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Viral G-quadruplexes: New frontiers in virus pathogenesis and antiviral therapy

Viruses are the most abundant organisms on our planet, affecting all living beings: some of them are responsible for massive epidemics that concern health, national economies and the overall welfare of societies. Although advances in antiviral research have led to successful therapies against severa...

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Autores principales: Ruggiero, Emanuela, Richter, Sara N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7233243/
https://www.ncbi.nlm.nih.gov/pubmed/32427223
http://dx.doi.org/10.1016/bs.armc.2020.04.001
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author Ruggiero, Emanuela
Richter, Sara N.
author_facet Ruggiero, Emanuela
Richter, Sara N.
author_sort Ruggiero, Emanuela
collection PubMed
description Viruses are the most abundant organisms on our planet, affecting all living beings: some of them are responsible for massive epidemics that concern health, national economies and the overall welfare of societies. Although advances in antiviral research have led to successful therapies against several human viruses, still some of them cannot be eradicated from the host and most of them do not have any treatment available. Consequently, innovative antiviral therapies are urgently needed. In the past few years, research on G-quadruplexes (G4s) in viruses has boomed, providing powerful evidence for the regulatory role of G4s in key viral steps. Comprehensive bioinformatics analyses have traced putative G4-forming sequences in the genome of almost all human viruses, showing that their distribution is statistically significant and their presence highly conserved. Since the genomes of viruses are remarkably variable, high conservation rates strongly suggest a crucial role of G4s in the viral replication cycle and evolution, emphasizing the possibility of targeting viral G4s as a new pharmacological approach in antiviral therapy. Recent studies have demonstrated the formation and function of G4s in pathogens responsible for serious diseases, such as HIV-1, Hepatitis B and C, Ebola viruses, to cite a few. In this chapter, we present the state of the art on the structural and functional characterization of viral G4s in RNA viruses, DNA viruses and retroviruses. We also present the G4 ligands that provide further details on the viral G4 role and which, showing promising antiviral activity, which could be exploited for the development of innovative antiviral agents.
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spelling pubmed-72332432020-05-18 Viral G-quadruplexes: New frontiers in virus pathogenesis and antiviral therapy Ruggiero, Emanuela Richter, Sara N. Annu Rep Med Chem Article Viruses are the most abundant organisms on our planet, affecting all living beings: some of them are responsible for massive epidemics that concern health, national economies and the overall welfare of societies. Although advances in antiviral research have led to successful therapies against several human viruses, still some of them cannot be eradicated from the host and most of them do not have any treatment available. Consequently, innovative antiviral therapies are urgently needed. In the past few years, research on G-quadruplexes (G4s) in viruses has boomed, providing powerful evidence for the regulatory role of G4s in key viral steps. Comprehensive bioinformatics analyses have traced putative G4-forming sequences in the genome of almost all human viruses, showing that their distribution is statistically significant and their presence highly conserved. Since the genomes of viruses are remarkably variable, high conservation rates strongly suggest a crucial role of G4s in the viral replication cycle and evolution, emphasizing the possibility of targeting viral G4s as a new pharmacological approach in antiviral therapy. Recent studies have demonstrated the formation and function of G4s in pathogens responsible for serious diseases, such as HIV-1, Hepatitis B and C, Ebola viruses, to cite a few. In this chapter, we present the state of the art on the structural and functional characterization of viral G4s in RNA viruses, DNA viruses and retroviruses. We also present the G4 ligands that provide further details on the viral G4 role and which, showing promising antiviral activity, which could be exploited for the development of innovative antiviral agents. Elsevier Inc. 2020 2020-05-18 /pmc/articles/PMC7233243/ /pubmed/32427223 http://dx.doi.org/10.1016/bs.armc.2020.04.001 Text en Copyright © 2020 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Ruggiero, Emanuela
Richter, Sara N.
Viral G-quadruplexes: New frontiers in virus pathogenesis and antiviral therapy
title Viral G-quadruplexes: New frontiers in virus pathogenesis and antiviral therapy
title_full Viral G-quadruplexes: New frontiers in virus pathogenesis and antiviral therapy
title_fullStr Viral G-quadruplexes: New frontiers in virus pathogenesis and antiviral therapy
title_full_unstemmed Viral G-quadruplexes: New frontiers in virus pathogenesis and antiviral therapy
title_short Viral G-quadruplexes: New frontiers in virus pathogenesis and antiviral therapy
title_sort viral g-quadruplexes: new frontiers in virus pathogenesis and antiviral therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7233243/
https://www.ncbi.nlm.nih.gov/pubmed/32427223
http://dx.doi.org/10.1016/bs.armc.2020.04.001
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