白细胞端粒长度相关 lncRNA NBR2 在阿尔茨海默病中的作用研究

IF 3.9 3区 医学 Q2 CELL BIOLOGY Aging-Us Pub Date : 2024-09-16 DOI:10.18632/aging.206107
Wenjie Li,Haoyan Chen,Xiaofan Yuan,Qi Yao,Mingjiong Zhang
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引用次数: 0

摘要

阿尔茨海默氏症(AD)是一种神经退行性疾病,好发于中老年人。随着病情的发展,患者会逐渐丧失生活自理能力,给家庭带来沉重负担。白细胞端粒长度(LTL)与认知能力之间存在联系。为了寻找可能的致病机制和潜在的治疗药物,我们利用孟德尔随机分析法(MR)证明了LTL与AD之间的因果关系。我们进一步探讨了靶基因NBR2和下游mRNA GJA1及GJA1相关基因的表达、通路富集以及与免疫细胞的关联。利用基因簇-药物靶点相互作用网络,我们获得了潜在的治疗药物。我们的研究为AD与LTL之间的因果联系提供了证据,并提出了可能治疗和缓解AD症状的药物。
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Study of the role of leukocyte telomere length-related lncRNA NBR2 in Alzheimer's disease.
Alzheimer's Syndrome (AD) is a neurodegenerative disease that is prevalent in middle-aged and elderly people. As the disease progresses, patients gradually lose the ability to take care of themselves, which brings a heavy burden to the family. There is a link between leukocyte telomere length (LTL) and cognitive ability. To search for possible pathogenic mechanisms and potential therapeutic agents, we demonstrated a causal link between LTL and AD using Mendelian randomization analysis (MR). The expression of the target gene NBR2 and the downstream mRNA GJA1 and GJA1-related genes, pathway enrichment, and association with immune cells were further explored. Using the gene cluster-drug target interaction network, we obtained potential therapeutic drugs. Our study provides evidence for a causal link between AD and LTL, suggesting medicines that may treat and alleviate AD symptoms.
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来源期刊
Aging-Us
Aging-Us CELL BIOLOGY-
CiteScore
10.00
自引率
0.00%
发文量
595
审稿时长
6-12 weeks
期刊介绍: Information not localized
期刊最新文献
Cross species activity of TERT human telomerase component. Stage-dependent transcriptomic changes in human dermal fibroblast senescence model. From Hydra to rotifer and beyond: implications for human aging and delayed senescence. Association of epigenetic age acceleration with MRI biomarkers of aging and Alzheimer's disease neurodegeneration. Toward actionable interventions in human aging (12th ARDD meeting, 2025).
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