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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 |
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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.
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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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[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.</description><identifier>ISSN: 2372-7705</identifier><identifier>EISSN: 2372-7705</identifier><identifier>DOI: 10.1016/j.omto.2021.10.011</identifier><language>eng</language><publisher>Elsevier Inc</publisher><subject>DNA nanoparticle ; EGFR-targeting ; GBM ; gene therapy ; glioblastoma ; NIS ; polyplexes ; radioiodine ; sodium iodide symporter</subject><ispartof>Molecular therapy. Oncolytics, 2021-12, Vol.23, p.432-446</ispartof><rights>2021 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c340t-8986bec0b0cda2fd5d8cc5f84e6a87b662e91e36f99921ec567eb2fa7f222d073</citedby><cites>FETCH-LOGICAL-c340t-8986bec0b0cda2fd5d8cc5f84e6a87b662e91e36f99921ec567eb2fa7f222d073</cites><orcidid>0000-0001-5239-4628 ; 0000-0002-3572-7205 ; 0000-0001-8413-0934 ; 0000-0003-2680-5715 ; 0000-0002-0413-9697 ; 0000-0002-6837-9104 ; 0000-0002-1258-2584</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S2372770521001480$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,777,781,3536,27905,27906,45761</link.rule.ids></links><search><creatorcontrib>Spellerberg, Rebekka</creatorcontrib><creatorcontrib>Benli-Hoppe, Teoman</creatorcontrib><creatorcontrib>Kitzberger, Carolin</creatorcontrib><creatorcontrib>Berger, Simone</creatorcontrib><creatorcontrib>Schmohl, Kathrin A.</creatorcontrib><creatorcontrib>Schwenk, Nathalie</creatorcontrib><creatorcontrib>Yen, Hsi-Yu</creatorcontrib><creatorcontrib>Zach, Christian</creatorcontrib><creatorcontrib>Schilling, Franz</creatorcontrib><creatorcontrib>Weber, Wolfgang A.</creatorcontrib><creatorcontrib>Kälin, Roland E.</creatorcontrib><creatorcontrib>Glass, Rainer</creatorcontrib><creatorcontrib>Nelson, Peter J.</creatorcontrib><creatorcontrib>Wagner, Ernst</creatorcontrib><creatorcontrib>Spitzweg, Christine</creatorcontrib><title>Selective sodium iodide symporter (NIS) gene therapy of glioblastoma mediated by EGFR-targeted lipopolyplexes</title><title>Molecular therapy. Oncolytics</title><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.</description><subject>DNA nanoparticle</subject><subject>EGFR-targeting</subject><subject>GBM</subject><subject>gene therapy</subject><subject>glioblastoma</subject><subject>NIS</subject><subject>polyplexes</subject><subject>radioiodine</subject><subject>sodium iodide symporter</subject><issn>2372-7705</issn><issn>2372-7705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kMFq3DAQhk1poCHNC_SkY3vwRhqvZRl6KSFJF0ILTXoWI2m01WJHRlJD_fbVZkvpqafR_PB_jL6meSf4RnAhrw6bOJe4AQ6iBhsuxKvmHLoB2mHg_et_3m-ay5wPnHOxlWrsu_NmfqCJbAnPxHJ04efMQh2ubuu8xFQosfdfdg8f2J6eiJUflHBZWfRsP4VoJswlzshmcgELOWZWdnN3-60tmPZ0DKawxCVO6zLRL8pvmzOPU6bLP_Oi-X5783j9ub3_ere7_nTf2m7LS6tGJQ1Zbrh1CN71Tlnbe7UliWowUgKNgjrpx3EEQbaXAxnwOHgAcHzoLprdiesiHvSSwoxp1RGDfgli2mtMJdiJNIJAIBpAjbTtnVESPEejwPdorJCVBSeWTTHnRP4vT3B99K8rsPrXR__HrPqvpY-nEtVfPgdKOttAT7Z6SlV3PSP8r_4b_TeQlQ</recordid><startdate>20211217</startdate><enddate>20211217</enddate><creator>Spellerberg, Rebekka</creator><creator>Benli-Hoppe, Teoman</creator><creator>Kitzberger, Carolin</creator><creator>Berger, Simone</creator><creator>Schmohl, Kathrin A.</creator><creator>Schwenk, Nathalie</creator><creator>Yen, Hsi-Yu</creator><creator>Zach, Christian</creator><creator>Schilling, Franz</creator><creator>Weber, Wolfgang A.</creator><creator>Kälin, Roland E.</creator><creator>Glass, Rainer</creator><creator>Nelson, Peter J.</creator><creator>Wagner, Ernst</creator><creator>Spitzweg, Christine</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-5239-4628</orcidid><orcidid>https://orcid.org/0000-0002-3572-7205</orcidid><orcidid>https://orcid.org/0000-0001-8413-0934</orcidid><orcidid>https://orcid.org/0000-0003-2680-5715</orcidid><orcidid>https://orcid.org/0000-0002-0413-9697</orcidid><orcidid>https://orcid.org/0000-0002-6837-9104</orcidid><orcidid>https://orcid.org/0000-0002-1258-2584</orcidid></search><sort><creationdate>20211217</creationdate><title>Selective sodium iodide symporter (NIS) gene therapy of glioblastoma mediated by EGFR-targeted lipopolyplexes</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-8986bec0b0cda2fd5d8cc5f84e6a87b662e91e36f99921ec567eb2fa7f222d073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>DNA nanoparticle</topic><topic>EGFR-targeting</topic><topic>GBM</topic><topic>gene therapy</topic><topic>glioblastoma</topic><topic>NIS</topic><topic>polyplexes</topic><topic>radioiodine</topic><topic>sodium iodide symporter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Spellerberg, Rebekka</creatorcontrib><creatorcontrib>Benli-Hoppe, Teoman</creatorcontrib><creatorcontrib>Kitzberger, Carolin</creatorcontrib><creatorcontrib>Berger, Simone</creatorcontrib><creatorcontrib>Schmohl, Kathrin A.</creatorcontrib><creatorcontrib>Schwenk, Nathalie</creatorcontrib><creatorcontrib>Yen, Hsi-Yu</creatorcontrib><creatorcontrib>Zach, Christian</creatorcontrib><creatorcontrib>Schilling, Franz</creatorcontrib><creatorcontrib>Weber, Wolfgang A.</creatorcontrib><creatorcontrib>Kälin, Roland E.</creatorcontrib><creatorcontrib>Glass, Rainer</creatorcontrib><creatorcontrib>Nelson, Peter J.</creatorcontrib><creatorcontrib>Wagner, Ernst</creatorcontrib><creatorcontrib>Spitzweg, Christine</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>CrossRef</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Molecular therapy. Oncolytics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Spellerberg, Rebekka</au><au>Benli-Hoppe, Teoman</au><au>Kitzberger, Carolin</au><au>Berger, Simone</au><au>Schmohl, Kathrin A.</au><au>Schwenk, Nathalie</au><au>Yen, Hsi-Yu</au><au>Zach, Christian</au><au>Schilling, Franz</au><au>Weber, Wolfgang A.</au><au>Kälin, Roland E.</au><au>Glass, Rainer</au><au>Nelson, Peter J.</au><au>Wagner, Ernst</au><au>Spitzweg, Christine</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Selective sodium iodide symporter (NIS) gene therapy of glioblastoma mediated by EGFR-targeted lipopolyplexes</atitle><jtitle>Molecular therapy. Oncolytics</jtitle><date>2021-12-17</date><risdate>2021</risdate><volume>23</volume><spage>432</spage><epage>446</epage><pages>432-446</pages><issn>2372-7705</issn><eissn>2372-7705</eissn><abstract>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.</abstract><pub>Elsevier Inc</pub><doi>10.1016/j.omto.2021.10.011</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0001-5239-4628</orcidid><orcidid>https://orcid.org/0000-0002-3572-7205</orcidid><orcidid>https://orcid.org/0000-0001-8413-0934</orcidid><orcidid>https://orcid.org/0000-0003-2680-5715</orcidid><orcidid>https://orcid.org/0000-0002-0413-9697</orcidid><orcidid>https://orcid.org/0000-0002-6837-9104</orcidid><orcidid>https://orcid.org/0000-0002-1258-2584</orcidid><oa>free_for_read</oa></addata></record> |
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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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