| Literature DB >> 26149918 |
Xinjie Bao1, Gengfeng Liu2, Yongshuai Jiang3, Qinghua Jiang4, Mingzhi Liao3, Rennan Feng5, Liangcai Zhang6, Guoda Ma7, Shuyan Zhang8, Zugen Chen9, Bin Zhao7, Renzhi Wang10, Keshen Li11, Guiyou Liu12.
Abstract
We previously identified the cell adhesion molecule (CAM) pathway as a consistent signal in 2 Alzheimer's disease (AD) genome-wide association studies (GWAS). However, the genetic mechanisms of the CAM pathway in AD are unclear. Here, we conducted pathway analysis using (1) Kyoto Encyclopedia of Genes and Genomes and Gene Ontology pathways; (2) 4 brain expression GWAS datasets; and (3) 2 whole-genome AD case-control expression datasets. Using the 4 brain expression GWAS datasets, we identified that genes regulated by cis-regulatory single-nucleotide polymorphisms (SNPs) were significantly enriched in the CAM pathway (p = 2.05E-06, p = 6.10E-07, p = 2.05E-06, and p = 1.47E-07 for each dataset). Interestingly, CAM is a significantly enriched pathway using down-regulated genes (raw p = 0.0235 and adjusted p = 0.0305) and all differentially expressed genes (raw p = 0.0105 and adjusted p = 0.0156) in dataset 5, and all differentially expressed genes (raw p = 0.0041 and adjusted p = 0.0062) in dataset 6. Collectively, our results show that CAM pathway genes are regulated by cis-regulatory SNPs and show significantly altered expression in AD. We believe that our results advance the understanding of AD mechanisms and will be useful for future genetic studies of AD.Entities:
Keywords: Alzheimer's disease; Brain expression; Cell adhesion molecules; Genome-wide association studies; Pathway analysis
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Year: 2015 PMID: 26149918 DOI: 10.1016/j.neurobiolaging.2015.06.006
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673