Concerted perturbation observed in a hub network in Alzheimer's disease.

Alzheimer's disease (AD) is a progressive neurodegenerative disease involving the alteration of gene expression at the whole genome level. Genome-wide transcriptional profiling of AD has been conducted by many groups on several relevant brain regions. However, identifying the most critical dys-...

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Main Authors: Dapeng Liang, Guangchun Han, Xuemei Feng, Jiya Sun, Yong Duan, Hongxing Lei
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3398025?pdf=render
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spelling doaj-720cbcc65d31403eadfd42c56e624ff12020-11-24T21:33:55ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0177e4049810.1371/journal.pone.0040498Concerted perturbation observed in a hub network in Alzheimer's disease.Dapeng LiangGuangchun HanXuemei FengJiya SunYong DuanHongxing LeiAlzheimer's disease (AD) is a progressive neurodegenerative disease involving the alteration of gene expression at the whole genome level. Genome-wide transcriptional profiling of AD has been conducted by many groups on several relevant brain regions. However, identifying the most critical dys-regulated genes has been challenging. In this work, we addressed this issue by deriving critical genes from perturbed subnetworks. Using a recent microarray dataset on six brain regions, we applied a heaviest induced subgraph algorithm with a modular scoring function to reveal the significantly perturbed subnetwork in each brain region. These perturbed subnetworks were found to be significantly overlapped with each other. Furthermore, the hub genes from these perturbed subnetworks formed a connected hub network consisting of 136 genes. Comparison between AD and several related diseases demonstrated that the hub network was robustly and specifically perturbed in AD. In addition, strong correlation between the expression level of these hub genes and indicators of AD severity suggested that this hub network can partially reflect AD progression. More importantly, this hub network reflected the adaptation of neurons to the AD-specific microenvironment through a variety of adjustments, including reduction of neuronal and synaptic activities and alteration of survival signaling. Therefore, it is potentially useful for the development of biomarkers and network medicine for AD.http://europepmc.org/articles/PMC3398025?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Dapeng Liang
Guangchun Han
Xuemei Feng
Jiya Sun
Yong Duan
Hongxing Lei
spellingShingle Dapeng Liang
Guangchun Han
Xuemei Feng
Jiya Sun
Yong Duan
Hongxing Lei
Concerted perturbation observed in a hub network in Alzheimer's disease.
PLoS ONE
author_facet Dapeng Liang
Guangchun Han
Xuemei Feng
Jiya Sun
Yong Duan
Hongxing Lei
author_sort Dapeng Liang
title Concerted perturbation observed in a hub network in Alzheimer's disease.
title_short Concerted perturbation observed in a hub network in Alzheimer's disease.
title_full Concerted perturbation observed in a hub network in Alzheimer's disease.
title_fullStr Concerted perturbation observed in a hub network in Alzheimer's disease.
title_full_unstemmed Concerted perturbation observed in a hub network in Alzheimer's disease.
title_sort concerted perturbation observed in a hub network in alzheimer's disease.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Alzheimer's disease (AD) is a progressive neurodegenerative disease involving the alteration of gene expression at the whole genome level. Genome-wide transcriptional profiling of AD has been conducted by many groups on several relevant brain regions. However, identifying the most critical dys-regulated genes has been challenging. In this work, we addressed this issue by deriving critical genes from perturbed subnetworks. Using a recent microarray dataset on six brain regions, we applied a heaviest induced subgraph algorithm with a modular scoring function to reveal the significantly perturbed subnetwork in each brain region. These perturbed subnetworks were found to be significantly overlapped with each other. Furthermore, the hub genes from these perturbed subnetworks formed a connected hub network consisting of 136 genes. Comparison between AD and several related diseases demonstrated that the hub network was robustly and specifically perturbed in AD. In addition, strong correlation between the expression level of these hub genes and indicators of AD severity suggested that this hub network can partially reflect AD progression. More importantly, this hub network reflected the adaptation of neurons to the AD-specific microenvironment through a variety of adjustments, including reduction of neuronal and synaptic activities and alteration of survival signaling. Therefore, it is potentially useful for the development of biomarkers and network medicine for AD.
url http://europepmc.org/articles/PMC3398025?pdf=render
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AT jiyasun concertedperturbationobservedinahubnetworkinalzheimersdisease
AT yongduan concertedperturbationobservedinahubnetworkinalzheimersdisease
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