» Articles » PMID: 33238570

The Potential Role of Osteopontin and Furin in Worsening Disease Outcomes in COVID-19 Patients with Pre-Existing Diabetes

Overview
Journal Cells
Publisher MDPI
Date 2020 Nov 26
PMID 33238570
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

The novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused the ongoing coronavirus disease 2019 (COVID-19) pandemic, with more than 50 million cases reported globally. Findings have consistently identified an increased severity of SARS-CoV-2 infection in individuals with diabetes. Osteopontin, a cytokine-like matrix-associated phosphoglycoprotein, is elevated in diabetes and drives the expression of furin, a proprotein convertase implicated in the proteolytic processing and activation of several precursors, including chemokines, growth factors, hormones, adhesion molecules, and receptors. Elevated serum furin is a signature of diabetes mellitus progression and is associated with a dysmetabolic phenotype and increased risk of diabetes-linked premature mortality. Additionally, furin plays an important role in enhancing the infectivity of SARS-CoV-2 by promoting its entry and replication in the host cell. Here, we hypothesize that diabetes-induced osteopontin and furin protein upregulation results in worse outcomes in diabetic patients with SARS-CoV-2 infection owing to the roles of these protein in promoting viral infection and increasing metabolic dysfunction. Thus, targeting the osteopontin-furin axis may be a plausible strategy for reducing mortality in SARS-CoV-2 patients with diabetes.

Citing Articles

Potential Effects of Hyperglycemia on SARS-CoV-2 Entry Mechanisms in Pancreatic Beta Cells.

Michaels T, Essop M, Joseph D Viruses. 2024; 16(8).

PMID: 39205219 PMC: 11358987. DOI: 10.3390/v16081243.


The Role of Osteopontin in Respiratory Health and Disease.

Barkas G, Kotsiou O J Pers Med. 2023; 13(8).

PMID: 37623509 PMC: 10455105. DOI: 10.3390/jpm13081259.


Organokines in COVID-19: A Systematic Review.

Barbalho S, Minniti G, Miola V, Dos Santos Haber J, Cincotto Dos Santos Bueno P, Santos de Argollo Haber L Cells. 2023; 12(10).

PMID: 37408184 PMC: 10216619. DOI: 10.3390/cells12101349.


The Intracellular and Secreted Sides of Osteopontin and Their Putative Physiopathological Roles.

Bastos A, Gomes A, Silva G, Emerenciano M, Ferreira L, Gimba E Int J Mol Sci. 2023; 24(3).

PMID: 36769264 PMC: 9917417. DOI: 10.3390/ijms24032942.


Understanding Molecular Actors of SARS-CoV-2 Virulence to Tackle COVID-19 Outbreak.

Berisio R Cells. 2022; 11(22).

PMID: 36429024 PMC: 9688472. DOI: 10.3390/cells11223597.


References
1.
Cen Y, Chen X, Shen Y, Zhang X, Lei Y, Xu C . Risk factors for disease progression in patients with mild to moderate coronavirus disease 2019-a multi-centre observational study. Clin Microbiol Infect. 2020; 26(9):1242-1247. PMC: 7280135. DOI: 10.1016/j.cmi.2020.05.041. View

2.
Paniri A, Hosseini M, Akhavan-Niaki H . First comprehensive computational analysis of functional consequences of SNPs in susceptibility to SARS-CoV-2 among different populations. J Biomol Struct Dyn. 2020; 39(10):3576-3593. PMC: 7284145. DOI: 10.1080/07391102.2020.1767690. View

3.
Bader M . Role of the local renin-angiotensin system in cardiac damage: a minireview focussing on transgenic animal models. J Mol Cell Cardiol. 2002; 34(11):1455-62. DOI: 10.1006/jmcc.2002.2077. View

4.
Li Q, Wu J, Nie J, Zhang L, Hao H, Liu S . The Impact of Mutations in SARS-CoV-2 Spike on Viral Infectivity and Antigenicity. Cell. 2020; 182(5):1284-1294.e9. PMC: 7366990. DOI: 10.1016/j.cell.2020.07.012. View

5.
Hoffmann M, Kleine-Weber H, Schroeder S, Kruger N, Herrler T, Erichsen S . SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor. Cell. 2020; 181(2):271-280.e8. PMC: 7102627. DOI: 10.1016/j.cell.2020.02.052. View