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The G-quadruplex-forming aptamer AS1411 potently inhibits HIV-1 attachment to the host cell
AS1411 is a G-rich aptamer that forms a stable G-quadruplex structure and displays antineoplastic properties both in vitro and in vivo. This oligonucleotide has undergone phase 2 clinical trials. The major molecular target of AS1411 is nucleolin (NCL), a multifunctional nucleolar protein also presen...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science Publishers
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4840014/ https://www.ncbi.nlm.nih.gov/pubmed/27032748 http://dx.doi.org/10.1016/j.ijantimicag.2016.01.016 |
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author | Perrone, Rosalba Butovskaya, Elena Lago, Sara Garzino-Demo, Alfredo Pannecouque, Christophe Palù, Giorgio Richter, Sara N. |
author_facet | Perrone, Rosalba Butovskaya, Elena Lago, Sara Garzino-Demo, Alfredo Pannecouque, Christophe Palù, Giorgio Richter, Sara N. |
author_sort | Perrone, Rosalba |
collection | PubMed |
description | AS1411 is a G-rich aptamer that forms a stable G-quadruplex structure and displays antineoplastic properties both in vitro and in vivo. This oligonucleotide has undergone phase 2 clinical trials. The major molecular target of AS1411 is nucleolin (NCL), a multifunctional nucleolar protein also present in the cell membrane where it selectively mediates the binding and uptake of AS1411. Cell-surface NCL has been recognised as a low-affinity co-receptor for human immunodeficiency virus type 1 (HIV-1) anchorage on target cells. Here we assessed the anti-HIV-1 properties and underlying mechanism of action of AS1411. The antiviral activity of AS1411 was determined towards different HIV-1 strains, host cells and at various times post-infection. Acutely, persistently and latently infected cells were tested, including HIV-1-infected peripheral blood mononuclear cells from a healthy donor. Mechanistic studies to exclude modes of action other than virus binding via NCL were performed. AS1411 efficiently inhibited HIV-1 attachment/entry into the host cell. The aptamer displayed antiviral activity in the absence of cytotoxicity at the tested doses, therefore displaying a wide therapeutic window and favourable selectivity indexes. These findings, besides validating cell-surface-expressed NCL as an antiviral target, open the way for the possible use of AS1411 as a new potent and promisingly safe anti-HIV-1 agent. |
format | Online Article Text |
id | pubmed-4840014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier Science Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-48400142016-05-02 The G-quadruplex-forming aptamer AS1411 potently inhibits HIV-1 attachment to the host cell Perrone, Rosalba Butovskaya, Elena Lago, Sara Garzino-Demo, Alfredo Pannecouque, Christophe Palù, Giorgio Richter, Sara N. Int J Antimicrob Agents Article AS1411 is a G-rich aptamer that forms a stable G-quadruplex structure and displays antineoplastic properties both in vitro and in vivo. This oligonucleotide has undergone phase 2 clinical trials. The major molecular target of AS1411 is nucleolin (NCL), a multifunctional nucleolar protein also present in the cell membrane where it selectively mediates the binding and uptake of AS1411. Cell-surface NCL has been recognised as a low-affinity co-receptor for human immunodeficiency virus type 1 (HIV-1) anchorage on target cells. Here we assessed the anti-HIV-1 properties and underlying mechanism of action of AS1411. The antiviral activity of AS1411 was determined towards different HIV-1 strains, host cells and at various times post-infection. Acutely, persistently and latently infected cells were tested, including HIV-1-infected peripheral blood mononuclear cells from a healthy donor. Mechanistic studies to exclude modes of action other than virus binding via NCL were performed. AS1411 efficiently inhibited HIV-1 attachment/entry into the host cell. The aptamer displayed antiviral activity in the absence of cytotoxicity at the tested doses, therefore displaying a wide therapeutic window and favourable selectivity indexes. These findings, besides validating cell-surface-expressed NCL as an antiviral target, open the way for the possible use of AS1411 as a new potent and promisingly safe anti-HIV-1 agent. Elsevier Science Publishers 2016-04 /pmc/articles/PMC4840014/ /pubmed/27032748 http://dx.doi.org/10.1016/j.ijantimicag.2016.01.016 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Perrone, Rosalba Butovskaya, Elena Lago, Sara Garzino-Demo, Alfredo Pannecouque, Christophe Palù, Giorgio Richter, Sara N. The G-quadruplex-forming aptamer AS1411 potently inhibits HIV-1 attachment to the host cell |
title | The G-quadruplex-forming aptamer AS1411 potently inhibits HIV-1 attachment to the host cell |
title_full | The G-quadruplex-forming aptamer AS1411 potently inhibits HIV-1 attachment to the host cell |
title_fullStr | The G-quadruplex-forming aptamer AS1411 potently inhibits HIV-1 attachment to the host cell |
title_full_unstemmed | The G-quadruplex-forming aptamer AS1411 potently inhibits HIV-1 attachment to the host cell |
title_short | The G-quadruplex-forming aptamer AS1411 potently inhibits HIV-1 attachment to the host cell |
title_sort | g-quadruplex-forming aptamer as1411 potently inhibits hiv-1 attachment to the host cell |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4840014/ https://www.ncbi.nlm.nih.gov/pubmed/27032748 http://dx.doi.org/10.1016/j.ijantimicag.2016.01.016 |
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