• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

阿尔茨海默病中转录因子和非编码RNA介导的潜在致病基因模块分析

Analysis of transcription factor- and ncRNA-mediated potential pathogenic gene modules in Alzheimer's disease.

作者信息

Zou Cuihua, Wang Jie, Huang Xiaohua, Jian Chongdong, Zou Donghua, Li Xuebin

机构信息

Department of Neurology, Youjiang Medical University for Nationalities, Baise, Guangxi 533000, People's Republic of China.

Department of Nephrology, Youjiang Medical University for Nationalities, Baise, Guangxi 533000, People's Republic of China.

出版信息

Aging (Albany NY). 2019 Aug 16;11(16):6109-6119. doi: 10.18632/aging.102169.

DOI:10.18632/aging.102169
PMID:31422384
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6738443/
Abstract

Alzheimer's disease (AD) is a progressive neurodegenerative disease that ranks as the fourth most common cause of death in developed countries. In our study, genes differentially expressed between AD and healthy individuals were identified and used to construct protein-protein interaction (PPI) networks. The AD-related PPI network was used to identify functional modules, and enrichment analysis showed that they were significantly involved in "Alzheimer's disease", "apoptosis", and related pathways. We predicted non-coding RNAs and transcription factors that may regulate the functional modules. The expression of hub genes and transcription factors was validated in an independent data set. The results in this study provide several candidates for further research on mechanisms of AD pathogenesis.

摘要

阿尔茨海默病(AD)是一种进行性神经退行性疾病,在发达国家是第四大常见死因。在我们的研究中,鉴定了AD患者与健康个体之间差异表达的基因,并用于构建蛋白质-蛋白质相互作用(PPI)网络。利用AD相关的PPI网络来识别功能模块,富集分析表明它们显著参与了“阿尔茨海默病”、“细胞凋亡”及相关途径。我们预测了可能调节这些功能模块的非编码RNA和转录因子。在一个独立数据集中验证了枢纽基因和转录因子的表达。本研究结果为AD发病机制的进一步研究提供了几个候选对象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d93/6738443/03f2ef4b1f36/aging-11-102169-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d93/6738443/18ba20eb2a44/aging-11-102169-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d93/6738443/cbcc99dbc4f2/aging-11-102169-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d93/6738443/536efe202bbb/aging-11-102169-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d93/6738443/590987f943fa/aging-11-102169-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d93/6738443/03f2ef4b1f36/aging-11-102169-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d93/6738443/18ba20eb2a44/aging-11-102169-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d93/6738443/cbcc99dbc4f2/aging-11-102169-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d93/6738443/536efe202bbb/aging-11-102169-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d93/6738443/590987f943fa/aging-11-102169-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d93/6738443/03f2ef4b1f36/aging-11-102169-g005.jpg

相似文献

1
Analysis of transcription factor- and ncRNA-mediated potential pathogenic gene modules in Alzheimer's disease.阿尔茨海默病中转录因子和非编码RNA介导的潜在致病基因模块分析
Aging (Albany NY). 2019 Aug 16;11(16):6109-6119. doi: 10.18632/aging.102169.
2
Identification of Potential Therapeutic Targets of Alzheimer's Disease By Weighted Gene Co-Expression Network Analysis.通过加权基因共表达网络分析鉴定阿尔茨海默病的潜在治疗靶点
Chin Med Sci J. 2020 Dec 31;35(4):330-341. doi: 10.24920/003695.
3
Condition-specific gene co-expression network mining identifies key pathways and regulators in the brain tissue of Alzheimer's disease patients.特定疾病基因共表达网络挖掘可识别阿尔茨海默病患者脑组织中的关键通路和调节因子。
BMC Med Genomics. 2018 Dec 31;11(Suppl 6):115. doi: 10.1186/s12920-018-0431-1.
4
Exploring Shared Pathogenesis of Alzheimer's Disease and Type 2 Diabetes Mellitus via Co-expression Networks Analysis.通过共表达网络分析探索阿尔茨海默病和2型糖尿病的共同发病机制
Curr Alzheimer Res. 2020;17(6):566-575. doi: 10.2174/1567205017666200810164932.
5
Intrinsic-overlapping co-expression module detection with application to Alzheimer's Disease.基于重叠共表达模块的阿尔茨海默病研究。
Comput Biol Chem. 2018 Dec;77:373-389. doi: 10.1016/j.compbiolchem.2018.10.014. Epub 2018 Nov 9.
6
Construction of Transcriptional Regulatory Network of Alzheimer's Disease Based on PANDA Algorithm.基于 PANDA 算法构建阿尔茨海默病转录调控网络。
Interdiscip Sci. 2019 Jun;11(2):226-236. doi: 10.1007/s12539-018-0297-0. Epub 2018 Apr 19.
7
Genetic networks in Parkinson's and Alzheimer's disease.帕金森病和阿尔茨海默病中的遗传网络。
Aging (Albany NY). 2020 Mar 23;12(6):5221-5243. doi: 10.18632/aging.102943.
8
Hippocampal transcriptome profiling combined with protein-protein interaction analysis elucidates Alzheimer's disease pathways and genes.海马转录组谱分析结合蛋白质-蛋白质相互作用分析阐明阿尔茨海默病的相关通路和基因。
Neurobiol Aging. 2019 Feb;74:225-233. doi: 10.1016/j.neurobiolaging.2018.10.023. Epub 2018 Oct 29.
9
In Silico Analyses for Key Genes and Molecular Genetic Mechanism in Epilepsy and Alzheimer's Disease.癫痫和阿尔茨海默病关键基因的计算机分析及分子遗传机制
CNS Neurol Disord Drug Targets. 2018;17(8):608-617. doi: 10.2174/1871527317666180724150839.
10
Integrative network analysis of nineteen brain regions identifies molecular signatures and networks underlying selective regional vulnerability to Alzheimer's disease.对19个脑区的综合网络分析确定了阿尔茨海默病选择性区域易损性背后的分子特征和网络。
Genome Med. 2016 Nov 1;8(1):104. doi: 10.1186/s13073-016-0355-3.

引用本文的文献

1
Single-Nucleus Landscape of Glial Cells and Neurons in Alzheimer's Disease.阿尔茨海默病中神经胶质细胞和神经元的单核图谱
Mol Neurobiol. 2025 Mar;62(3):2695-2709. doi: 10.1007/s12035-024-04428-6. Epub 2024 Aug 17.
2
Downregulation of miR-181c-5p in Alzheimer's disease weakens the response of microglia to Aβ phagocytosis.阿尔茨海默病中 miR-181c-5p 的下调削弱了小胶质细胞对 Aβ 吞噬的反应。
Sci Rep. 2024 May 20;14(1):11487. doi: 10.1038/s41598-024-62347-x.
3
Long Non-coding RNA ANRIL and Its Role in the Development of Age-Related Diseases.

本文引用的文献

1
The role of gut microbiota in pathogenesis of Alzheimer's disease.肠道微生物群在阿尔茨海默病发病机制中的作用。
J Appl Microbiol. 2019 Oct;127(4):954-967. doi: 10.1111/jam.14264. Epub 2019 Apr 15.
2
Apathy in Alzheimer's disease.阿尔茨海默病中的冷漠。
Curr Opin Behav Sci. 2018 Aug;22:7-13. doi: 10.1016/j.cobeha.2017.12.007.
3
Phenylpropanoids and Alzheimer's disease: A potential therapeutic platform.苯丙素类化合物与阿尔茨海默病:一个有潜力的治疗平台。
长链非编码 RNA ANRIL 及其在与年龄相关疾病发展中的作用。
Mol Neurobiol. 2024 Oct;61(10):7919-7929. doi: 10.1007/s12035-024-04074-y. Epub 2024 Mar 5.
4
Exploration of novel biomarkers in Alzheimer's disease based on four diagnostic models.基于四种诊断模型探索阿尔茨海默病的新型生物标志物
Front Aging Neurosci. 2023 Feb 16;15:1079433. doi: 10.3389/fnagi.2023.1079433. eCollection 2023.
5
Potential biomarkers of Alzheimer's disease and cerebral small vessel disease.阿尔茨海默病和脑小血管病的潜在生物标志物。
Front Mol Neurosci. 2022 Oct 10;15:996107. doi: 10.3389/fnmol.2022.996107. eCollection 2022.
6
Exploring Early Physical Examination Diagnostic Biomarkers for Alzheimer's Disease Based on Least Absolute Shrinkage and Selection Operator.基于最小绝对值收缩和选择算子的阿尔茨海默病早期体格检查诊断生物标志物研究。
Comput Math Methods Med. 2022 Aug 18;2022:3039248. doi: 10.1155/2022/3039248. eCollection 2022.
7
Identification of molecular signatures associated with sleep disorder and Alzheimer's disease.与睡眠障碍和阿尔茨海默病相关的分子特征的鉴定。
Front Psychiatry. 2022 Aug 4;13:925012. doi: 10.3389/fpsyt.2022.925012. eCollection 2022.
8
REPS1 as a Potential Biomarker in Alzheimer's Disease and Vascular Dementia.REPS1作为阿尔茨海默病和血管性痴呆的潜在生物标志物。
Front Aging Neurosci. 2022 Jun 22;14:894824. doi: 10.3389/fnagi.2022.894824. eCollection 2022.
9
Identification of Alzheimer's Disease Molecular Subtypes Based on Parallel Large-Scale Sequencing.基于平行大规模测序的阿尔茨海默病分子亚型鉴定
Front Aging Neurosci. 2022 Apr 28;14:770136. doi: 10.3389/fnagi.2022.770136. eCollection 2022.
10
Microglia Mediate the Occurrence and Development of Alzheimer's Disease Through Ligand-Receptor Axis Communication.小胶质细胞通过配体-受体轴通讯介导阿尔茨海默病的发生和发展。
Front Aging Neurosci. 2021 Sep 20;13:731180. doi: 10.3389/fnagi.2021.731180. eCollection 2021.
Neurochem Int. 2018 Nov;120:99-111. doi: 10.1016/j.neuint.2018.08.001. Epub 2018 Aug 8.
4
Mitochondria and Calcium Regulation as Basis of Neurodegeneration Associated With Aging.线粒体与钙调节作为衰老相关神经退行性变的基础
Front Neurosci. 2018 Jul 13;12:470. doi: 10.3389/fnins.2018.00470. eCollection 2018.
5
[MALAT1 inhibits proliferation and promotes apoptosis of SH-SY5Y cells induced by Aβ via blocking PI3K/mTOR/GSK3β pathway].[MALAT1通过阻断PI3K/mTOR/GSK3β信号通路抑制Aβ诱导的SH-SY5Y细胞增殖并促进其凋亡]
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2018 May;34(5):434-441.
6
Effect of microRNA-186 on oxidative stress injury of neuron by targeting interleukin 2 through the janus kinase-signal transducer and activator of transcription pathway in a rat model of Alzheimer's disease.miRNA-186 通过 Janus 激酶-信号转导与转录激活因子通路靶向白细胞介素 2 对阿尔茨海默病大鼠模型神经元氧化应激损伤的影响。
J Cell Physiol. 2018 Dec;233(12):9488-9502. doi: 10.1002/jcp.26843. Epub 2018 Jul 11.
7
Modulation in miR-200a/SIRT1axis is associated with apoptosis in MPP-induced SH-SY5Y cells.miR-200a/SIRT1 轴的调节与 MPP 诱导的 SH-SY5Y 细胞凋亡有关。
Gene. 2018 Oct 20;674:25-30. doi: 10.1016/j.gene.2018.06.061. Epub 2018 Jun 21.
8
Comparative transcriptomics of choroid plexus in Alzheimer's disease, frontotemporal dementia and Huntington's disease: implications for CSF homeostasis.阿尔茨海默病、额颞叶痴呆和亨廷顿病脉络丛的比较转录组学:对 CSF 动态平衡的影响。
Fluids Barriers CNS. 2018 May 31;15(1):18. doi: 10.1186/s12987-018-0102-9.
9
MicroRNA expression data analysis to identify key miRNAs associated with Alzheimer's disease.miRNA 表达数据分析鉴定与阿尔茨海默病相关的关键 miRNAs。
J Gene Med. 2018 Jun;20(6):e3014. doi: 10.1002/jgm.3014. Epub 2018 May 21.
10
Preclinical studies using miR-32-5p to suppress clear cell renal cell carcinoma metastasis via altering the miR-32-5p/TR4/HGF/Met signaling.利用 miR-32-5p 抑制透明细胞肾细胞癌转移的临床前研究:通过改变 miR-32-5p/TR4/HGF/Met 信号。
Int J Cancer. 2018 Jul 1;143(1):100-112. doi: 10.1002/ijc.31289. Epub 2018 Apr 2.