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Pathway and Network Analyses Identify Growth Factor Signaling and MMP9 as Potential Mediators of Mitochondrial Dysfunction in Severe COVID-19
Y. Wang, K. Schughart, TM. Pelaia, T. Chew, K. Kim, T. Karvunidis, B. Knippenberg, S. Teoh, AL. Phu, KR. Short, J. Iredell, I. Thevarajan, J. Audsley, S. Macdonald, J. Burcham, . Predict-Consortium, B. Tang, A. McLean, M. Shojaei
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články
Grantová podpora
5U19A|100625-07
NIAID NIH HHS - United States
NLK
Free Medical Journals
od 2000
Freely Accessible Science Journals
od 2000
PubMed Central
od 2007
Europe PubMed Central
od 2007
ProQuest Central
od 2000-03-01
Open Access Digital Library
od 2000-01-01
Open Access Digital Library
od 2007-01-01
Health & Medicine (ProQuest)
od 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
od 2000
PubMed
36768847
DOI
10.3390/ijms24032524
Knihovny.cz E-zdroje
- MeSH
- COVID-19 * MeSH
- lidé MeSH
- matrixová metaloproteinasa 9 genetika metabolismus MeSH
- mezibuněčné signální peptidy a proteiny MeSH
- mitochondrie metabolismus MeSH
- signální transdukce MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
Patients with preexisting metabolic disorders such as diabetes are at a higher risk of developing severe coronavirus disease 2019 (COVID-19). Mitochondrion, the very organelle that controls cellular metabolism, holds the key to understanding disease progression at the cellular level. Our current study aimed to understand how cellular metabolism contributes to COVID-19 outcomes. Metacore pathway enrichment analyses on differentially expressed genes (encoded by both mitochondrial and nuclear deoxyribonucleic acid (DNA)) involved in cellular metabolism, regulation of mitochondrial respiration and organization, and apoptosis, was performed on RNA sequencing (RNASeq) data from blood samples collected from healthy controls and patients with mild/moderate or severe COVID-19. Genes from the enriched pathways were analyzed by network analysis to uncover interactions among them and up- or downstream genes within each pathway. Compared to the mild/moderate COVID-19, the upregulation of a myriad of growth factor and cell cycle signaling pathways, with concomitant downregulation of interferon signaling pathways, were observed in the severe group. Matrix metallopeptidase 9 (MMP9) was found in five of the top 10 upregulated pathways, indicating its potential as therapeutic target against COVID-19. In summary, our data demonstrates aberrant activation of endocrine signaling in severe COVID-19, and its implication in immune and metabolic dysfunction.
Centre for Clinical Research in Emergency Medicine Royal Perth Bentley Group Perth WA 6000 Australia
Department of Intensive Care Medicine Nepean Hospital Kingswood NSW 2747 Australia
Department of Microbiology St George Hospital Sydney NSW 2217 Australia
Emergency Department Royal Perth Hospital Perth WA 6000 Australia
Institute of Virology Münster University of Münster 48149 Münster Germany
Medical School University of Western Australia Perth WA 6009 Australia
Sydney Informatics Hub Core Research Facilities The University of Sydney Sydney NSW 2006 Australia
Sydney Institute for Infectious Disease The University of Sydney Sydney NSW 2145 Australia
Westmead Hospital Western Sydney Local Health District Sydney NSW 2145 Australia
Citace poskytuje Crossref.org
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