Journal article

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, B Tang, A McLean, M Shojaei

International Journal of Molecular Sciences | MDPI | Published : 2023

Abstract

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 colle..

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University of Melbourne Researchers

Grants

Awarded by National Institute of Allergy and Infectious Diseases


Funding Acknowledgements

This study was funded by Snow Medical Research Foundation (BEAT COVID-19), the National Health and Medical Research Council (Australian Partnership for Preparedness Research on Infectious Disease Emergencies (APPRISE AppID 1116530)), the Jack Ma Foundation, and the A2 Milk Company. This study was also supported by intramural grants from the Helmholtz-Association: intramural funding; University of Tennessee Health Science Center: intramural funding; NIAID: 5U19A|100625-07; NIAID: 2-U19-AI100625-06 awarded to KS. K.R.S. is supported by NHMRC investigator grant 2007919.