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Modulation of Immunosuppression by Oligonucleotide-Based Molecules and Small Molecules Targeting Myeloid-Derived Suppressor Cells

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dc.contributor.authorLim, Jihyun-
dc.contributor.authorLee, Aram-
dc.contributor.authorLee, Hee Gu-
dc.contributor.authorLim, Jong-Seok-
dc.date.available2021-02-22T05:35:50Z-
dc.date.issued2020-01-
dc.identifier.issn1976-9148-
dc.identifier.issn2005-4483-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/2553-
dc.description.abstractMyeloid-derived suppressor cells (MDSCs) are immature myeloid cells that exert suppressive function on the immune response. MDSCs expand in tumor-bearing hosts or in the tumor microenvironment and suppress T cell responses via various mechanisms, whereas a reduction in their activities has been observed in autoimmune diseases or infections. It has been reported that the symptoms of various diseases, including malignant tumors, can be alleviated by targeting MDSCs. Moreover, MDSCs can contribute to patient resistance to therapy using immune checkpoint inhibitors. In line with these therapeutic approaches, diverse oligonucleotide-based molecules and small molecules have been evaluated for their therapeutic efficacy in several disease models via the modulation of MDSC activity. In the current review, MDSC-targeting oligonucleotides and small molecules are briefly summarized, and we highlight the immunomodulatory effects on MDSCs in a variety of disease models and the application of MDSC-targeting molecules for immuno-oncologic therapy.-
dc.format.extent17-
dc.language영어-
dc.language.isoENG-
dc.publisherKOREAN SOC APPLIED PHARMACOLOGY-
dc.titleModulation of Immunosuppression by Oligonucleotide-Based Molecules and Small Molecules Targeting Myeloid-Derived Suppressor Cells-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.4062/biomolther.2019.069-
dc.identifier.scopusid2-s2.0-85078247444-
dc.identifier.wosid000504658700001-
dc.identifier.bibliographicCitationBIOMOLECULES & THERAPEUTICS, v.28, no.1, pp 1 - 17-
dc.citation.titleBIOMOLECULES & THERAPEUTICS-
dc.citation.volume28-
dc.citation.number1-
dc.citation.startPage1-
dc.citation.endPage17-
dc.type.docTypeReview-
dc.identifier.kciidART002536130-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusRECEPTOR TYROSINE KINASES-
dc.subject.keywordPlusENDOTHELIAL GROWTH-FACTOR-
dc.subject.keywordPlusTRANS-RETINOIC ACID-
dc.subject.keywordPlusTUMOR-GROWTH-
dc.subject.keywordPlusSELECTIVE INHIBITOR-
dc.subject.keywordPlusANTITUMOR IMMUNITY-
dc.subject.keywordPlusSIGNAL TRANSDUCER-
dc.subject.keywordPlusPROTEIN-KINASE-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusT-CELLS-
dc.subject.keywordAuthorMyeloid-derived suppressor cells (MDSCs)-
dc.subject.keywordAuthorOligonucleotide-based molecules-
dc.subject.keywordAuthorSmall molecules-
dc.subject.keywordAuthorTumor microenvironment-
dc.subject.keywordAuthorImmune suppression-
dc.subject.keywordAuthorMDSC-targeting agents-
dc.identifier.urlhttp://www.biomolther.org/journal/view.html?volume=28&number=1&spage=1&year=2020-
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