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Aptamer-based Targeted Delivery of a G-quadruplex Ligand in Cervical Cancer Cells

AS1411 is a G-rich DNA oligonucleotide that functions as an aptamer of the protein nucleolin, found at high levels on the surface of cancer cells but not on the surface of normal cells. Herein, we have studied AS1411 as a supramolecular carrier for the delivery of an acridine-based G-quadruplex liga...

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Autores principales: Carvalho, Josué, Paiva, Artur, Cabral Campello, Maria Paula, Paulo, António, Mergny, Jean-Louis, Salgado, Gilmar F., Queiroz, João A., Cruz, Carla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6538641/
https://www.ncbi.nlm.nih.gov/pubmed/31138870
http://dx.doi.org/10.1038/s41598-019-44388-9
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author Carvalho, Josué
Paiva, Artur
Cabral Campello, Maria Paula
Paulo, António
Mergny, Jean-Louis
Salgado, Gilmar F.
Queiroz, João A.
Cruz, Carla
author_facet Carvalho, Josué
Paiva, Artur
Cabral Campello, Maria Paula
Paulo, António
Mergny, Jean-Louis
Salgado, Gilmar F.
Queiroz, João A.
Cruz, Carla
author_sort Carvalho, Josué
collection PubMed
description AS1411 is a G-rich DNA oligonucleotide that functions as an aptamer of the protein nucleolin, found at high levels on the surface of cancer cells but not on the surface of normal cells. Herein, we have studied AS1411 as a supramolecular carrier for the delivery of an acridine-based G-quadruplex ligand, C(8), to HeLa cancer cells. Two AS1411 derivatives, LNA-AS1411 and U-AS1411, were also tested, in an attempt to compare AS1411 pharmacological properties. The results showed that AS1411-C(8) complexation was made with great binding strength and that it lowered the ligand’s cytotoxicity towards non-malignant cells. This effect was suggested to be due to a decreased internalization of the complexed versus free C(8) as shown by flow cytometry. The AS1411 derivatives, despite forming a stable complex with C(8), lacked the necessary tumour-selective behaviour. The binding of C(8) to AS1411 G-quadruplex structure did not negatively affect the recognition of nucleolin by the aptamer. The AS1411-C(8) repressed c-MYC expression at the transcriptional level, possibly due to C(8) ability to stabilize the c-MYC promoter G-quadruplexes. Overall, this study demonstrates the usefulness of AS1411 as a supramolecular carrier of the G-quadruplex binder C(8) and the potential of using its tumour-selective properties for the delivery of ligands for cancer therapy.
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spelling pubmed-65386412019-06-06 Aptamer-based Targeted Delivery of a G-quadruplex Ligand in Cervical Cancer Cells Carvalho, Josué Paiva, Artur Cabral Campello, Maria Paula Paulo, António Mergny, Jean-Louis Salgado, Gilmar F. Queiroz, João A. Cruz, Carla Sci Rep Article AS1411 is a G-rich DNA oligonucleotide that functions as an aptamer of the protein nucleolin, found at high levels on the surface of cancer cells but not on the surface of normal cells. Herein, we have studied AS1411 as a supramolecular carrier for the delivery of an acridine-based G-quadruplex ligand, C(8), to HeLa cancer cells. Two AS1411 derivatives, LNA-AS1411 and U-AS1411, were also tested, in an attempt to compare AS1411 pharmacological properties. The results showed that AS1411-C(8) complexation was made with great binding strength and that it lowered the ligand’s cytotoxicity towards non-malignant cells. This effect was suggested to be due to a decreased internalization of the complexed versus free C(8) as shown by flow cytometry. The AS1411 derivatives, despite forming a stable complex with C(8), lacked the necessary tumour-selective behaviour. The binding of C(8) to AS1411 G-quadruplex structure did not negatively affect the recognition of nucleolin by the aptamer. The AS1411-C(8) repressed c-MYC expression at the transcriptional level, possibly due to C(8) ability to stabilize the c-MYC promoter G-quadruplexes. Overall, this study demonstrates the usefulness of AS1411 as a supramolecular carrier of the G-quadruplex binder C(8) and the potential of using its tumour-selective properties for the delivery of ligands for cancer therapy. Nature Publishing Group UK 2019-05-28 /pmc/articles/PMC6538641/ /pubmed/31138870 http://dx.doi.org/10.1038/s41598-019-44388-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Carvalho, Josué
Paiva, Artur
Cabral Campello, Maria Paula
Paulo, António
Mergny, Jean-Louis
Salgado, Gilmar F.
Queiroz, João A.
Cruz, Carla
Aptamer-based Targeted Delivery of a G-quadruplex Ligand in Cervical Cancer Cells
title Aptamer-based Targeted Delivery of a G-quadruplex Ligand in Cervical Cancer Cells
title_full Aptamer-based Targeted Delivery of a G-quadruplex Ligand in Cervical Cancer Cells
title_fullStr Aptamer-based Targeted Delivery of a G-quadruplex Ligand in Cervical Cancer Cells
title_full_unstemmed Aptamer-based Targeted Delivery of a G-quadruplex Ligand in Cervical Cancer Cells
title_short Aptamer-based Targeted Delivery of a G-quadruplex Ligand in Cervical Cancer Cells
title_sort aptamer-based targeted delivery of a g-quadruplex ligand in cervical cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6538641/
https://www.ncbi.nlm.nih.gov/pubmed/31138870
http://dx.doi.org/10.1038/s41598-019-44388-9
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