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pmid:33897765

Identification of Hub Genes and Construction of a Transcriptional Regulatory Network Associated With Tumor Recurrence in Colorectal Cancer by Weighted Gene Co-expression Network Analysis.

Shengwei Liu · Fanping Zeng · Guangwen Fan · Qiyong Dong

Frontiers in genetics · 2021 doi:10.3389/fgene.2021.649752

Paper

complete

Experiment

complete

Data

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Analysis

complete

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title
Identification of Hub Genes and Construction of a Transcriptional Regulatory Network Associated With Tumor Recurrence in Colorectal Cancer by Weighted Gene Co-expression Network Analysis.
doi
10.3389/fgene.2021.649752
pmid
33897765
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[0]
Shengwei Liu
[1]
Fanping Zeng
[2]
Guangwen Fan
[3]
Qiyong Dong
journal
Frontiers in genetics
year
2021
abstract
Tumor recurrence is one of the most important risk factors that can negatively affect the survival rate of colorectal cancer (CRC) patients. However, the key regulators dictating this process and their exact mechanisms are understudied. This study aimed to construct a gene co-expression network to predict the hub genes affecting CRC recurrence and to inspect the regulatory network of hub genes and transcription factors (TFs). A total of 177 cases from the GSE17536 dataset were analyzed via weighted gene co-expression network analysis to explore the modules related to CRC recurrence. Functional annotation of the key module genes was assessed through Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analyses. The protein and protein interaction network was then built to screen hub genes. Samples from the Cancer Genome Atlas (TCGA) were further used to validate the hub genes. Construction of a TFs-miRNAs-hub genes network was also conducted using StarBase and Cytoscape approaches. After identification and validation, a total of five genes (TIMP1, SPARCL1, MYL9, TPM2, and CNN1) were selected as hub genes. A regulatory network of TFs-miRNAs-targets with 29 TFs, 58 miRNAs, and five hub genes was instituted, including model GATA6-MIR106A-CNN1, SP4-MIR424-TPM2, SP4-MIR326-MYL9, ETS1-MIR22-TIMP1, and ETS1-MIR22-SPARCL1. In conclusion, the identification of these hub genes and the prediction of the Regulatory relationship of TFs-miRNAs-hub genes may provide a novel insight for understanding the underlying mechanism for CRC recurrence.
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GS was calculated by linear regression between gene expression and CRC recurrence, and MS related to clinical CRC recurrence was obtained.
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GS was calculated by linear regression between gene expression and CRC recurrence, and MS related to clinical CRC recurrence was obtained.
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Metastasis Gene Expression Profile Predicts Recurrence and Death in Colon Cancer Patients (Moffitt Samples)
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Summary of top 10 regulatory biomolecules (TFs and miRNAs) of the five hub genes in CRC identified from TFs-miRNAs-hub genes interactions.
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Construction of TFs-miRNA–Hub Genes Network Associated With CRC Recurrence
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Summary of top 10 regulatory biomolecules (TFs and miRNAs) of the five hub genes in CRC identified from TFs-miRNAs-hub genes interactions.
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snapshot_id
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lineage object · 4 fields
parent_id
pmid:33897765
parent_hash
sha256:c6b24e1a3c69751cc2cb996cf368744a8f7e199d6e0a0f51dfc53a75f13a225f
fork_of
null
gaps array · 6 items
[0]
asset:data:geo:GSE17536 licence not read
[1]
asset:data:geo:GSE17536 not downloaded
[2]
execution.not_run
[3]
review.human_critique
[4]
review.independent_reader
[5]
review.machine_critique
assays array · 1 item
[0] object · 11 fields
role
analysis
definition_id
regression_modelling
definition_version
f2132e96ae6c7a4e
required_operations array · 1 item
[0]
ols_fit
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
GS was calculated by linear regression between gene expression and CRC recurrence, and MS related to clinical CRC recurrence was obtained.
order_basis
analysis_only
id
assay:1
Complete file
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However, the key regulators dictating this process and their exact mechanisms are understudied. This study aimed to construct a gene co-expression network to predict the hub genes affecting CRC recurrence and to inspect the regulatory network of hub genes and transcription factors (TFs). A total of 177 cases from the GSE17536 dataset were analyzed via weighted gene co-expression network analysis to explore the modules related to CRC recurrence. Functional annotation of the key module genes was assessed through Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analyses. The protein and protein interaction network was then built to screen hub genes. Samples from the Cancer Genome Atlas (TCGA) were further used to validate the hub genes. Construction of a TFs-miRNAs-hub genes network was also conducted using StarBase and Cytoscape approaches. After identification and validation, a total of five genes (TIMP1, SPARCL1, MYL9, TPM2, and CNN1) were selected as hub genes. A regulatory network of TFs-miRNAs-targets with 29 TFs, 58 miRNAs, and five hub genes was instituted, including model GATA6-MIR106A-CNN1, SP4-MIR424-TPM2, SP4-MIR326-MYL9, ETS1-MIR22-TIMP1, and ETS1-MIR22-SPARCL1. 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