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pmid:38932215

Identification and Analysis of Biomarkers Associated with Lipophagy and Therapeutic Agents for COVID-19.

Yujia Wu · Zhenlin Wu · Qiying Jin · Jinyuan Liu · Peiping Xu

Viruses · 2024 doi:10.3390/v16060923

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:38932215
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science-record
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sha256:35139e709d3bef89b88c4bdc71d34f054e25b70912ef0d55fa29808a3eb259ff
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2026-11-01T20:29:00Z
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2026-11-01T22:54:35Z
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title
Identification and Analysis of Biomarkers Associated with Lipophagy and Therapeutic Agents for COVID-19.
doi
10.3390/v16060923
pmid
38932215
authors array · 5 items
[0]
Yujia Wu
[1]
Zhenlin Wu
[2]
Qiying Jin
[3]
Jinyuan Liu
[4]
Peiping Xu
journal
Viruses
year
2024
abstract
BACKGROUND: Lipids, as a fundamental cell component, play an regulating role in controlling the different cellular biological processes involved in viral infections. A notable feature of coronavirus disease 2019 (COVID-19) is impaired lipid metabolism. The function of lipophagy-related genes in COVID-19 is unknown. The present study aimed to investigate biomarkers and drug targets associated with lipophagy and lipophagy-based therapeutic agents for COVID-19 through bioinformatics analysis. METHODS: Lipophagy-related biomarkers for COVID-19 were identified using machine learning algorithms such as random forest, Support Vector Machine-Recursive Feature Elimination, Generalized Linear Model, and Extreme Gradient Boosting in three COVID-19-associated GEO datasets: scRNA-seq (GSE145926) and bulk RNA-seq (GSE183533 and GSE190496). The cMAP database was searched for potential COVID-19 medications. RESULTS: The lipophagy pathway was downregulated, and the lipid droplet formation pathway was upregulated, resulting in impaired lipid metabolism. Seven lipophagy-related genes, including ACADVL, HYOU1, DAP, AUP1, PRXAB2, LSS, and PLIN2, were used as biomarkers and drug targets for COVID-19. Moreover, lipophagy may play a role in COVID-19 pathogenesis. As prospective drugs for treating COVID-19, seven potential downregulators (phenoxybenzamine, helveticoside, lanatoside C, geldanamycin, loperamide, pioglitazone, and trichostatin A) were discovered. These medication candidates showed remarkable binding energies against the seven biomarkers. CONCLUSIONS: The lipophagy-related genes ACADVL, HYOU1, DAP, AUP1, PRXAB2, LSS, and PLIN2 can be used as biomarkers and drug targets for COVID-19. Seven potential downregulators of these seven biomarkers may have therapeutic effects for treating COVID-19.
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DEGs between COVID-19 patients and the control group derived from the scRNA cells and RNAseq were identified using the DEG analysis in Seurat and the edgeR package in R, respectively.
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sections[5] "2.3. Identification of Differentially Expressed Genes (DEGs)" paragraph 2
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DEGs between COVID-19 patients and the control group derived from the scRNA cells and RNAseq were identified using the DEG analysis in Seurat and the edgeR package in R, respectively.
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sections[30] "Data Availability Statement" paragraph 2
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All data generated or analyzed during this study are included in this article/Supplementary Materials.
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Seven lipophagy-related genes, including ACADVL, HYOU1, DAP, AUP1, PRXAB2, LSS, and PLIN2, were used as biomarkers and drug targets for COVID-19.
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sections[0] "Abstract" paragraph 1
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Seven lipophagy-related genes, including ACADVL, HYOU1, DAP, AUP1, PRXAB2, LSS, and PLIN2, were used as biomarkers and drug targets for COVID-19.
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Seven lipophagy-related genes, including ACADVL, HYOU1, DAP, AUP1, PRXAB2, LSS, and PLIN2, were used as biomarkers and drug targets for COVID-19.
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DEGs between COVID-19 patients and the control group derived from the scRNA cells and RNAseq were identified using the DEG analysis in Seurat and the edgeR package in R, respectively.
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:38932215", "kind": "science-record", "revision": 4, "content_hash": "sha256:35139e709d3bef89b88c4bdc71d34f054e25b70912ef0d55fa29808a3eb259ff", "created_at": "2026-11-01T20:29:00Z", "updated_at": "2026-11-01T22:54:35Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification and Analysis of Biomarkers Associated with Lipophagy and Therapeutic Agents for COVID-19.", "doi": "10.3390/v16060923", "pmid": "38932215", "authors": ["Yujia Wu", "Zhenlin Wu", "Qiying Jin", "Jinyuan Liu", "Peiping Xu"], "journal": "Viruses", "year": 2024, "abstract": "BACKGROUND: Lipids, as a fundamental cell component, play an regulating role in controlling the different cellular biological processes involved in viral infections. A notable feature of coronavirus disease 2019 (COVID-19) is impaired lipid metabolism. The function of lipophagy-related genes in COVID-19 is unknown. The present study aimed to investigate biomarkers and drug targets associated with lipophagy and lipophagy-based therapeutic agents for COVID-19 through bioinformatics analysis.\nMETHODS: Lipophagy-related biomarkers for COVID-19 were identified using machine learning algorithms such as random forest, Support Vector Machine-Recursive Feature Elimination, Generalized Linear Model, and Extreme Gradient Boosting in three COVID-19-associated GEO datasets: scRNA-seq (GSE145926) and bulk RNA-seq (GSE183533 and GSE190496). The cMAP database was searched for potential COVID-19 medications.\nRESULTS: The lipophagy pathway was downregulated, and the lipid droplet formation pathway was upregulated, resulting in impaired lipid metabolism. Seven lipophagy-related genes, including ACADVL, HYOU1, DAP, AUP1, PRXAB2, LSS, and PLIN2, were used as biomarkers and drug targets for COVID-19. Moreover, lipophagy may play a role in COVID-19 pathogenesis. As prospective drugs for treating COVID-19, seven potential downregulators (phenoxybenzamine, helveticoside, lanatoside C, geldanamycin, loperamide, pioglitazone, and trichostatin A) were discovered. These medication candidates showed remarkable binding energies against the seven biomarkers.\nCONCLUSIONS: The lipophagy-related genes ACADVL, HYOU1, DAP, AUP1, PRXAB2, LSS, and PLIN2 can be used as biomarkers and drug targets for COVID-19. Seven potential downregulators of these seven biomarkers may have therapeutic effects for treating COVID-19.", "claims": [{"id": "claim-method", "statement": "DEGs between COVID-19 patients and the control group derived from the scRNA cells and RNAseq were identified using the DEG analysis in Seurat and the edgeR package in R, respectively.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38932215", "locator": "sections[5] \"2.3. 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