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pmid:32626989

Integrated microarray analysis to identify potential biomarkers and therapeutic targets in dilated cardiomyopathy.

Hao Zhang · Junyu Huo · Wanying Jiang · Qijun Shan

Molecular medicine reports · 2020 doi:10.3892/mmr.2020.11145

Paper

complete

Experiment

complete

Data

partial

Analysis

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Execution

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title
Integrated microarray analysis to identify potential biomarkers and therapeutic targets in dilated cardiomyopathy.
doi
10.3892/mmr.2020.11145
pmid
32626989
authors array · 4 items
[0]
Hao Zhang
[1]
Junyu Huo
[2]
Wanying Jiang
[3]
Qijun Shan
journal
Molecular medicine reports
year
2020
abstract
Dilated cardiomyopathy (DCM) is a primary cardiomyopathy with high mortality. The aim of the present study was to identify the related genes in DCM. The four expression profiles (GSE17800, GSE21610, GSE42955 and GSE79962) downloaded from the Gene Expression Omnibus (GEO) database were analyzed using RankProd and metaMA R packages to identify differentially expressed genes (DEGs). DEGs were uploaded to the Database for Annotation, Visualization and Integrated Discovery (DAVID), for Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis. A protein‑protein interaction (PPI) network of the DEGs was constructed using the STRING database. In addition, hub genes were identified using the Cytoscape plugin cytoHubba. A mouse DCM model, which established via intraperitoneal injection with doxorubicin (DOX), was used to validate the hub genes. A total of 898 DEGs were identified across the four microarrays. Furthermore, GO analysis demonstrated that these DEGs were mainly enriched in cell adhesion, negative regulation of cell proliferation, negative regulation of apoptotic process and potassium ion transport. In addition, KEGG analysis revealed that DEGs were mainly enriched in the ECM‑receptor interaction, the p53 signaling pathway, cardiac muscle contraction and the hypoxia‑inducible factor signaling pathway. Proenkephalin (PENK), chordin like 1 (CHRDL1), calumenin (CALU), apolipoprotein L1, insulin‑like growth factor binding protein 3 (IGFBP3) and ceruloplasmin (CP) were identified as hub genes in the PPI network. Furthermore, the expression levels of PENK, CHRDL1, IGFBP3, CP and CALU in hearts with DCM were validated using a mouse model. In conclusion, the present study identified six hub genes related to DCM. Therefore, the present results may provide a potential mechanism for DCM involving these hub genes, which may serve as biomarkers for screening and diagnosis in the clinic.
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The merged expression matrix was processed using metaMA and RankProd according to the reference manuals, and overlapping genes from the two methods were deemed as DEGs.
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The merged expression matrix was processed using metaMA and RankProd according to the reference manuals, and overlapping genes from the two methods were deemed as DEGs.
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Top 30 upregulated differentially expressed genes.
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Top 30 upregulated differentially expressed genes.
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2.53
[2]
1.40×10−22
[6] array · 3 items
[0]
EIF1AY
[1]
2.45
[2]
1.82×10−22
[7] array · 3 items
[0]
PHLDA1
[1]
1.99
[2]
4.61×10−22
[8] array · 3 items
[0]
LTBP2
[1]
2.06
[2]
7.48×10−20
[9] array · 3 items
[0]
THBS4
[1]
2.05
[2]
2.12×10−19
[10] array · 3 items
[0]
FRZB
[1]
2.07
[2]
5.42×10−19
[11] array · 3 items
[0]
POSTN
[1]
1.91
[2]
5.71×10−19
[12] array · 3 items
[0]
MXRA5
[1]
1.82
[2]
1.01×10−18
[13] array · 3 items
[0]
CCN2
[1]
1.96
[2]
6.47×10−18
[14] array · 3 items
[0]
OMD
[1]
2.00
[2]
6.13×10−18
[15] array · 3 items
[0]
TNNT1
[1]
1.91
[2]
1.12×10−17
[16] array · 3 items
[0]
PRELP
[1]
2.06
[2]
1.34×10−17
[17] array · 3 items
[0]
ASPN
[1]
1.81
[2]
5.31×10−17
[18] array · 3 items
[0]
FMOD
[1]
1.94
[2]
7.19×10−17
[19] array · 3 items
[0]
CCDC80
[1]
1.79
[2]
1.42×10−16
[20] array · 3 items
[0]
RGS4
[1]
1.84
[2]
1.04×10−15
[21] array · 3 items
[0]
SERPINE2
[1]
1.70
[2]
2.58×10−15
[22] array · 3 items
[0]
USP9Y
[1]
1.68
[2]
2.78×10−15
[23] array · 3 items
[0]
STAT4
[1]
1.90
[2]
2.77×10−15
[24] array · 3 items
[0]
PLCE1
[1]
1.75
[2]
2.67×10−15
[25] array · 3 items
[0]
UCHL1
[1]
1.80
[2]
3.19×10−15
[26] array · 3 items
[0]
OGN
[1]
1.74
[2]
1.08×10−14
[27] array · 3 items
[0]
HSPA2
[1]
1.72
[2]
2.10×10−14
[28] array · 3 items
[0]
NAP1L3
[1]
1.77
[2]
3.88×10−14
[29] array · 3 items
[0]
MFAP4
[1]
1.68
[2]
4.80×10−14
[30] array · 3 items
[0]
JAK2
[1]
1.70
[2]
1.27×10−13
locator
section[15]/table-wrap[1]#tIII-mmr-22-02-0915
[9] object · 16 fields
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asset:table:pmid:32626989:4
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table
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jats-table
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application/vnd.jats.table+json
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null
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sha256:438347af2cda44f4e4ee7b4c9f2331d1b354e178d7751cb483599dd4f58dc620
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1284
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open
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verified
reader
read_table
reader_status
available
identifier
section[15]/table-wrap[2]#tIV-mmr-22-02-0915
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null
note
Top 30 downregulated differentially expressed genes.
structure object · 5 fields
pmcid
PMC7339620
section_index
15
section_title
Identification of DEGs between patients with DCM and healthy controls
row_count
31
column_count
3
table object · 8 fields
label
Table IV.
caption
Top 30 downregulated differentially expressed genes.
rows array · 31 items
[0] array · 3 items
[0]
Downregulated gene
[1]
Fold change
[2]
Percentage of false prediction
[1] array · 3 items
[0]
MYH6
[1]
0.32
[2]
2.33×10−38
[2] array · 3 items
[0]
ETNPPL
[1]
0.39
[2]
6.74×10−29
[3] array · 3 items
[0]
SERPINA3
[1]
0.38
[2]
1.88×10−27
[4] array · 3 items
[0]
DHRS7C
[1]
0.45
[2]
1.51×10−25
[5] array · 3 items
[0]
AQP4
[1]
0.52
[2]
1.29×10−20
[6] array · 3 items
[0]
CCL2
[1]
0.47
[2]
1.89×10−17
[7] array · 3 items
[0]
LYVE1
[1]
0.58
[2]
2.19×10−16
[8] array · 3 items
[0]
LSAMP
[1]
0.53
[2]
2.69×10−16
[9] array · 3 items
[0]
DLK1
[1]
0.53
[2]
6.81×10−16
[10] array · 3 items
[0]
CORIN
[1]
0.53
[2]
1.04×10−15
[11] array · 3 items
[0]
HOPX
[1]
0.55
[2]
1.92×10−15
[12] array · 3 items
[0]
CA14
[1]
0.55
[2]
4.94×10−15
[13] array · 3 items
[0]
RARRES1
[1]
0.54
[2]
8.04×10−15
[14] array · 3 items
[0]
CD163
[1]
0.62
[2]
9.97×10−15
[15] array · 3 items
[0]
KCNIP2
[1]
0.60
[2]
1.01×10−14
[16] array · 3 items
[0]
C1orf105
[1]
0.57
[2]
1.20×10−14
[17] array · 3 items
[0]
CD14
[1]
0.56
[2]
3.45×10−14
[18] array · 3 items
[0]
F13A1
[1]
0.61
[2]
1.53×10−13
[19] array · 3 items
[0]
F5
[1]
0.82
[2]
2.01×10−13
[20] array · 3 items
[0]
TOGARAM2
[1]
0.60
[2]
2.15×10−13
[21] array · 3 items
[0]
CPNE4
[1]
0.59
[2]
2.05×10−12
[22] array · 3 items
[0]
AQP3
[1]
0.62
[2]
4.89×10−12
[23] array · 3 items
[0]
VSIG4
[1]
0.67
[2]
1.31×10−11
[24] array · 3 items
[0]
HEY2
[1]
0.63
[2]
5.73×10−11
[25] array · 3 items
[0]
PLIN2
[1]
0.62
[2]
6.50×10−11
[26] array · 3 items
[0]
SELE
[1]
0.57
[2]
1.46×10−10
[27] array · 3 items
[0]
ADAMTS9
[1]
0.63
[2]
1.71×10−10
[28] array · 3 items
[0]
NAMPT
[1]
0.65
[2]
1.90×10−10
[29] array · 3 items
[0]
SLCO5A1
[1]
0.60
[2]
2.63×10−10
[30] array · 3 items
[0]
HINT3
[1]
0.60
[2]
9.40×10−10
locator
section[15]/table-wrap[2]#tIV-mmr-22-02-0915
[10] object · 16 fields
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asset:table:pmid:32626989:5
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table
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jats-table
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application/vnd.jats.table+json
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null
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sha256:fcb8e582938df4296789acd24a7548307489ec0bb8a58613acfa919b410dc97c
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read_table
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available
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section[19]/table-wrap[1]#tV-mmr-22-02-0915
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Topological properties of hub genes.
structure object · 5 fields
pmcid
PMC7339620
section_index
19
section_title
Construction of the PPI network, and identification of important modules and hub genes
row_count
7
column_count
8
table object · 8 fields
label
Table V.
caption
Topological properties of hub genes.
rows array · 7 items
[0] array · 8 items
[0]
Hub gene
[1]
Degree
[2]
MCC
[3]
DMNC
[4]
MNC
[5]
Fold change
[6]
Percentage of false prediction
[7]
Expression change
[1] array · 8 items
[0]
PENK
[1]
19
[2]
8.72×1010
[3]
1.02476
[4]
14
[5]
1.71
[6]
8.04×10−13
[7]
Upregulated
[2] array · 8 items
[0]
CHRDL1
[1]
16
[2]
8.72×1010
[3]
1.02476
[4]
14
[5]
1.31
[6]
8.04×10−6
[7]
Upregulated
[3] array · 8 items
[0]
CALU
[1]
16
[2]
8.72×1010
[3]
0.92137
[4]
15
[5]
0.84
[6]
1.85×10−2
[7]
Downregulated
[4] array · 8 items
[0]
APOL1
[1]
15
[2]
8.72×1010
[3]
0.92137
[4]
15
[5]
0.77
[6]
5.89×10−3
[7]
Downregulated
[5] array · 8 items
[0]
IGFBP3
[1]
15
[2]
8.72×1010
[3]
0.92137
[4]
15
[5]
1.37
[6]
9.86×10−6
[7]
Upregulated
[6] array · 8 items
[0]
CP
[1]
15
[2]
8.72×1010
[3]
1.02476
[4]
14
[5]
1.32
[6]
2.98×10−6
[7]
Upregulated
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section[19]/table-wrap[1]#tV-mmr-22-02-0915
gaps array · 10 items
[0]
asset:data:geo:GSE17800 not downloaded
[1]
asset:data:geo:GSE17800 licence not read
[2]
asset:data:geo:GSE21610 not downloaded
[3]
asset:data:geo:GSE21610 licence not read
[4]
asset:data:geo:GSE3585 not downloaded
[5]
asset:data:geo:GSE3585 licence not read
[6]
asset:data:geo:GSE42955 not downloaded
[7]
asset:data:geo:GSE42955 licence not read
[8]
asset:data:geo:GSE79962 not downloaded
[9]
asset:data:geo:GSE79962 licence not read
analysis object · 4 fields
state
partial
methods array · 3 items
[0] object · 10 fields
id
method-1
family
network_analysis
specific
ppi_network
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Network / pathway analysis
dsl_operations array · 3 items
[0]
build_graph
[1]
centrality_scores
[2]
pathway_enrich
missing_operations array · 0 items
parameters object · 0 fields
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[0]
edge_list
evidence object · 3 fields
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0.7
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medium
quote
PPI
[1] object · 10 fields
id
method-2
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network_analysis
specific
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Network / pathway analysis
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[0]
pathway_enrich
missing_operations array · 0 items
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data_shapes array · 1 item
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edge_list
evidence object · 3 fields
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0.7
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medium
quote
pathway enrichment
[2] object · 10 fields
id
method-3
family
null
specific
null
label
Meta-analysis of differentially expressed genes using metaMA and RankProd
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parameters object · 0 fields
data_shapes array · 0 items
evidence object · 3 fields
score
1
band
verbatim
quote
The merged expression matrix was processed using metaMA and RankProd according to the reference manuals, and overlapping genes from the two methods were deemed as DEGs.
targets array · 0 items
gaps array · 1 item
[0]
method.reader_named_unmapped
capability object · 3 fields
state
complete
requirements array · 1 item
[0] object · 6 fields
capability_id
capability:computational_analysis
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Computational analysis platform
assay_families array · 9 items
[0]
meta_analysis
[1]
machine_learning
[2]
survival_analysis
[3]
statistical_regression
[4]
pca
[5]
molecular_docking
[6]
network_analysis
[7]
differential_expression
[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
state
complete
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R1
blocked_on
nothing:replicable_now
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method object · 5 fields
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R1
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true
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build_graph
[1]
centrality_scores
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pathway_enrich
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: ppi_network.
capability object · 4 fields
tier
R1
capability_id
capability:computational_analysis
availability_state
owned
basis
The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
tier
R1
reachable
true
accessions array · 5 items
[0]
GSE17800
[1]
GSE21610
[2]
GSE42955
[3]
GSE79962
[4]
GSE3585
resolved_accessions array · 5 items
[0]
GSE17800
[1]
GSE21610
[2]
GSE42955
[3]
GSE79962
[4]
GSE3585
statements array · 1 item
[0]
All data generated or analyzed during this study are included in this published article.
basis
The paper names GSE17800, GSE21610, GSE42955, GSE79962, GSE3585 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
dsl_operations array · 3 items
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build_graph
[1]
centrality_scores
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pathway_enrich
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source:pmid:32626989
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data:geo:GSE17800
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asset:table:pmid:32626989:1
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asset:table:pmid:32626989:2
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asset:table:pmid:32626989:3
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asset:table:pmid:32626989:4
[6]
asset:table:pmid:32626989:5
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run_analysis
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data:geo:GSE17800
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partial
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extraction_review
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MiniMax-M3.1-Flash
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minimax
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minimax
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2026-10-31T18:21:02Z
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single_reader
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verbatim
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verbatim
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3
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37536
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12680
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id
extraction
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minimax
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review.human_critique
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not_run
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execution.not_run
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pmid:32626989
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paper
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pmid:32626989
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source:pmid:32626989
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PMID 32626989 full text
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data:geo:GSE17800
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GEO GSE17800
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activity-reading-sci-2026-11-01
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classification
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pmid:32626989
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pmid:32626989
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source:pmid:32626989
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PMID 32626989 full text
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data:geo:GSE17800
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GEO GSE17800
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agent:corpus-assay-engine
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activity-read-32626989
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source:pmid:32626989
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agent:minimax-reader
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activity-resolve-GSE17800
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accession_resolution
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data:geo:GSE17800
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agent:corpus-assay-engine
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agent:corpus-assay-engine
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Corpus assay engine
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agent:minimax-reader
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MiniMax literature reader
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dsl_catalogue_fingerprint
343fb30756ba6ec3
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lineage object · 4 fields
parent_id
pmid:32626989
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sha256:380c2e7e3a48982a7243d93beb6b5c48db53700f6ba43a9a57a40c91f54f6941
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null
gaps array · 15 items
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asset:data:geo:GSE17800 licence not read
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asset:data:geo:GSE17800 not downloaded
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[3]
asset:data:geo:GSE21610 not downloaded
[4]
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[5]
asset:data:geo:GSE3585 not downloaded
[6]
asset:data:geo:GSE42955 licence not read
[7]
asset:data:geo:GSE42955 not downloaded
[8]
asset:data:geo:GSE79962 licence not read
[9]
asset:data:geo:GSE79962 not downloaded
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data_generation
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microarray
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99e1195c7d6f
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partial
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99e1195c7d6f
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[0]
Integrated microarray analysis to identify potential biomarkers an
[1]
s. MetaMA (v 3.1.2) (13) is an R package for microarray DEG meta-analyses that uses moderated effect
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paper_text_order:0
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data_generation
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99e1195c7d6f
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99e1195c7d6f
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[0]
LU in hearts with DCM were validated using a mouse model. In conclusion, the present study identified
[1]
fied using the Cytoscape plugin cytoHubba. A mouse DCM model, which established via intraperito
[2]
LU in hearts with DCM were validated using a mouse model. In conclusion, the present study iden
[3]
and Use of Laboratory Animals (23). The DCM mouse model was established by intraperitoneal injection
order_basis
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f2132e96ae6c7a4e
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:32626989", "kind": "science-record", "revision": 7, "content_hash": "sha256:9ec3072b6865c23855d293d97c8c76e2d3d94badca7a498fc2fc9685404908d2", "created_at": "2026-11-01T15:41:05Z", "updated_at": "2026-11-01T22:01:52Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Integrated microarray analysis to identify potential biomarkers and therapeutic targets in dilated cardiomyopathy.", "doi": "10.3892/mmr.2020.11145", "pmid": "32626989", "authors": ["Hao Zhang", "Junyu Huo", "Wanying Jiang", "Qijun Shan"], "journal": "Molecular medicine reports", "year": 2020, "abstract": "Dilated cardiomyopathy (DCM) is a primary cardiomyopathy with high mortality. The aim of the present study was to identify the related genes in DCM. The four expression profiles (GSE17800, GSE21610, GSE42955 and GSE79962) downloaded from the Gene Expression Omnibus (GEO) database were analyzed using RankProd and metaMA R packages to identify differentially expressed genes (DEGs). DEGs were uploaded to the Database for Annotation, Visualization and Integrated Discovery (DAVID), for Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis. A protein‑protein interaction (PPI) network of the DEGs was constructed using the STRING database. In addition, hub genes were identified using the Cytoscape plugin cytoHubba. A mouse DCM model, which established via intraperitoneal injection with doxorubicin (DOX), was used to validate the hub genes. A total of 898 DEGs were identified across the four microarrays. Furthermore, GO analysis demonstrated that these DEGs were mainly enriched in cell adhesion, negative regulation of cell proliferation, negative regulation of apoptotic process and potassium ion transport. In addition, KEGG analysis revealed that DEGs were mainly enriched in the ECM‑receptor interaction, the p53 signaling pathway, cardiac muscle contraction and the hypoxia‑inducible factor signaling pathway. Proenkephalin (PENK), chordin like 1 (CHRDL1), calumenin (CALU), apolipoprotein L1, insulin‑like growth factor binding protein 3 (IGFBP3) and ceruloplasmin (CP) were identified as hub genes in the PPI network. Furthermore, the expression levels of PENK, CHRDL1, IGFBP3, CP and CALU in hearts with DCM were validated using a mouse model. In conclusion, the present study identified six hub genes related to DCM. 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