Mingyang Cai, Siru Yan, Yaxuan Sun, Qing Huo, Xueling Dai
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引用次数: 0
Abstract
Alzheimer's disease (AD) is a progressive neurodegenerative disorder characterized by amyloid-beta (Aβ) plaque deposition, neurofibrillary tangles of hyperphosphorylated tau protein, and chronic neuroinflammation, leading to synaptic dysfunction and cognitive decline. Current diagnostic methods rely on clinical symptoms and limited biomarkers, while available treatments only provide symptomatic relief without halting disease progression. MicroRNAs (miRNAs), small non-coding RNAs of 19-22 nucleotides, have emerged as crucial regulators of gene expression through post-transcriptional mechanisms and show distinct dysregulation patterns in AD patients' blood, cerebrospinal fluid (CSF), and brain tissues. Key miRNAs such as miR-132, miR-146a, miR-34a, and miR-125b demonstrate consistent alterations in expression levels, correlating with disease progression and offering potential as non-invasive diagnostic tools. This review comprehensively examines the dual role of miRNAs as diagnostic biomarkers and therapeutic targets for AD. We also provide an analysis of specific miRNA signatures in different biofluids (plasma, serum, CSF) and brain regions that correlate with disease stages, highlighting their potential for early and non-invasive diagnosis. Therapeutically, miRNAs modulate multiple AD-related pathways, including neuroinflammation via NF-κB signaling, Aβ production through BACE1 inhibition, and tau phosphorylation via GSK3β regulation. miRNAs also influence synaptic plasticity, mitochondrial function, and autophagy, presenting multifaceted opportunities for intervention. However, challenges, including miRNA heterogeneity, stability, and targeted delivery, remain critical impediments. Advances in nanocarriers, exosomal miRNAs, and viral vectors show promise in overcoming these obstacles, enabling precise miRNA modulation. In addition, we underscore the need for standardized protocols, further validation in clinical cohorts, and the development of cost-effective detection methods to translate miRNA-based approaches into practical diagnostics and therapies. By integrating miRNA biomarkers with existing diagnostic tools and exploring combinatorial therapeutic strategies, researchers can harness the potential of miRNAs to revolutionize AD intervention, paving the way for early detection and effective treatment of this devastating disease.
阿尔茨海默病(AD)是一种进行性神经退行性疾病,其特征是淀粉样β (a β)斑块沉积、tau蛋白过度磷酸化的神经原纤维缠结和慢性神经炎症,导致突触功能障碍和认知能力下降。目前的诊断方法依赖于临床症状和有限的生物标志物,而现有的治疗方法只能提供症状缓解,而不能阻止疾病进展。MicroRNAs (miRNAs)是19-22个核苷酸的小非编码rna,通过转录后机制成为基因表达的关键调节因子,并在AD患者的血液、脑脊液(CSF)和脑组织中显示出明显的失调模式。miR-132、miR-146a、miR-34a和miR-125b等关键mirna在表达水平上表现出一致的变化,与疾病进展相关,并具有作为非侵入性诊断工具的潜力。这篇综述全面探讨了mirna作为AD的诊断生物标志物和治疗靶点的双重作用。我们还提供了与疾病阶段相关的不同生物流体(血浆、血清、脑脊液)和大脑区域中特定miRNA特征的分析,强调了它们在早期和非侵入性诊断中的潜力。在治疗上,mirna调节多种ad相关通路,包括通过NF-κB信号传导的神经炎症,通过BACE1抑制的Aβ产生,以及通过GSK3β调节的tau磷酸化。mirna还影响突触可塑性、线粒体功能和自噬,为干预提供了多方面的机会。然而,挑战,包括miRNA的异质性、稳定性和靶向递送,仍然是关键的障碍。纳米载体、外泌体miRNA和病毒载体的进展有望克服这些障碍,实现精确的miRNA调节。此外,我们强调需要标准化的方案,在临床队列中进一步验证,以及开发具有成本效益的检测方法,将基于mirna的方法转化为实用的诊断和治疗方法。通过将miRNA生物标志物与现有的诊断工具相结合,并探索组合治疗策略,研究人员可以利用miRNA的潜力来彻底改变AD干预,为早期发现和有效治疗这种毁灭性疾病铺平道路。