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pmid:37026010

Identification of common molecular signatures of SARS-CoV-2 infection and its influence on acute kidney injury and chronic kidney disease.

Weiwei Zhang · Leping Liu · Xiangcheng Xiao · Hongshan Zhou · Zhangzhe Peng · Wei Wang · Ling Huang · Yanyun Xie · Hui Xu · Lijian Tao · Wannian Nie · Xiangning Yuan · Fang Liu · Qiongjing Yuan

Frontiers in immunology · 2023 doi:10.3389/fimmu.2023.961642

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

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:37026010
kind
science-record
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sha256:635b5d6553869711b68cb461c31c278d206a372c231e153c13ab515eebddc818
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https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json
created_at
2026-11-01T19:01:41Z
updated_at
2026-11-01T22:51:39Z
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paper object · 10 fields
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title
Identification of common molecular signatures of SARS-CoV-2 infection and its influence on acute kidney injury and chronic kidney disease.
doi
10.3389/fimmu.2023.961642
pmid
37026010
authors array · 14 items
[0]
Weiwei Zhang
[1]
Leping Liu
[2]
Xiangcheng Xiao
[3]
Hongshan Zhou
[4]
Zhangzhe Peng
[5]
Wei Wang
[6]
Ling Huang
[7]
Yanyun Xie
[8]
Hui Xu
[9]
Lijian Tao
[10]
Wannian Nie
[11]
Xiangning Yuan
[12]
Fang Liu
[13]
Qiongjing Yuan
journal
Frontiers in immunology
year
2023
abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the main cause of COVID-19, causing hundreds of millions of confirmed cases and more than 18.2 million deaths worldwide. Acute kidney injury (AKI) is a common complication of COVID-19 that leads to an increase in mortality, especially in intensive care unit (ICU) settings, and chronic kidney disease (CKD) is a high risk factor for COVID-19 and its related mortality. However, the underlying molecular mechanisms among AKI, CKD, and COVID-19 are unclear. Therefore, transcriptome analysis was performed to examine common pathways and molecular biomarkers for AKI, CKD, and COVID-19 in an attempt to understand the association of SARS-CoV-2 infection with AKI and CKD. Three RNA-seq datasets (GSE147507, GSE1563, and GSE66494) from the GEO database were used to detect differentially expressed genes (DEGs) for COVID-19 with AKI and CKD to search for shared pathways and candidate targets. A total of 17 common DEGs were confirmed, and their biological functions and signaling pathways were characterized by enrichment analysis. MAPK signaling, the structural pathway of interleukin 1 (IL-1), and the Toll-like receptor pathway appear to be involved in the occurrence of these diseases. Hub genes identified from the protein-protein interaction (PPI) network, including DUSP6, BHLHE40, RASGRP1, and TAB2, are potential therapeutic targets in COVID-19 with AKI and CKD. Common genes and pathways may play pathogenic roles in these three diseases mainly through the activation of immune inflammation. Networks of transcription factor (TF)-gene, miRNA-gene, and gene-disease interactions from the datasets were also constructed, and key gene regulators influencing the progression of these three diseases were further identified among the DEGs. Moreover, new drug targets were predicted based on these common DEGs, and molecular docking and molecular dynamics (MD) simulations were performed. Finally, a diagnostic model of COVID-19 was established based on these common DEGs. Taken together, the molecular and signaling pathways identified in this study may be related to the mechanisms by which SARS-CoV-2 infection affects renal function. These findings are significant for the effective treatment of COVID-19 in patients with kidney diseases.
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/ Supplementary Material .
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sections[26] "Data availability statement" paragraph 2
quote
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/ Supplementary Material .
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This integrated analysis identified 17 DEGs that are common to SARS-CoV-2, AKI, and CKD.
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qualitative
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sections[16] "Identification of DEGs and common DEGs among COVID-19, AKI, and CKD" paragraph 3
quote
This integrated analysis identified 17 DEGs that are common to SARS-CoV-2, AKI, and CKD.
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This integrated analysis identified 17 DEGs that are common to SARS-CoV-2, AKI, and CKD.
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the published estimate and its evidence
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https://doi.org/10.3389/fimmu.2023.961642
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/ Supplementary Material .
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/ Supplementary Material .
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GSM4462400
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GSM4486165
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110
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null
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null
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18573;28369
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Mustela putorius furo; Homo sapiens
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Transcriptional response to SARS-CoV-2 infection
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2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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[2] object · 15 fields
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data:geo:GSE1563
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE1563
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GSE1563
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null
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/ Supplementary Material .
structure object · 15 fields
repository
GEO
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GEO accession URL
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/ Supplementary Material .
access_statement_kind
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GSM26805
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GSM26807
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GSM26809
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GSM26810
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GSM26812
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GSM26813
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GSM26814
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GSM26816
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GSM26817
[13]
GSM26818
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GSM26819
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GSM26820
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GSM26821
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GSM26823
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GSM26824
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GSM26825
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GSM26828
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GSM26830
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GSM26831
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GSM26832
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GSM26833
[29]
GSM26834
[30]
GSM26835
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GSM26836
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GSM26837
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GSM26839
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GSM26840
[36]
GSM26841
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GSM26842
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GSM26843
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GSM26844
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GSM26845
[41]
GSM26846
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GSM26851
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GSM26853
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[52]
GSM26857
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GSM26861
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GSM26864
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GSM26865
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GSM26866
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62
group_sizes
null
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null
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8300
taxon
Homo sapiens
title
Kidney Transplant Rejection and Tissue Injury by Gene Profiling of Biopsies and Peripheral Blood Lymphocytes
resolution_checked_at
2026-11-01T18:46:34Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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[3] object · 15 fields
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data:geo:GSE66494
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null
note
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/ Supplementary Material .
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GEO
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GEO accession URL
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/ Supplementary Material .
access_statement_kind
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61
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null
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null
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6480
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Homo sapiens
title
Development of gene expression profiles in human chronic kidney disease
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2026-11-01T18:06:44Z
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identifier_resolution_only_no_download_no_licence_read
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[0]
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[3]
asset:data:geo:GSE1563 licence not read
[4]
asset:data:geo:GSE66494 not downloaded
[5]
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method-1
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quote
DEGs for the acquired datasets GSE147507, GSE1563, and GSE66494 were first identified from long expression values with the LIMMA package and Benjamini–Hochberg calibration to control for the false discovery rate and DESeq2 in the R programming language (v 4.0.2) for multiple test options.
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count_matrix_with_condition
evidence object · 3 fields
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0.8
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evidence object · 3 fields
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evidence object · 3 fields
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protein-protein interaction
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/ Supplementary Material .
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SARS-CoV-2 infection with AKI and CKD. Three RNA-seq datasets (GSE147507, GSE1563, and GSE66494)
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I, CKD, and COVID-19 are unclear. Therefore, transcriptome analysis was performed to examine common pat
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DEGs for the acquired datasets GSE147507, GSE1563, and GSE66494 were first identified from long expression values with the LIMMA package and Benjamini–Hochberg calibration to control for the false discovery rate and DESeq2 in the R programming language (v 4.0.2) for multiple test options.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37026010", "kind": "science-record", "revision": 4, "content_hash": "sha256:635b5d6553869711b68cb461c31c278d206a372c231e153c13ab515eebddc818", "created_at": "2026-11-01T19:01:41Z", "updated_at": "2026-11-01T22:51:39Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of common molecular signatures of SARS-CoV-2 infection and its influence on acute kidney injury and chronic kidney disease.", "doi": "10.3389/fimmu.2023.961642", "pmid": "37026010", "authors": ["Weiwei Zhang", "Leping Liu", "Xiangcheng Xiao", "Hongshan Zhou", "Zhangzhe Peng", "Wei Wang", "Ling Huang", "Yanyun Xie", "Hui Xu", "Lijian Tao", "Wannian Nie", "Xiangning Yuan", "Fang Liu", "Qiongjing Yuan"], "journal": "Frontiers in immunology", "year": 2023, "abstract": "Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the main cause of COVID-19, causing hundreds of millions of confirmed cases and more than 18.2 million deaths worldwide. Acute kidney injury (AKI) is a common complication of COVID-19 that leads to an increase in mortality, especially in intensive care unit (ICU) settings, and chronic kidney disease (CKD) is a high risk factor for COVID-19 and its related mortality. However, the underlying molecular mechanisms among AKI, CKD, and COVID-19 are unclear. Therefore, transcriptome analysis was performed to examine common pathways and molecular biomarkers for AKI, CKD, and COVID-19 in an attempt to understand the association of SARS-CoV-2 infection with AKI and CKD. Three RNA-seq datasets (GSE147507, GSE1563, and GSE66494) from the GEO database were used to detect differentially expressed genes (DEGs) for COVID-19 with AKI and CKD to search for shared pathways and candidate targets. A total of 17 common DEGs were confirmed, and their biological functions and signaling pathways were characterized by enrichment analysis. MAPK signaling, the structural pathway of interleukin 1 (IL-1), and the Toll-like receptor pathway appear to be involved in the occurrence of these diseases. Hub genes identified from the protein-protein interaction (PPI) network, including DUSP6, BHLHE40, RASGRP1, and TAB2, are potential therapeutic targets in COVID-19 with AKI and CKD. Common genes and pathways may play pathogenic roles in these three diseases mainly through the activation of immune inflammation. Networks of transcription factor (TF)-gene, miRNA-gene, and gene-disease interactions from the datasets were also constructed, and key gene regulators influencing the progression of these three diseases were further identified among the DEGs. Moreover, new drug targets were predicted based on these common DEGs, and molecular docking and molecular dynamics (MD) simulations were performed. Finally, a diagnostic model of COVID-19 was established based on these common DEGs. 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Three RNA-seq datasets (GSE147507, GSE1563, and GSE66494)", "I, CKD, and COVID-19 are unclear. Therefore, transcriptome analysis was performed to examine common pat"], "order_basis": "paper_text_order:625", "id": "assay:1"}, {"role": "analysis", "definition_id": "differential_expression", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": ["normalise_counts", "differential_expression_fit", "fdr_bh"], "support_state": "supported", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 1.0, "evidence": ["DEGs for the acquired datasets GSE147507, GSE1563, and GSE66494 were first identified from long expression values with the LIMMA package and Benjamini–Hochberg calibration to control for the false discovery rate and DESeq2 in the R programming language (v 4.0.2) for multiple test options."], "order_basis": "consumes_earlier_output", "id": "assay:2"}]}