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阿尔茨海默病中与 secretases 相关的 miRNAs:生物标志物发现的新方法。

Secretases-related miRNAs in Alzheimer's disease: new approach for biomarker discovery.

机构信息

Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran.

Cellular and Molecular Research Center, Department of Anatomy, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran.

出版信息

Neurol Sci. 2017 Nov;38(11):1921-1926. doi: 10.1007/s10072-017-3086-3. Epub 2017 Aug 8.

Abstract

Amyloid-β (Aβ) as a crucial factor in pathogenesis of Alzheimer's disease (AD) is derived from amyloid precursor protein (APP) through a proteolytic process catalyzing by β- and γ-secretase-in amyloidogenesis pathway. Products of α-secretase cleavage also have protective effects against Aβ toxicity. According to existing evidences, microRNAs (miRNAs) show a unique pattern of expression in AD. Moreover, miRNAs regulatory effects on expression of secretases and their main components have been demonstrated in AD. The miRNAs levels may be changed in preclinical conditions and may be considered as diagnostic biomarkers in AD. Therefore, in this paper, we review the miRNAs involved in APP cleavage pathways and the formation of Aβ in order to evaluate the potential diagnostic biomarkers in AD.

摘要

淀粉样蛋白-β(Aβ)作为阿尔茨海默病(AD)发病机制中的关键因素,是通过β-和γ-分泌酶在淀粉样蛋白生成途径中催化淀粉样前体蛋白(APP)产生的。α-分泌酶切割的产物也对 Aβ 毒性具有保护作用。根据现有证据,微小 RNA(miRNA)在 AD 中表现出独特的表达模式。此外,miRNA 对 AD 中分泌酶及其主要成分表达的调节作用已得到证实。miRNA 水平可能在临床前条件下发生变化,并可能被视为 AD 的诊断生物标志物。因此,在本文中,我们综述了参与 APP 切割途径和 Aβ形成的 miRNA,以评估 AD 中的潜在诊断生物标志物。

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