Evaluating gene expression patterns for NF-κB1, TNF, and VEGF A& VEGF B in a mouse model of SARS-CoV-2 infection

The coronavirus disease (COVID-19) pandemic has encouraged extensive research into its pathophysiology, specifically the role of biomarkers in disease progression. Although TNF, NF-κB1, VEGF-A, and VEGF-B play fundamental roles in vascular development and the infection response, their precise involvement in COVID-19 remains unclear. We aimed to evaluate and synthesize TNF, NF-κB1, VEGF-A, and VEGF-B gene expression patterns in a mouse model of SARS-CoV-2 infection to understand their involvement in disease pathogenesis. Gene datasets available on the open-source Gene Expression Omnibus (GEO) platform were extracted from eleven specific datasets: GSE68220, GSE51387, GSE49262, GSE51386, GSE50000, GSE40824, GSE33266, GSE50878, GSE40840, GSE49263, and GSE40827. We used R 4.3.2 software in this analysis. A Substantial changes in the expression of VEGFA, VEGFB, TNF-, and NF-κB1 were observed. Upregulation of TNF- and NF-κB1 implies a strong inflammatory response, consistent with their established involvement in inflammation. Conversely, VEGFA and VEGFB showed a pattern of downregulation, suggesting alterations in the vascular and endothelial functions. Substantial changes in TNF, NF-κB1, VEGFA, and VEGFB gene expression were observed During SARS-CoV infection, indicating their interconnected roles in disease pathogenesis. These findings improve our understanding of the molecular basis of COVID-19 vascular complications and will guide future research and therapies. • TNF, NF-KB, VEGF A and B could have a critical role in COVID-19 disease progression and response. • The precise involvement of TNF, NF-KB, (VEGF) A and B in the pathogenesis of COVID-19 remain unclear. • TNF, NF-KB, VEGF-A and VEGF-B gene expression were explored in a mouse model of SARS-CoV-2. • Significant TNF, NF-κB1, VEGFA, and VEGFB genes expressions were demonstrated. • Understanding these molecular Basis may impact future research and therapies.

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Publication Details

Journal
Medicine in Microecology
Published
2025-03-07
DOI
https://doi.org/10.1016/j.medmic.2025.100124
Citations
1
Primary Topic
Virus-based gene therapy research
Type
article
Field-Weighted Citation Impact
1.82
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article

Evaluating gene expression patterns for NF-κB1, TNF, and VEGF A& VEGF B in a mouse model of SARS-CoV-2 infection

Mahmoud Abdelshakour, Iván Chérrez-Ojeda, Feras Al‐Obeidat, Muneir Gador et al.
1 citations
Medicine in Microecology
Virus-based gene therapy research
1.82
article

Evaluating gene expression patterns for NF-κB1, TNF, and VEGF A& VEGF B in a mouse model of SARS-CoV-2 infection

Mahmoud Abdelshakour, Iván Chérrez-Ojeda, Feras Al‐Obeidat, Muneir Gador, Daniel Simancas‐Racines, Wael Hafez, Asrar Rashid, Seema Iqbal, Nouran Hamza, Tesfalidet Emoshe, Antesh Yadav, Samuel Tesfaye Tefera, Farah El-Sadaany, Alaaldeen Mohamed, Sondos A.H. Thuminat, Mohammad Alkammar
article en
1 citations

Abstract

The coronavirus disease (COVID-19) pandemic has encouraged extensive research into its pathophysiology, specifically the role of biomarkers in disease progression. Although TNF, NF-κB1, VEGF-A, and VEGF-B play fundamental roles in vascular development and the infection response, their precise involvement in COVID-19 remains unclear. We aimed to evaluate and synthesize TNF, NF-κB1, VEGF-A, and VEGF-B gene expression patterns in a mouse model of SARS-CoV-2 infection to understand their involvement in disease pathogenesis. Gene datasets available on the open-source Gene Expression Omnibus (GEO) platform were extracted from eleven specific datasets: GSE68220, GSE51387, GSE49262, GSE51386, GSE50000, GSE40824, GSE33266, GSE50878, GSE40840, GSE49263, and GSE40827. We used R 4.3.2 software in this analysis. A Substantial changes in the expression of VEGFA, VEGFB, TNF-, and NF-κB1 were observed. Upregulation of TNF- and NF-κB1 implies a strong inflammatory response, consistent with their established involvement in inflammation. Conversely, VEGFA and VEGFB showed a pattern of downregulation, suggesting alterations in the vascular and endothelial functions. Substantial changes in TNF, NF-κB1, VEGFA, and VEGFB gene expression were observed During SARS-CoV infection, indicating their interconnected roles in disease pathogenesis. These findings improve our understanding of the molecular basis of COVID-19 vascular complications and will guide future research and therapies. • TNF, NF-KB, VEGF A and B could have a critical role in COVID-19 disease progression and response. • The precise involvement of TNF, NF-KB, (VEGF) A and B in the pathogenesis of COVID-19 remain unclear. • TNF, NF-KB, VEGF-A and VEGF-B gene expression were explored in a mouse model of SARS-CoV-2. • Significant TNF, NF-κB1, VEGFA, and VEGFB genes expressions were demonstrated. • Understanding these molecular Basis may impact future research and therapies.

Medicine in MicroecologyVol. 24
Al Noor Hospitals (AE), Khyber Medical College (PK), Khyber Medical University (PK), Edinburgh Napier University (GB), Royal Lancaster Infirmary (GB), Shaikh Khalifa Medical City (AE), MODUL University Dubai (AE), Universidad Espíritu Santo (EC), Universidad UTE (EC), Abu Dhabi Health Services (AE), National Research Centre (EG), New York University (US), Zayed University (AE)
Good health and well-being
Openalex Percentile: Top 18%
Virus-based gene therapy research
1.82
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