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Cited 27 time in webofscience Cited 28 time in scopus
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The Multifunctional Protein Syntenin-1: Regulator of Exosome Biogenesis, Cellular Function, and Tumor Progression

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dc.contributor.authorLee, Kwang-Min-
dc.contributor.authorSeo, Eun-Chan-
dc.contributor.authorLee, Jeong-Hyung-
dc.contributor.authorKim, Hyo-Jin-
dc.contributor.authorHwangbo, Cheol-
dc.date.accessioned2023-06-22T02:41:29Z-
dc.date.available2023-06-22T02:41:29Z-
dc.date.issued2023-05-
dc.identifier.issn1661-6596-
dc.identifier.issn1422-0067-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/59667-
dc.description.abstractSyntenin acts as an adaptor and scaffold protein through its two PSD-95, Dlg, and ZO-1 (PDZ) domains, participating in multiple signaling pathways and modulating cellular physiology. It has been identified as an oncogene, promoting cancer development, metastasis, and angiogenesis in various carcinomas. Syntenin-1 is also associated with the production and release of exosomes, small extracellular vesicles that play a significant role in intercellular communication by containing bioactive molecules such as proteins, lipids, and nucleic acids. The trafficking of exosomes involves a complex interplay of various regulatory proteins, including syntenin-1, which interacts with its binding partners, syndecan and activated leukocyte cell adhesion molecule (ALIX). Exosomal transfer of microRNAs, a key cargo, can regulate the expression of various cancer-related genes, including syntenin-1. Targeting the mechanism involving the regulation of exosomes by syntenin-1 and microRNAs may provide a novel treatment strategy for cancer. This review highlights the current understanding of syntenin-1’s role in regulating exosome trafficking and its associated cellular signaling pathways. © 2023 by the authors.-
dc.language영어-
dc.language.isoENG-
dc.publisherMDPI-
dc.titleThe Multifunctional Protein Syntenin-1: Regulator of Exosome Biogenesis, Cellular Function, and Tumor Progression-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/ijms24119418-
dc.identifier.scopusid2-s2.0-85161617958-
dc.identifier.wosid001003846100001-
dc.identifier.bibliographicCitationInternational Journal of Molecular Sciences, v.24, no.11-
dc.citation.titleInternational Journal of Molecular Sciences-
dc.citation.volume24-
dc.citation.number11-
dc.type.docTypeReview-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusTO-MESENCHYMAL TRANSITION-
dc.subject.keywordPlusEXTRACELLULAR VESICLES-
dc.subject.keywordPlusINTERCELLULAR-COMMUNICATION-
dc.subject.keywordPlusMULTIVESICULAR BODIES-
dc.subject.keywordPlusPROMOTES METASTASIS-
dc.subject.keywordPlusSIGNALING PATHWAY-
dc.subject.keywordPlusMATRIX ADHESION-
dc.subject.keywordPlusBREAST-CANCER-
dc.subject.keywordPlusPDZ PROTEIN-
dc.subject.keywordPlusSTEM-CELLS-
dc.subject.keywordAuthorexosome-
dc.subject.keywordAuthormicroRNA-
dc.subject.keywordAuthorsyntenin-1-
dc.subject.keywordAuthortrafficking-
dc.subject.keywordAuthortumor microenvironment-
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