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Selective sodium iodide symporter (NIS) gene therapy of glioblastoma mediated by EGFR-targeted lipopolyplexes

Lipo-oligomers, post-functionalized with ligands to enhance targeting, represent promising new vehicles for the tumor-specific delivery of therapeutic genes such as the sodium iodide symporter (NIS). Due to its iodide trapping activity, NIS is a powerful theranostic tool for diagnostic imaging and t...

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Published in:Molecular therapy. Oncolytics 2021-12, Vol.23, p.432-446
Main Authors: Spellerberg, Rebekka, Benli-Hoppe, Teoman, Kitzberger, Carolin, Berger, Simone, Schmohl, Kathrin A., Schwenk, Nathalie, Yen, Hsi-Yu, Zach, Christian, Schilling, Franz, Weber, Wolfgang A., Kälin, Roland E., Glass, Rainer, Nelson, Peter J., Wagner, Ernst, Spitzweg, Christine
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cited_by cdi_FETCH-LOGICAL-c340t-8986bec0b0cda2fd5d8cc5f84e6a87b662e91e36f99921ec567eb2fa7f222d073
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container_title Molecular therapy. Oncolytics
container_volume 23
creator Spellerberg, Rebekka
Benli-Hoppe, Teoman
Kitzberger, Carolin
Berger, Simone
Schmohl, Kathrin A.
Schwenk, Nathalie
Yen, Hsi-Yu
Zach, Christian
Schilling, Franz
Weber, Wolfgang A.
Kälin, Roland E.
Glass, Rainer
Nelson, Peter J.
Wagner, Ernst
Spitzweg, Christine
description Lipo-oligomers, post-functionalized with ligands to enhance targeting, represent promising new vehicles for the tumor-specific delivery of therapeutic genes such as the sodium iodide symporter (NIS). Due to its iodide trapping activity, NIS is a powerful theranostic tool for diagnostic imaging and the application of therapeutic radionuclides. 124I PET imaging allows non-invasive monitoring of the in vivo biodistribution of functional NIS expression, and application of 131I enables cytoreduction. In our experimental design, we used epidermal growth factor receptor (EGFR)-targeted polyplexes (GE11) initially characterized in vitro using 125I uptake assays. Mice bearing an orthotopic glioblastoma were treated subsequently with mono-dibenzocyclooctyne (DBCO)-PEG24-GE11/NIS or bisDBCO-PEG24-GE11/NIS, and 24–48 h later, 124I uptake was assessed by positron emission tomography (PET) imaging. The best-performing polyplex in the imaging studies was then selected for 131I therapy studies. The in vitro studies showed EGFR-dependent and NIS-specific transfection efficiency of the polyplexes. The injection of monoDBCO-PEG24-GE11/NIS polyplexes 48 h before 124I application was characterized to be the optimal regime in the imaging studies and was therefore used for an 131I therapy study, showing a significant decrease in tumor growth and a significant extension of survival in the therapy group. These studies demonstrate the potential of EGFR-targeted polyplex-mediated NIS gene therapy as a new strategy for the therapy of glioblastoma. [Display omitted] EGFR-targeted lipopolyplexes represent promising new vehicles for the tumor-specific delivery of therapeutic genes, such as the theranostic sodium iodide symporter (NIS). Spellerberg et al. established specific and highly efficient polyplexes for an effective NIS gene therapy concept of glioblastoma.
doi_str_mv 10.1016/j.omto.2021.10.011
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source Open Access: PubMed Central; ScienceDirect Journals
subjects DNA nanoparticle
EGFR-targeting
GBM
gene therapy
glioblastoma
NIS
polyplexes
radioiodine
sodium iodide symporter
title Selective sodium iodide symporter (NIS) gene therapy of glioblastoma mediated by EGFR-targeted lipopolyplexes
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