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pmid:36466549

Identifying the Effect of COVID-19 Infection in Multiple Myeloma and Diffuse Large B-Cell Lymphoma Patients Using Bioinformatics and System Biology.

Chengcheng Li · Ying Zhang · Yingying Xiao · Yun Luo

Computational and mathematical methods in medicine · 2022 doi:10.1155/2022/7017317

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complete

Experiment

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Data

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:36466549
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title
Identifying the Effect of COVID-19 Infection in Multiple Myeloma and Diffuse Large B-Cell Lymphoma Patients Using Bioinformatics and System Biology.
doi
10.1155/2022/7017317
pmid
36466549
authors array · 4 items
[0]
Chengcheng Li
[1]
Ying Zhang
[2]
Yingying Xiao
[3]
Yun Luo
journal
Computational and mathematical methods in medicine
year
2022
abstract
The severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2), also referred to as COVID-19, has spread to several countries and caused a serious threat to human health worldwide. Patients with confirmed COVID-19 infection spread the disease rapidly throughout the region. Multiple myeloma (MM) and diffuse large B-cell lymphoma (DLBCL) are risk factors for COVID-19, although the molecular mechanisms underlying the relationship among MM, DLBCL, and COVID-19 have not been elucidated so far. In this context, transcriptome analysis was performed in the present study to identify the shared pathways and molecular indicators of MM, DLBCL, and COVID-19, which benefited the overall understanding of the effect of COVID-19 in patients with MM and DLBCL. Three datasets (GSE16558, GSE56315, and GSE152418) were downloaded from the Gene Expression Omnibus (GEO) and searched for the shared differentially expressed genes (DEGs) in patients with MM and DLBCL who were infected with SARS-CoV-2. The objective was to detect similar pathways and prospective medicines. A total of 29 DEGs that were common across these three datasets were selected. A protein-protein interaction (PPI) network was constructed using data from the STRING database followed by the identification of hub genes. In addition, the association of MM and DLBCL with COVID-19 infection was analyzed through functional analysis using ontologies terms and pathway analysis. Three relationships were observed in the evaluated datasets: transcription factor-gene interactions, protein-drug interactions, and an integrated regulatory network of DEGs and miRNAs with mutual DEGs. The findings of the present study revealed potential pharmaceuticals that could be beneficial in the treatment of COVID-19.
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The Linear Models for Microarray Data (LIMMA) package were employed to identify the significant DEGs from the datasets using the criteria of P value < 0.05 and |logFC| ≥ 1.0.
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sections[4] "2.2. Identification of the DEGs and Shared DEGs among MM, DLBCL, and COVID-19" paragraph 2
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The Linear Models for Microarray Data (LIMMA) package were employed to identify the significant DEGs from the datasets using the criteria of P value < 0.05 and |logFC| ≥ 1.0.
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sections[21] "Data Availability" paragraph 2
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Publicly available datasets were analyzed in this study. These data can be found here in National Center for Biotechnology Information (NCBI), Gene Expression Omnibus (GEO), https://www.ncbi.nlm.nih.gov/geo/, GSE152418, GSE16558, and GSE56315.
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A total of 29 DEGs that were common across these three datasets were selected.
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A total of 29 DEGs that were common across these three datasets were selected.
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provenance object · 7 fields
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data:geo:GSE152418
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GEO GSE152418
activities array · 3 items
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type
classification
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pmid:36466549
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PMID 36466549 full text
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data:geo:GSE152418
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dataset
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GEO GSE152418
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agent:corpus-assay-engine
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used array · 1 item
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source:pmid:36466549
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agent:minimax-reader
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activity-resolve-GSE152418
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accession_resolution
used array · 1 item
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agent:corpus-assay-engine
agents array · 2 items
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agent:corpus-assay-engine
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software
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agent:minimax-reader
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software
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dsl_catalogue_fingerprint
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gaps array · 10 items
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[3]
asset:data:geo:GSE16558 not downloaded
[4]
asset:data:geo:GSE56315 licence not read
[5]
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review.human_critique
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review.machine_critique
assays array · 1 item
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source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
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The Linear Models for Microarray Data (LIMMA) package were employed to identify the significant DEGs from the datasets using the criteria of P value < 0.05 and |logFC| ≥ 1.0.
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assay:1
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36466549", "kind": "science-record", "revision": 4, "content_hash": "sha256:6ab4a6026f6f2acaa4294dcb050c450952f1a2077cf9245f0a28d70d7722d23c", "created_at": "2026-11-01T19:00:56Z", "updated_at": "2026-11-01T22:50:44Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identifying the Effect of COVID-19 Infection in Multiple Myeloma and Diffuse Large B-Cell Lymphoma Patients Using Bioinformatics and System Biology.", "doi": "10.1155/2022/7017317", "pmid": "36466549", "authors": ["Chengcheng Li", "Ying Zhang", "Yingying Xiao", "Yun Luo"], "journal": "Computational and mathematical methods in medicine", "year": 2022, "abstract": "The severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2), also referred to as COVID-19, has spread to several countries and caused a serious threat to human health worldwide. Patients with confirmed COVID-19 infection spread the disease rapidly throughout the region. Multiple myeloma (MM) and diffuse large B-cell lymphoma (DLBCL) are risk factors for COVID-19, although the molecular mechanisms underlying the relationship among MM, DLBCL, and COVID-19 have not been elucidated so far. In this context, transcriptome analysis was performed in the present study to identify the shared pathways and molecular indicators of MM, DLBCL, and COVID-19, which benefited the overall understanding of the effect of COVID-19 in patients with MM and DLBCL. Three datasets (GSE16558, GSE56315, and GSE152418) were downloaded from the Gene Expression Omnibus (GEO) and searched for the shared differentially expressed genes (DEGs) in patients with MM and DLBCL who were infected with SARS-CoV-2. The objective was to detect similar pathways and prospective medicines. A total of 29 DEGs that were common across these three datasets were selected. A protein-protein interaction (PPI) network was constructed using data from the STRING database followed by the identification of hub genes. In addition, the association of MM and DLBCL with COVID-19 infection was analyzed through functional analysis using ontologies terms and pathway analysis. Three relationships were observed in the evaluated datasets: transcription factor-gene interactions, protein-drug interactions, and an integrated regulatory network of DEGs and miRNAs with mutual DEGs. The findings of the present study revealed potential pharmaceuticals that could be beneficial in the treatment of COVID-19.", "claims": [{"id": "claim-method", "statement": "The Linear Models for Microarray Data (LIMMA) package were employed to identify the significant DEGs from the datasets using the criteria of P value < 0.05 and |logFC| ≥ 1.0.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36466549", "locator": "sections[4] \"2.2. 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