<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lee Y</submitter><funding>Ministry of Science, ICT and Future Planning</funding><funding>National Research Foundation of Korea</funding><pagination>249-260</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10658310</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>53</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>miRNA-21 (miR-21) is highly expressed in glioblastoma, facilitating tumor growth by blocking the expression of apoptosis-related genes. Therefore, an antisense microRNA oligonucleotide (AMO) against miR-21 was suggested as a therapeutic nucleic acid for glioblastoma.&lt;h4>Objectives&lt;/h4>AMO21 co-micelles were developed with tumor-targeting T7 peptides as an AMO21 delivery system by intranasal administration.&lt;h4>Methods&lt;/h4>Cholesterol-conjugated AMO21 (AMO21c) was mixed with cholesterol-conjugated T7 peptides (T7c) to produce tumor-targeted co-micelles. Physical characterization was performed by dynamic light scattering, gel retardation assay, scanning electron microscope and heparin competition assay. In vitro transfection efficiency to C6 glioblastoma cells was measure</pubmed_abstract><journal>Journal of advanced research</journal><pubmed_title>Antisense-oligonucleotide co-micelles with tumor targeting peptides elicit therapeutic effects by inhibiting microRNA-21 in the glioblastoma animal models.</pubmed_title><pmcid>PMC10658310</pmcid><funding_grant_id>2022R1A2B5B01001920</funding_grant_id><pubmed_authors>Ha J</pubmed_authors><pubmed_authors>Kang S</pubmed_authors><pubmed_authors>Lee M</pubmed_authors><pubmed_authors>Kang M</pubmed_authors><pubmed_authors>Lee Y</pubmed_authors><pubmed_authors>Kim M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Antisense-oligonucleotide co-micelles with tumor targeting peptides elicit therapeutic effects by inhibiting microRNA-21 in the glioblastoma animal models.</name><description>&lt;h4>Introduction&lt;/h4>miRNA-21 (miR-21) is highly expressed in glioblastoma, facilitating tumor growth by blocking the expression of apoptosis-related genes. Therefore, an antisense microRNA oligonucleotide (AMO) against miR-21 was suggested as a therapeutic nucleic acid for glioblastoma.&lt;h4>Objectives&lt;/h4>AMO21 co-micelles were developed with tumor-targeting T7 peptides as an AMO21 delivery system by intranasal administration.&lt;h4>Methods&lt;/h4>Cholesterol-conjugated AMO21 (AMO21c) was mixed with cholesterol-conjugated T7 peptides (T7c) to produce tumor-targeted co-micelles. Physical characterization was performed by dynamic light scattering, gel retardation assay, scanning electron microscope and heparin competition assay. In vitro transfection efficiency to C6 glioblastoma cells was measure</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Nov</publication><modification>2025-04-22T09:27:08.434Z</modification><creation>2025-04-05T23:03:08.93Z</creation></dates><accession>S-EPMC10658310</accession><cross_references><pubmed>36632887</pubmed><doi>10.1016/j.jare.2023.01.005</doi></cross_references></HashMap>