» Articles » PMID: 33301755

Targeting Host DEAD-box RNA Helicase DDX3X for Treating Viral Infections

Overview
Journal Antiviral Res
Publisher Elsevier
Date 2020 Dec 10
PMID 33301755
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

DDX3X or DDX3, a member of the DEAD (asp, glu, ala, asp) box RNA helicase family of proteins, is a multifunctional protein, which is usurped by several viruses and is vital to their production. To date, 18 species of virus from 12 genera have been demonstrated to be dependent on DDX3 for virulence. In addition, DDX3 has been shown to function within 7 of 10 subcellular regions that are involved in the metabolism of viruses. As such, due to its direct interaction with viral components across most or all stages of viral life cycles, DDX3 can be considered an excellent host target for pan-antiviral drug therapy and has been reported to be a possible broad-spectrum antiviral target. Along these lines, it has been demonstrated that treatment of virally infected cells with small molecule inhibitors of DDX3 blunts virion productions. On the other hand, DDX3 bolsters an innate immune response and viruses have evolved capacities to sequester or block DDX3, which dampens an innate immune response. Thus, enhancing DDX3 production or co-targeting direct viral products that interfere with DDX3's modulation of innate immunity would also diminish virion production. Here we review the evidence that supports the hypothesis that modulating DDX3's agonistic and antagonistic functions during viral infections could have an important impact on safely and efficiently subduing a broad-spectrum of viral infections.

Citing Articles

DDX RNA helicases: key players in cellular homeostasis and innate antiviral immunity.

Tapescu I, Cherry S J Virol. 2024; 98(10):e0004024.

PMID: 39212449 PMC: 11494928. DOI: 10.1128/jvi.00040-24.


RNA-RNA interactions between respiratory syncytial virus and miR-26 and miR-27 are associated with regulation of cell cycle and antiviral immunity.

Ressel S, Kumar S, Bermudez-Barrientos J, Gordon K, Lane J, Wu J Nucleic Acids Res. 2024; 52(9):4872-4888.

PMID: 38412296 PMC: 11109944. DOI: 10.1093/nar/gkae116.


The Viral Protein K7 Inhibits Biochemical Activities and Condensate Formation by the DEAD-box Helicase DDX3X.

Venus S, Tandjigora K, Jankowsky E J Mol Biol. 2023; 435(19):168217.

PMID: 37517790 PMC: 10528715. DOI: 10.1016/j.jmb.2023.168217.


The RNA helicase DDX3 and its role in c-MYC driven germinal center-derived B-cell lymphoma.

Lacroix M, Beauchemin H, Khandanpour C, Moroy T Front Oncol. 2023; 13:1148936.

PMID: 37035206 PMC: 10081492. DOI: 10.3389/fonc.2023.1148936.


DDX3X Is Hijacked by Snakehead Vesiculovirus Phosphoprotein To Facilitate Virus Replication via Stabilization of the Phosphoprotein.

Bei C, Zhang C, Wu H, Feng H, Zhang Y, Tu J J Virol. 2023; 97(2):e0003523.

PMID: 36744958 PMC: 9972964. DOI: 10.1128/jvi.00035-23.


References
1.
Megahed F, Zhou X, Sun P . The Interactions between HBV and the Innate Immunity of Hepatocytes. Viruses. 2020; 12(3). PMC: 7150781. DOI: 10.3390/v12030285. View

2.
Riva V, Maga G . From the magic bullet to the magic target: exploiting the diverse roles of DDX3X in viral infections and tumorigenesis. Future Med Chem. 2019; 11(11):1357-1381. DOI: 10.4155/fmc-2018-0451. View

3.
Xu L, Khadijah S, Fang S, Wang L, Tay F, Liu D . The cellular RNA helicase DDX1 interacts with coronavirus nonstructural protein 14 and enhances viral replication. J Virol. 2010; 84(17):8571-83. PMC: 2918985. DOI: 10.1128/JVI.00392-10. View

4.
Yang D, Leibowitz J . The structure and functions of coronavirus genomic 3' and 5' ends. Virus Res. 2015; 206:120-33. PMC: 4476908. DOI: 10.1016/j.virusres.2015.02.025. View

5.
Brai A, Riva V, Saladini F, Zamperini C, Trivisani C, Garbelli A . DDX3X inhibitors, an effective way to overcome HIV-1 resistance targeting host proteins. Eur J Med Chem. 2020; 200:112319. DOI: 10.1016/j.ejmech.2020.112319. View