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循环 microRNAs 作为急性脑卒中的生物标志物。

Circulating microRNAs as biomarkers of acute stroke.

机构信息

Department of Biochemistry and Neuroscience Research Centre, Centre for Translational Medicine, Yong Loo Lin School of Medicine, National University of Singapore, 14 Medical Drive, Singapore 117599, Singapore.

出版信息

Int J Mol Sci. 2014 Jan 20;15(1):1418-32. doi: 10.3390/ijms15011418.

Abstract

MicroRNAs have been identified as key regulators of gene expression and thus their potential in disease diagnostics, prognosis and therapy is being actively pursued. Deregulation of microRNAs in cerebral pathogenesis has been reported to a limited extent in both animal models and human. Due to the complexity of the pathology, identifying stroke specific microRNAs has been a challenge. This study shows that microRNA profiles reflect not only the temporal progression of stroke but also the specific etiologies. A panel of 32 microRNAs, which could differentiate stroke etiologies during acute phase was identified and verified using a customized TaqMan Low Density Array (TLDA). Furthermore we also found 5 microRNAs, miR-125b-2*, -27a*, -422a, -488 and -627 to be consistently altered in acute stroke irrespective of age or severity or confounding metabolic complications. Differential expression of these 5 microRNAs was also observed in rat stroke models. Hence, their specificity to the stroke pathology emphasizes the possibility of developing these microRNAs into accurate and useful tools for diagnosis of stroke.

摘要

MicroRNAs 已被鉴定为基因表达的关键调节剂,因此它们在疾病诊断、预后和治疗中的潜力正在被积极探索。在动物模型和人类中,已经有报道称,microRNAs 在脑发病机制中的失调程度有限。由于病理的复杂性,确定中风特异性 microRNAs 一直是一个挑战。本研究表明,microRNA 谱不仅反映了中风的时间进展,也反映了特定的病因。通过使用定制的 TaqMan 低密度阵列 (TLDA),我们鉴定并验证了一组 32 个 microRNAs,这些 microRNAs 可在急性期区分中风的病因。此外,我们还发现 5 个 microRNAs(miR-125b-2*、-27a*、-422a、-488 和 -627)在急性中风中无论年龄、严重程度或混杂的代谢并发症如何均持续发生改变。在大鼠中风模型中也观察到这些 5 个 microRNAs 的差异表达。因此,这些 microRNAs 对中风病理的特异性强调了将这些 microRNAs 开发成准确、有用的中风诊断工具的可能性。

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