Full metadata record

DC Field Value Language
dc.contributor.authorPark, Jinyoung-
dc.contributor.authorCho, Jinhong-
dc.contributor.authorSong, Eun Joo-
dc.date.accessioned2024-01-19T16:04:39Z-
dc.date.available2024-01-19T16:04:39Z-
dc.date.created2021-09-02-
dc.date.issued2020-11-
dc.identifier.issn0253-6269-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/117904-
dc.description.abstractThe ubiquitin-proteasome system (UPS) plays an important role in the cellular processes for protein quality control and homeostasis. Dysregulation of the UPS has been implicated in numerous diseases, including cancer. Indeed, components of UPS are frequently mutated or abnormally expressed in various cancers. Since Bortezomib, a proteasome inhibitor, received FDA approval for the treatment of multiple myeloma and mantle cell lymphoma, increasing numbers of researchers have been seeking drugs targeting the UPS as a cancer therapeutic strategy. Here, we introduce the essential component of UPS, including ubiquitinating enzymes, deubiquitinating enzymes and 26S proteasome, and we summarize their targets and mechanisms that are crucial for tumorigenesis. In addition, we briefly discuss some UPS inhibitors, which are currently in clinical trials as cancer therapeutics.-
dc.languageEnglish-
dc.publisherPHARMACEUTICAL SOC KOREA-
dc.subjectMULTIPLE-MYELOMA CELLS-
dc.subjectCANCER THERAPEUTIC TARGET-
dc.subjectSMALL-MOLECULE INHIBITOR-
dc.subjectTUMOR-SUPPRESSOR CYLD-
dc.subjectFATTY-ACID SYNTHASE-
dc.subjectNF-KAPPA-B-
dc.subjectBREAST-CANCER-
dc.subjectIN-VIVO-
dc.subjectPROMOTES PROLIFERATION-
dc.subjectCYCLIN-E-
dc.titleUbiquitin-proteasome system (UPS) as a target for anticancer treatment-
dc.typeArticle-
dc.identifier.doi10.1007/s12272-020-01281-8-
dc.description.journalClass1-
dc.identifier.bibliographicCitationARCHIVES OF PHARMACAL RESEARCH, v.43, no.11, pp.1144 - 1161-
dc.citation.titleARCHIVES OF PHARMACAL RESEARCH-
dc.citation.volume43-
dc.citation.number11-
dc.citation.startPage1144-
dc.citation.endPage1161-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.identifier.kciidART002654749-
dc.identifier.wosid000588005000001-
dc.identifier.scopusid2-s2.0-85095605596-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeReview-
dc.subject.keywordPlusMULTIPLE-MYELOMA CELLS-
dc.subject.keywordPlusCANCER THERAPEUTIC TARGET-
dc.subject.keywordPlusSMALL-MOLECULE INHIBITOR-
dc.subject.keywordPlusTUMOR-SUPPRESSOR CYLD-
dc.subject.keywordPlusFATTY-ACID SYNTHASE-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusBREAST-CANCER-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusPROMOTES PROLIFERATION-
dc.subject.keywordPlusCYCLIN-E-
dc.subject.keywordAuthorUbiquitin&#8211-
dc.subject.keywordAuthorproteasome system (UPS)-
dc.subject.keywordAuthorE3 ligase-
dc.subject.keywordAuthorDeubiquitinating enzymes (DUBs)-
dc.subject.keywordAuthorProteasome-
dc.subject.keywordAuthorCancer-
dc.subject.keywordAuthorSmall molecule inhibitors-
Appears in Collections:
KIST Article > 2020
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE