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Molecular imaging of a cancer-targeting theragnostics probe using a nucleolin aptamer- and microRNA-221 molecular beacon-conjugated nanoparticle

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dc.contributor.authorKim, Jin Kyeoung-
dc.contributor.authorChoi, Kyung-Ju-
dc.contributor.authorLee, Minhyung-
dc.contributor.authorJo, Mi-hee-
dc.contributor.authorKim, Soonhag-
dc.date.accessioned2022-07-16T17:00:45Z-
dc.date.available2022-07-16T17:00:45Z-
dc.date.created2021-05-12-
dc.date.issued2012-01-
dc.identifier.issn0142-9612-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/166479-
dc.description.abstractMicroRNAs (miRNA, miR) have been reported as cancer biomarkers that regulate tumor suppressor genes. Hence, simultaneous detecting and inhibiting of miRNA function will be useful as a cancer theragnostics probe to minimize side effects and invasiveness. In this study, we developed a cancer-targeting therangostics probe in a single system using an AS1411 aptamer - and miRNA-221 molecular beacon (miR-221 MB)-conjugated magnetic fluorescence (MF) nanoparticle (MFAS miR-221 MB) to simultaneously target to cancer tissue, image intracellularly expressed miRNA-221 and treat miRNA-221-involved carcinogenesis. AS1411 aptamer-conjugated MF (MFAS) nanoparticles displayed a great selectivity and delivery into various cancer cell lines. The miR-221 MB detached from the MFAS miR-221 MB in the cytoplasm of C6 cells clearly imaged miRNA-221 biogenesis and simultaneously resulted in antitumor therapeutic effects by inhibiting miRNA function, indicating a successful astrocytoma-targeting theragnostics. MFAS miRNA MB can be easily applied to other cancers by simply changing a targeted miRNA highly expressed in cancers.-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER SCI LTD-
dc.titleMolecular imaging of a cancer-targeting theragnostics probe using a nucleolin aptamer- and microRNA-221 molecular beacon-conjugated nanoparticle-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Minhyung-
dc.identifier.doi10.1016/j.biomaterials.2011.09.023-
dc.identifier.scopusid2-s2.0-82855175161-
dc.identifier.wosid000297399700021-
dc.identifier.bibliographicCitationBIOMATERIALS, v.33, no.1, pp.207 - 217-
dc.relation.isPartOfBIOMATERIALS-
dc.citation.titleBIOMATERIALS-
dc.citation.volume33-
dc.citation.number1-
dc.citation.startPage207-
dc.citation.endPage217-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.subject.keywordPlusMESSENGER-RNA EXPRESSION-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusQUANTUM DOTS-
dc.subject.keywordPlusKAPPA-B-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusBIOGENESIS-
dc.subject.keywordPlusDELIVERY-
dc.subject.keywordPlusMIRNAS-
dc.subject.keywordPlusSYSTEM-
dc.subject.keywordPlusGENE-
dc.subject.keywordAuthorAptamer-
dc.subject.keywordAuthormicroRNA-221-
dc.subject.keywordAuthorTheragnostics-
dc.subject.keywordAuthorMolecular beacon-
dc.subject.keywordAuthorMultimodal nanoparticles-
dc.subject.keywordAuthorCancer targeting-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0142961211010647?via%3Dihub-
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