNA 作为无创产前生物标记物检测 BDs 提供了强有力的依据。在这篇微型综述中,我们将探讨目前使用 miRNA 作为 BD 预后和诊断生物标志物的研究现状。
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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