| Literature DB >> 27989508 |
Nicholas T Seyfried1, Eric B Dammer2, Vivek Swarup3, Divya Nandakumar2, Duc M Duong2, Luming Yin2, Qiudong Deng2, Tram Nguyen2, Chadwick M Hales4, Thomas Wingo5, Jonathan Glass4, Marla Gearing6, Madhav Thambisetty7, Juan C Troncoso8, Daniel H Geschwind3, James J Lah4, Allan I Levey9.
Abstract
Here, we report proteomic analyses of 129 human cortical tissues to define changes associated with the asymptomatic and symptomatic stages of Alzheimer's disease (AD). Network analysis revealed 16 modules of co-expressed proteins, 10 of which correlated with AD phenotypes. A subset of modules overlapped with RNA co-expression networks, including those associated with neurons and astroglial cell types, showing altered expression in AD, even in the asymptomatic stages. Overlap of RNA and protein networks was otherwise modest, with many modules specific to the proteome, including those linked to microtubule function and inflammation. Proteomic modules were validated in an independent cohort, demonstrating some module expression changes unique to AD and several observed in other neurodegenerative diseases. AD genetic risk loci were concentrated in glial-related modules in the proteome and transcriptome, consistent with their causal role in AD. This multi-network analysis reveals protein- and disease-specific pathways involved in the etiology, initiation, and progression of AD.Entities:
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Year: 2016 PMID: 27989508 PMCID: PMC5269514 DOI: 10.1016/j.cels.2016.11.006
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304