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In vivo demonstration of an active tumor pretargeting approach with peptide nucleic acid bioconjugates as complementary system
A novel, promising strategy for cancer diagnosis and therapy is the use of a pretargeting approach. For this purpose, the non-natural DNA/RNA analogues Peptide Nucleic Acids (PNAs) are ideal candidates as in vivo recognition units due to their high metabolic stability and lack of unspecific accumula...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5949856/ https://www.ncbi.nlm.nih.gov/pubmed/29861898 http://dx.doi.org/10.1039/c5sc00951k |
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author | Leonidova, Anna Foerster, Christian Zarschler, Kristof Schubert, Maik Pietzsch, Hans-Jürgen Steinbach, Jörg Bergmann, Ralf Metzler-Nolte, Nils Stephan, Holger Gasser, Gilles |
author_facet | Leonidova, Anna Foerster, Christian Zarschler, Kristof Schubert, Maik Pietzsch, Hans-Jürgen Steinbach, Jörg Bergmann, Ralf Metzler-Nolte, Nils Stephan, Holger Gasser, Gilles |
author_sort | Leonidova, Anna |
collection | PubMed |
description | A novel, promising strategy for cancer diagnosis and therapy is the use of a pretargeting approach. For this purpose, the non-natural DNA/RNA analogues Peptide Nucleic Acids (PNAs) are ideal candidates as in vivo recognition units due to their high metabolic stability and lack of unspecific accumulation. In the pretargeting approach, an unlabeled, highly specific antibody–PNA conjugate has sufficient time to target a tumor before administration of a small fast-clearing radiolabeled complementary PNA that hybridizes with the antibody–PNA conjugate at the tumor site. Herein, we report the first successful application of this multistep process using a PNA-modified epidermal growth factor receptor (EGFR) specific antibody (cetuximab) and a complementary (99m)Tc-labeled PNA. In vivo studies on tumor bearing mice demonstrated a rapid and efficient in vivo hybridization of the radiolabeled PNA with the antibody–PNA conjugate. Decisively, a high specific tumor accumulation was observed with a tumor-to-muscle ratio of >8, resulting in a clear visualization of the tumor by single photon emission computed tomography (SPECT). |
format | Online Article Text |
id | pubmed-5949856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-59498562018-06-01 In vivo demonstration of an active tumor pretargeting approach with peptide nucleic acid bioconjugates as complementary system Leonidova, Anna Foerster, Christian Zarschler, Kristof Schubert, Maik Pietzsch, Hans-Jürgen Steinbach, Jörg Bergmann, Ralf Metzler-Nolte, Nils Stephan, Holger Gasser, Gilles Chem Sci Chemistry A novel, promising strategy for cancer diagnosis and therapy is the use of a pretargeting approach. For this purpose, the non-natural DNA/RNA analogues Peptide Nucleic Acids (PNAs) are ideal candidates as in vivo recognition units due to their high metabolic stability and lack of unspecific accumulation. In the pretargeting approach, an unlabeled, highly specific antibody–PNA conjugate has sufficient time to target a tumor before administration of a small fast-clearing radiolabeled complementary PNA that hybridizes with the antibody–PNA conjugate at the tumor site. Herein, we report the first successful application of this multistep process using a PNA-modified epidermal growth factor receptor (EGFR) specific antibody (cetuximab) and a complementary (99m)Tc-labeled PNA. In vivo studies on tumor bearing mice demonstrated a rapid and efficient in vivo hybridization of the radiolabeled PNA with the antibody–PNA conjugate. Decisively, a high specific tumor accumulation was observed with a tumor-to-muscle ratio of >8, resulting in a clear visualization of the tumor by single photon emission computed tomography (SPECT). Royal Society of Chemistry 2015-10-01 2015-06-17 /pmc/articles/PMC5949856/ /pubmed/29861898 http://dx.doi.org/10.1039/c5sc00951k Text en This journal is © The Royal Society of Chemistry 2015 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Leonidova, Anna Foerster, Christian Zarschler, Kristof Schubert, Maik Pietzsch, Hans-Jürgen Steinbach, Jörg Bergmann, Ralf Metzler-Nolte, Nils Stephan, Holger Gasser, Gilles In vivo demonstration of an active tumor pretargeting approach with peptide nucleic acid bioconjugates as complementary system |
title |
In vivo demonstration of an active tumor pretargeting approach with peptide nucleic acid bioconjugates as complementary system
|
title_full |
In vivo demonstration of an active tumor pretargeting approach with peptide nucleic acid bioconjugates as complementary system
|
title_fullStr |
In vivo demonstration of an active tumor pretargeting approach with peptide nucleic acid bioconjugates as complementary system
|
title_full_unstemmed |
In vivo demonstration of an active tumor pretargeting approach with peptide nucleic acid bioconjugates as complementary system
|
title_short |
In vivo demonstration of an active tumor pretargeting approach with peptide nucleic acid bioconjugates as complementary system
|
title_sort | in vivo demonstration of an active tumor pretargeting approach with peptide nucleic acid bioconjugates as complementary system |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5949856/ https://www.ncbi.nlm.nih.gov/pubmed/29861898 http://dx.doi.org/10.1039/c5sc00951k |
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