grant

Targeting the cancer glycocalyx

Organization STANFORD UNIVERSITYLocation STANFORD, UNITED STATESPosted 1 Mar 2019Deadline 31 Mar 2029
NIHUS FederalResearch GrantFY2026Acylneuraminyl hydrolaseAdhesion PlaquesAntibodiesBi-specific antibodiesBifunctional AntibodiesBindingBiologicalBispecific AntibodiesCancer ModelCancer PatientCancerModelCancersCathepsinsCell AdhesionCell BodyCell CoatCell Communication and SignalingCell Culture TechniquesCell Growth in NumberCell MultiplicationCell ProliferationCell SignalingCell SurvivalCell TherapyCell ViabilityCell surfaceCell-Matrix Adherens JunctionsCellsCellular AdhesionCellular ProliferationChimeraChimera organismCirculationClinical Treatment MoabDependenceDevelopmentDiseaseDisease ProgressionDisorderEngineeringEsteroproteasesFamilyFc domainFocal AdhesionsFocal ContactsFundingGlycansGlycocalyxGlycoconjugatesGlycoproteinsHumanHuman EngineeringImmuneImmune Cell SuppressionImmune EvasionImmune SurveillanceImmune mediated therapyImmunesImmunologic SurveillanceImmunologically Directed TherapyImmunosuppressionImmunosuppression EffectImmunosuppressive EffectImmunosurveillanceImmunotherapyIntracellular Communication and SignalingKnowledgeLectinLigandsMalignant CellMalignant NeoplasmsMalignant TumorMediatingMetabolic GlycosylationMiceMice MammalsModalityModelingModern ManMolecular InteractionMonoclonal AntibodiesMucinsMucus GlycoproteinMurineMusMyeloid CellsN-Acetylneuraminic AcidsN-Acylneuraminate GlycohydrolasesNeuraminidaseOligosaccharide SialidasePatient outcomePatient-Centered OutcomesPatient-Focused OutcomesPatternPeptidasesPeptide HydrolasesPharmaceutical AgentPharmaceuticalsPharmacologic SubstancePharmacological SubstancePhase 2 Clinical TrialsPhase II Clinical TrialsPhenotypePolysaccharidesProliferatingProtease GeneProteasesProteinasesProteolytic EnzymesReceptor ProteinSialic AcidsSialidaseSignal TransductionSignal Transduction SystemsSignalingSpecificityStructureT-Cell ActivationT-CellsT-LymphocyteTestingTumor AntigensTumor-Associated AntigenVHHVHH antibodyWorkactivate T cellsantigen bindingantigen boundbi-specific T cell engagerbiologicbiological signal transductionbispecific T cell engagerbsAbcamelid antibodycamelid based antibodycamelid derived antibodycamelid derived fragmentcamelid heavy chain only Abscamelid immunoglobulincamelid single chain antibodycamelid variable heavy chaincancer antigenscancer cellcell based interventioncell culturecell culturescell mediated interventioncell mediated therapiescell-based therapeuticcell-based therapycellular therapeuticcellular therapycheck point receptorscheckpoint receptorschimerasclinical translationclinically translatabledevelopmentalexo alpha sialidaseglycosylationimmune evasiveimmune suppressionimmune suppressive activityimmune suppressive functionimmune therapeutic approachimmune therapeutic interventionsimmune therapeutic regimensimmune therapeutic strategyimmune therapyimmune-based therapiesimmune-based treatmentsimmuno therapyimmunosuppressive activityimmunosuppressive functionimmunosuppressive responseinventionmAbsmalignancymembermonoclonal Absmucinasenanobodiesnanobodyneoplasm/cancernew approachesnew therapeutic approachnew therapeutic interventionnew therapeutic strategiesnew therapy approachesnew treatment approachnew treatment strategynovel approachesnovel strategiesnovel strategynovel therapeutic approachnovel therapeutic interventionnovel therapeutic strategiesnovel therapy approachoverexpressoverexpressionpatient oriented outcomespharmaceuticalphase II protocolphysical propertypre-clinical developmentpreclinical developmentprogramsreceptorresponsesdAbsialic acid binding Ig-like lectinsiglecsingle domain antibodiessugartargeted cancer therapythymus derived lymphocytetumor-specific antigenvariable heavy chain antibody
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PROJECT SUMMARY
Altered cell-surface glycosylation is recognized as a hallmark of cancer. Two frequently observed cancer-

associated glyco-phenotypes are hypersialylation and mucin overexpression. These cancer glycosylation

patterns strongly correlate with disease aggressiveness and poor patient outcomes, but until recently their

functional…

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Targeting the cancer glycocalyx — STANFORD UNIVERSITY | UNITED STATES | Mar 2019 | Dev Procure