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Metastatic and non-metastatic melanoma imaging using Sgc8-c aptamer PTK7-recognizer

Melanoma is one of the most aggressive and deadly skin cancers, and although histopathological criteria are used for its prognosis, biomarkers are necessary to identify the different evolution stages. The applications of molecular imaging include the in vivo diagnosis of cancer with probes that reco...

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Autores principales: Sicco, Estefanía, Mónaco, Amy, Fernandez, Marcelo, Moreno, María, Calzada, Victoria, Cerecetto, Hugo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497559/
https://www.ncbi.nlm.nih.gov/pubmed/34620894
http://dx.doi.org/10.1038/s41598-021-98828-6
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author Sicco, Estefanía
Mónaco, Amy
Fernandez, Marcelo
Moreno, María
Calzada, Victoria
Cerecetto, Hugo
author_facet Sicco, Estefanía
Mónaco, Amy
Fernandez, Marcelo
Moreno, María
Calzada, Victoria
Cerecetto, Hugo
author_sort Sicco, Estefanía
collection PubMed
description Melanoma is one of the most aggressive and deadly skin cancers, and although histopathological criteria are used for its prognosis, biomarkers are necessary to identify the different evolution stages. The applications of molecular imaging include the in vivo diagnosis of cancer with probes that recognize the tumor-biomarkers specific expression allowing external image acquisitions and evaluation of the biological process in quali-quantitative ways. Aptamers are oligonucleotides that recognize targets with high affinity and specificity presenting advantages that make them interesting molecular imaging probes. Sgc8-c (DNA-aptamer) selectively recognizes PTK7-receptor overexpressed in various types of tumors. Herein, Sgc8-c was evaluated, for the first time, in a metastatic melanoma model as molecular imaging probe for in vivo diagnostic, as well as in a non-metastatic melanoma model. Firstly, two probes, radio- and fluorescent-probe, were in vitro evaluated verifying the high specific PTK7 recognition and its internalization in tumor cells by the endosomal route. Secondly, in vivo proof of concept was performed in animal tumor models. In addition, they have rapid clearance from blood exhibiting excellent target (tumor)/non-target organ ratios. Furthermore, optimal biodistribution was observed 24 h after probes injections accumulating almost exclusively in the tumor tissue. Sgc8-c is a potential tool for their specific use in the early detection of melanoma.
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spelling pubmed-84975592021-10-12 Metastatic and non-metastatic melanoma imaging using Sgc8-c aptamer PTK7-recognizer Sicco, Estefanía Mónaco, Amy Fernandez, Marcelo Moreno, María Calzada, Victoria Cerecetto, Hugo Sci Rep Article Melanoma is one of the most aggressive and deadly skin cancers, and although histopathological criteria are used for its prognosis, biomarkers are necessary to identify the different evolution stages. The applications of molecular imaging include the in vivo diagnosis of cancer with probes that recognize the tumor-biomarkers specific expression allowing external image acquisitions and evaluation of the biological process in quali-quantitative ways. Aptamers are oligonucleotides that recognize targets with high affinity and specificity presenting advantages that make them interesting molecular imaging probes. Sgc8-c (DNA-aptamer) selectively recognizes PTK7-receptor overexpressed in various types of tumors. Herein, Sgc8-c was evaluated, for the first time, in a metastatic melanoma model as molecular imaging probe for in vivo diagnostic, as well as in a non-metastatic melanoma model. Firstly, two probes, radio- and fluorescent-probe, were in vitro evaluated verifying the high specific PTK7 recognition and its internalization in tumor cells by the endosomal route. Secondly, in vivo proof of concept was performed in animal tumor models. In addition, they have rapid clearance from blood exhibiting excellent target (tumor)/non-target organ ratios. Furthermore, optimal biodistribution was observed 24 h after probes injections accumulating almost exclusively in the tumor tissue. Sgc8-c is a potential tool for their specific use in the early detection of melanoma. Nature Publishing Group UK 2021-10-07 /pmc/articles/PMC8497559/ /pubmed/34620894 http://dx.doi.org/10.1038/s41598-021-98828-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Sicco, Estefanía
Mónaco, Amy
Fernandez, Marcelo
Moreno, María
Calzada, Victoria
Cerecetto, Hugo
Metastatic and non-metastatic melanoma imaging using Sgc8-c aptamer PTK7-recognizer
title Metastatic and non-metastatic melanoma imaging using Sgc8-c aptamer PTK7-recognizer
title_full Metastatic and non-metastatic melanoma imaging using Sgc8-c aptamer PTK7-recognizer
title_fullStr Metastatic and non-metastatic melanoma imaging using Sgc8-c aptamer PTK7-recognizer
title_full_unstemmed Metastatic and non-metastatic melanoma imaging using Sgc8-c aptamer PTK7-recognizer
title_short Metastatic and non-metastatic melanoma imaging using Sgc8-c aptamer PTK7-recognizer
title_sort metastatic and non-metastatic melanoma imaging using sgc8-c aptamer ptk7-recognizer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497559/
https://www.ncbi.nlm.nih.gov/pubmed/34620894
http://dx.doi.org/10.1038/s41598-021-98828-6
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