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pmid:30124448

Application of Weighted Gene Co-Expression Network Analysis to Explore the Key Genes in Alzheimer's Disease.

Jia-Wei Liang · Zheng-Yu Fang · Yong Huang · Zhen-Yu Liuyang · Xiao-Lin Zhang · Jing-Lin Wang · Hui Wei · Jian-Zhi Wang · Xiao-Chuan Wang · Ji Zeng · Rong Liu

Journal of Alzheimer's disease : JAD · 2018 doi:10.3233/JAD-180400

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:30124448
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title
Application of Weighted Gene Co-Expression Network Analysis to Explore the Key Genes in Alzheimer's Disease.
doi
10.3233/JAD-180400
pmid
30124448
authors array · 11 items
[0]
Jia-Wei Liang
[1]
Zheng-Yu Fang
[2]
Yong Huang
[3]
Zhen-Yu Liuyang
[4]
Xiao-Lin Zhang
[5]
Jing-Lin Wang
[6]
Hui Wei
[7]
Jian-Zhi Wang
[8]
Xiao-Chuan Wang
[9]
Ji Zeng
[10]
Rong Liu
journal
Journal of Alzheimer's disease : JAD
year
2018
abstract
BACKGROUND: Weighted co-expression network analysis (WGCNA) is a powerful systems biology method to describe the correlation of gene expression based on the microarray database, which can be used to facilitate the discovery of therapeutic targets or candidate biomarkers in diseases. OBJECTIVE: To explore the key genes in the development of Alzheimer's disease (AD) by using WGCNA. METHODS: The whole gene expression data GSE1297 from AD and control human hippocampus was obtained from the GEO database in NCBI. Co-expressed genes were clustered into different modules. Modules of interest were identified through calculating the correlation coefficient between the module and phenotypic traits. GO and pathway enrichment analyses were conducted, and the central players (key hub genes) within the modules of interest were identified through network analysis. The expression of the identified key genes was confirmed in AD transgenic mice through using qRT-PCR. RESULTS: Two modules were found to be associated with AD clinical severity, which functioning mainly in mineral absorption, NF-κB signaling, and cGMP-PKG signaling pathways. Through analysis of the two modules, we found that metallothionein (MT), Notch2, MSX1, ADD3, and RAB31 were highly correlated with AD phenotype. Increase in expression of these genes was confirmed in aged AD transgenic mice. CONCLUSION: WGCNA analysis can be used to analyze and predict the key genes in AD. MT1, MT2, MSX1, NOTCH2, ADD3, and RAB31 are identified to be the most relevant genes, which may be potential targets for AD therapy.
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Weighted gene co-expression network analysis (WGCNA) is a popular systems biology method used to describe the correlation of gene expression based on the microarray database [2].
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Weighted gene co-expression network analysis (WGCNA) is a popular systems biology method used to describe the correlation of gene expression based on the microarray database [2].
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The data used in this paper was obtained from the GEO database in NCBI (Gene Expression Omnibus, http://www.ncbi.nlm.gov/geo), and the data entry number is GSE1297.
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sections[3] "Data acquisition and preprocessing" paragraph 2
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The data used in this paper was obtained from the GEO database in NCBI (Gene Expression Omnibus, http://www.ncbi.nlm.gov/geo), and the data entry number is GSE1297.
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Incipient Alzheimer's Disease: Microarray Correlation Analyses
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Gene co-expression network construction and module identification
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ba34b49490d9bfaf
lineage object · 4 fields
parent_id
pmid:30124448
parent_hash
sha256:58be513b0c5260945727abcb86f9a75882a48790678c6689969b99230025aa40
fork_of
null
gaps array · 7 items
[0]
asset:data:geo:GSE1297 licence not read
[1]
asset:data:geo:GSE1297 not downloaded
[2]
execution.not_run
[3]
method.reader_named_unmapped
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review.human_critique
[5]
review.independent_reader
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review.machine_critique
assays array · 2 items
[0] object · 11 fields
role
data_generation
definition_id
microarray
definition_version
99e1195c7d6f
required_operations array · 0 items
support_state
partial
source_hashes object · 1 field
assay_lexicon
99e1195c7d6f
confidence
0.93
evidence array · 1 item
[0]
correlation of gene expression based on the microarray database, which can be used to facilitate th
order_basis
paper_text_order:222
id
assay:1
[1] object · 11 fields
role
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definition_id
network_analysis
definition_version
f2132e96ae6c7a4e
required_operations array · 1 item
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pathway_enrich
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
pathway enrichment
order_basis
consumes_earlier_output
id
assay:2
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:30124448", "kind": "science-record", "revision": 5, "content_hash": "sha256:8b82fe6a13a90192d5118d2fc3c8fed4ba93c193308183b4cc73c1803adecfa5", "created_at": "2026-11-01T15:40:36Z", "updated_at": "2026-11-01T21:21:36Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Application of Weighted Gene Co-Expression Network Analysis to Explore the Key Genes in Alzheimer's Disease.", "doi": "10.3233/JAD-180400", "pmid": "30124448", "authors": ["Jia-Wei Liang", "Zheng-Yu Fang", "Yong Huang", "Zhen-Yu Liuyang", "Xiao-Lin Zhang", "Jing-Lin Wang", "Hui Wei", "Jian-Zhi Wang", "Xiao-Chuan Wang", "Ji Zeng", "Rong Liu"], "journal": "Journal of Alzheimer's disease : JAD", "year": 2018, "abstract": "BACKGROUND: Weighted co-expression network analysis (WGCNA) is a powerful systems biology method to describe the correlation of gene expression based on the microarray database, which can be used to facilitate the discovery of therapeutic targets or candidate biomarkers in diseases.\nOBJECTIVE: To explore the key genes in the development of Alzheimer's disease (AD) by using WGCNA.\nMETHODS: The whole gene expression data GSE1297 from AD and control human hippocampus was obtained from the GEO database in NCBI. Co-expressed genes were clustered into different modules. Modules of interest were identified through calculating the correlation coefficient between the module and phenotypic traits. GO and pathway enrichment analyses were conducted, and the central players (key hub genes) within the modules of interest were identified through network analysis. The expression of the identified key genes was confirmed in AD transgenic mice through using qRT-PCR.\nRESULTS: Two modules were found to be associated with AD clinical severity, which functioning mainly in mineral absorption, NF-κB signaling, and cGMP-PKG signaling pathways. Through analysis of the two modules, we found that metallothionein (MT), Notch2, MSX1, ADD3, and RAB31 were highly correlated with AD phenotype. Increase in expression of these genes was confirmed in aged AD transgenic mice.\nCONCLUSION: WGCNA analysis can be used to analyze and predict the key genes in AD. 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