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dc.contributor.authorZayed, A.en
dc.contributor.authorAl-Saedi, D. A.en
dc.contributor.authorMensah, E. O.en
dc.contributor.authorKanwugu, O. N.en
dc.contributor.authorAdadi, P.en
dc.contributor.authorUlber, R.en
dc.date.accessioned2025-02-25T11:02:22Z-
dc.date.available2025-02-25T11:02:22Z-
dc.date.issued2024-
dc.identifier.citationZayed, A., Al-Saedi, D. A., Mensah, E., Kanwugu, O., Adadi, P., & Ulber, R. (2024). Fucoidan’s Molecular Targets: A Comprehensive Review of Its Unique and Multiple Targets Accounting for Promising Bioactivities Supported by In Silico Studies. Marine Drugs, 22(1), [29]. https://doi.org/10.3390/md22010029apa_pure
dc.identifier.issn1660-3397-
dc.identifier.otherFinal2
dc.identifier.otherAll Open Access; Gold Open Access; Green Open Access3
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85183085868&doi=10.3390%2fmd22010029&partnerID=40&md5=e0ed6888a86841ac878e1e4b4d40615c1
dc.identifier.otherhttps://www.mdpi.com/1660-3397/22/1/29/pdf?version=1703923666pdf
dc.identifier.urihttp://elar.urfu.ru/handle/10995/141720-
dc.description.abstractFucoidan is a class of multifunctional polysaccharides derived from marine organisms. Its unique and diversified physicochemical and chemical properties have qualified them for potential and promising pharmacological uses in human diseases, including inflammation, tumors, immunity disorders, kidney diseases, and diabetes. Physicochemical and chemical properties are the main contributors to these bioactivities. The previous literature has attributed such activities to its ability to target key enzymes and receptors involved in potential disease pathways, either directly or indirectly, where the anionic sulfate ester groups are mainly involved in these interactions. These findings also confirm the advantageous pharmacological uses of sulfated versus non-sulfated polysaccharides. The current review shall highlight the molecular targets of fucoidans, especially enzymes, and the subsequent responses via either the upregulation or downregulation of mediators’ expression in various tissue abnormalities. In addition, in silico studies will be applied to support the previous findings and show the significant contributors. The current review may help in understanding the molecular mechanisms of fucoidan. Also, the findings of this review may be utilized in the design of specific oligomers inspired by fucoidan with the purpose of treating life-threatening human diseases effectively. © 2023 by the authors.en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.rightscc-byother
dc.sourceMarine Drugs2
dc.sourceMarine Drugsen
dc.subjectBIOACTIVITIESen
dc.subjectFUCOIDANen
dc.subjectINFLAMMATION MARKERSen
dc.subjectMOLECULAR MECHANISMSen
dc.subjectSIGNALING PATHWAYSen
dc.subjectDOWN-REGULATIONen
dc.subjectESTERSen
dc.subjectHUMANSen
dc.subjectINFLAMMATIONen
dc.subjectPOLYSACCHARIDESen
dc.subjectSULFATESen
dc.subject2 (2 AMINO 3 METHOXYPHENYL)CHROMONEen
dc.subjectADEZMAPIMODen
dc.subjectALPHA INTERFERONen
dc.subjectALPHA SMOOTH MUSCLE ACTINen
dc.subjectCATALASEen
dc.subjectCONNECTIVE TISSUE GROWTH FACTORen
dc.subjectCYCLIN D1en
dc.subjectCYCLIN DEPENDENT KINASE 4en
dc.subjectCYCLIN DEPENDENT KINASE 6en
dc.subjectCYCLIN Een
dc.subjectCYCLOOXYGENASE 1en
dc.subjectCYCLOOXYGENASE 2en
dc.subjectEPIDERMAL GROWTH FACTORen
dc.subjectEPIDERMAL GROWTH FACTOR RECEPTORen
dc.subjectFUCOIDINen
dc.subjectG PROTEIN COUPLED RECEPTORen
dc.subjectGAMMA INTERFERONen
dc.subjectGLUCOSE TRANSPORTER 4en
dc.subjectGLUTATHIONE PEROXIDASEen
dc.subjectGLYCOGEN SYNTHASE KINASE 3BETAen
dc.subjectHEME OXYGENASE 1en
dc.subjectIMMUNOGLOBULIN ENHANCER BINDING PROTEINen
dc.subjectINDOMETACINen
dc.subjectINDUCIBLE NITRIC OXIDE SYNTHASEen
dc.subjectINTERLEUKIN 12en
dc.subjectINTERLEUKIN 1BETAen
dc.subjectINTERLEUKIN 6en
dc.subjectKELCH LIKE ECH ASSOCIATED PROTEIN 1en
dc.subjectLAPATINIBen
dc.subjectMACROPHAGE DERIVED CHEMOKINEen
dc.subjectMALONALDEHYDEen
dc.subjectMITOGEN ACTIVATED PROTEIN KINASEen
dc.subjectMITOGEN ACTIVATED PROTEIN KINASE 1en
dc.subjectMITOGEN ACTIVATED PROTEIN KINASE 3en
dc.subjectMYELOID DIFFERENTIATION FACTOR 88en
dc.subjectNEUROPILIN 1en
dc.subjectNEUROPILIN 2en
dc.subjectOLIGOMERen
dc.subjectPATHOGEN ASSOCIATED MOLECULAR PATTERNen
dc.subjectPEROXISOME PROLIFERATOR ACTIVATED RECEPTOR GAMMAen
dc.subjectPHOSPHATIDYLINOSITOL 3 KINASEen
dc.subjectPLATELET DERIVED GROWTH FACTORen
dc.subjectPOLYSACCHARIDEen
dc.subjectPROTEIN BAXen
dc.subjectPROTEIN BCL 2en
dc.subjectPROTEIN KINASE Ben
dc.subjectRAB PROTEINen
dc.subjectRAS PROTEINen
dc.subjectREACTIVE OXYGEN METABOLITEen
dc.subjectSMAD2 PROTEINen
dc.subjectSMAD3 PROTEINen
dc.subjectSMAD4 PROTEINen
dc.subjectSUPEROXIDE DISMUTASEen
dc.subjectTOLL LIKE RECEPTOR 2en
dc.subjectTOLL LIKE RECEPTOR 4en
dc.subjectTRANSCRIPTION FACTOR NRF2en
dc.subjectTRANSCRIPTION FACTOR RELAen
dc.subjectTUMOR NECROSIS FACTORen
dc.subjectVASCULOTROPINen
dc.subjectESTERen
dc.subjectFUCOIDINen
dc.subjectPOLYSACCHARIDEen
dc.subjectSULFATEen
dc.subject3T3-L1 CELL LINEen
dc.subjectA-549 CELL LINEen
dc.subjectALZHEIMER DISEASEen
dc.subjectANGIOGENESISen
dc.subjectANTIINFLAMMATORY ACTIVITYen
dc.subjectAPOPTOSISen
dc.subjectARPE-19 CELL LINEen
dc.subjectAUTOIMMUNE DISEASEen
dc.subjectBINDING AFFINITYen
dc.subjectBIOLOGICAL ACTIVITYen
dc.subjectBREAST CANCERen
dc.subjectCARDIOVASCULAR DISEASEen
dc.subjectCATARACTen
dc.subjectCELL GROWTHen
dc.subjectCELL MIGRATIONen
dc.subjectCELL PROLIFERATIONen
dc.subjectCELL SURVIVALen
dc.subjectCHROMOSOME ABERRATIONen
dc.subjectCOMPUTER MODELen
dc.subjectDIABETES MELLITUSen
dc.subjectDNA BINDINGen
dc.subjectDOWN REGULATIONen
dc.subjectDROSOPHILA MELANOGASTERen
dc.subjectDU145 CELL LINEen
dc.subjectENDOCYTOSISen
dc.subjectEPITHELIAL MESENCHYMAL TRANSITIONen
dc.subjectERYTHROLEUKEMIAen
dc.subjectHEAT SHOCKen
dc.subjectHEMATOPOIESISen
dc.subjectHEP-G2 CELL LINEen
dc.subjectHUVEC CELL LINEen
dc.subjectHYPEROXIA-INDUCED LUNG INJURYen
dc.subjectHYPERTENSIONen
dc.subjectINFLAMMATIONen
dc.subjectIONIZING RADIATIONen
dc.subjectKIDNEY DISEASEen
dc.subjectL-02 CELL LINEen
dc.subjectLIVER CELL CARCINOMAen
dc.subjectLIVER FIBROSISen
dc.subjectLIVER NECROSISen
dc.subjectLUNG CANCERen
dc.subjectMAPK SIGNALINGen
dc.subjectMCF-7 CELL LINEen
dc.subjectMDA-MB-231 CELL LINEen
dc.subjectMELANOMAen
dc.subjectMETABOLIC SYNDROME Xen
dc.subjectMETASTATIC COLORECTAL CANCERen
dc.subjectMICROGLIAen
dc.subjectMOLECULAR DOCKINGen
dc.subjectMTOR SIGNALINGen
dc.subjectNCI-H1650 CELL LINEen
dc.subjectNF KB SIGNALINGen
dc.subjectNK-92 CELL LINEen
dc.subjectNONHUMANen
dc.subjectOSSIFICATIONen
dc.subjectOSTEOPOROSISen
dc.subjectOXIDATIVE STRESSen
dc.subjectPANCREAS CANCERen
dc.subjectPHYSICAL CHEMISTRYen
dc.subjectPI3K/AKT SIGNALINGen
dc.subjectPROTEIN PHOSPHORYLATIONen
dc.subjectRAW 264.7 CELL LINEen
dc.subjectRETINAL PIGMENT EPITHELIUMen
dc.subjectREVIEWen
dc.subjectRHEUMATOID ARTHRITISen
dc.subjectSH-SY5Y CELL LINEen
dc.subjectTGF BETA SIGNALINGen
dc.subjectULTRAVIOLET RADIATIONen
dc.subjectUPREGULATIONen
dc.subjectHUMANen
dc.subjectINFLAMMATIONen
dc.titleFucoidan’s Molecular Targets: A Comprehensive Review of Its Unique and Multiple Targets Accounting for Promising Bioactivities Supported by In Silico Studiesen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.3390/md22010029-
dc.identifier.scopus85183085868-
local.contributor.employeeZayed A., Institute of Bioprocess Engineering, Rheinland-Pfälzische Technische Universität Kaiserslautern-Landau, Gottlieb-Daimler-Straße 49, Kaiserslautern, 67663, Germany, Department of Pharmacognosy, College of Pharmacy, Tanta University, El-Guish Street (Medical Campus), Tanta, 31527, Egypten
local.contributor.employeeAl-Saedi D.A., Department of Biochemistry, Faculty of Sciences, King Abdulaziz University, Jeddah, 21589, Saudi Arabiaen
local.contributor.employeeMensah E.O., Faculty of Ecotechnology, ITMO University, Lomonosova Street 9, Saint Petersburg, 191002, Russian Federationen
local.contributor.employeeKanwugu O.N., Institute of Chemical Engineering, Ural Federal University, Mira Street 28, Yekaterinburg, 620002, Russian Federation, ARC Centre of Excellence in Synthetic Biology, School of Natural Sciences, Macquarie University, Sydney, 2109, NSW, Australiaen
local.contributor.employeeAdadi P., Department of Food Science, University of Otago, Dunedin, 9054, New Zealanden
local.contributor.employeeUlber R., Institute of Bioprocess Engineering, Rheinland-Pfälzische Technische Universität Kaiserslautern-Landau, Gottlieb-Daimler-Straße 49, Kaiserslautern, 67663, Germanyen
local.issue1-
local.volume22-
dc.identifier.wos001151140200001-
local.contributor.departmentInstitute of Bioprocess Engineering, Rheinland-Pfälzische Technische Universität Kaiserslautern-Landau, Gottlieb-Daimler-Straße 49, Kaiserslautern, 67663, Germanyen
local.contributor.departmentDepartment of Pharmacognosy, College of Pharmacy, Tanta University, El-Guish Street (Medical Campus), Tanta, 31527, Egypten
local.contributor.departmentDepartment of Biochemistry, Faculty of Sciences, King Abdulaziz University, Jeddah, 21589, Saudi Arabiaen
local.contributor.departmentFaculty of Ecotechnology, ITMO University, Lomonosova Street 9, Saint Petersburg, 191002, Russian Federationen
local.contributor.departmentInstitute of Chemical Engineering, Ural Federal University, Mira Street 28, Yekaterinburg, 620002, Russian Federationen
local.contributor.departmentARC Centre of Excellence in Synthetic Biology, School of Natural Sciences, Macquarie University, Sydney, 2109, NSW, Australiaen
local.contributor.departmentDepartment of Food Science, University of Otago, Dunedin, 9054, New Zealanden
local.identifier.pure52291891-
local.description.order29
local.identifier.eid2-s2.0-85183085868-
local.identifier.wosWOS:001151140200001-
local.identifier.pmid38248653-
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