grant

Northwestern University Center for Chromatin NanoImaging in Cancer (NU-CCNIC)

Organization NORTHWESTERN UNIVERSITYLocation Chicago, UNITED STATESPosted 10 Dec 2021Deadline 30 Nov 2026
NIHUS FederalResearch GrantFY20253-D3-D structure3-Dimensional3-dimensional structure3D3D structureActive Follow-upAddressAfter CareAfter-TreatmentAftercareAssayBioassayBiological AssayCancer BiologyCancersCell BodyCell FunctionCell NucleusCell PhysiologyCell ProcessCellsCellular FunctionCellular PhysiologyCellular ProcessChromatinChromatin StructureComplexComputing MethodologiesCytotoxic ChemotherapyCytotoxic TherapyDNADataData SetDeoxyribonucleic AcidDevelopmentDiameterDisease remissionDisparateElectron MicroscopyEpigeneticEpigenetic ChangeEpigenetic MechanismEpigenetic ProcessEventFeedbackFosteringFutureGene TranscriptionGeneralized GrowthGenesGeneticGenetic TranscriptionGenome MappingsGenomicsGrowthHeterogeneityImageImaging ProceduresImaging TechnicsImaging TechniquesImaging technologyKnowledgeLabelLengthLinkMalignant CellMalignant NeoplasmsMalignant TumorMethodsMicroscopyMissionMolecularMolecular ConfigurationMolecular ConformationMolecular Modeling Nucleic Acid BiochemistryMolecular Modeling Protein/Amino Acid BiochemistryMolecular ModelsMolecular StereochemistryMolecular TargetNanoscopyNucleusOncologyOncology CancerOpticsPathway interactionsPatternPhysicsPlayPopulationProcessRNA ExpressionRelapseRemissionResearchResistanceResistance developmentResistant developmentResolutionRoleScanningSeriesSightSolidStem Cell ResearchSubcellular ProcessTechniquesTechnologyTestingTherapeuticTimeTissue GrowthTranscriptionTranslatingTransmission Electron MicroscopyUniversitiesVisionVisualizationactive followupanti-cancer researchanti-cancer therapeuticcancer cellcancer progenitorcancer progenitor cellscancer progressioncancer researchcancer stem cellcancer stem like cellcell imagingcellular imagingchemotherapycomputational methodologycomputational methodscomputer based methodcomputer methodscomputing methodconformationconformationalconformational stateconformationallyconformationsdata modelingdeveloping resistancedevelopmentalelectron tomographyepigeneticallyepigenomicsfollow upfollow-upfollowed upfollowupfrontierimagingimaging capabilitiesimaging platforminsightlive cell microscopymalignancymalignant progenitormalignant stem cellmodel of datamodel the datamodeling of the datamolecular imagingmolecular modelingmolecular scalemolecule imagingnano meter scalenano meter sizednano-sized sensorsnanoimagingnanometer scalenanometer sizednanoscalenanosensingnanosensorsneoplasm progressionneoplasm/cancerneoplastic progressionnew drug treatmentsnew drugsnew pharmacological therapeuticnew technologynew therapeutic approachnew therapeutic interventionnew therapeutic strategiesnew therapeuticsnew therapynew therapy approachesnew treatment approachnew treatment strategynext generation therapeuticsnovel drug treatmentsnovel drugsnovel pharmaco-therapeuticnovel pharmacological therapeuticnovel technologiesnovel therapeutic approachnovel therapeutic interventionnovel therapeutic strategiesnovel therapeuticsnovel therapynovel therapy approachoncogenic progenitoroncogenic stem cellsontogenyopticalpathwaypost treatmentpressurepreventpreventingprogenitor biologyprogenitor cell biologyprogenitor like cancer cellprogramsquantitative imagingresistance to therapyresistantresistant to therapyresolutionssingle cell genomicssingle moleculesocial rolespatial and temporalspatial temporalspatiotemporalstemstem and progenitor biologystem cell biologystem cell studystem like cancer cellstressorsuper high resolutionsuperresolutiontech developmenttechnology developmenttemporal measurementtemporal resolutiontherapeutic resistancetherapeutically effectivetherapy resistantthree dimensionalthree dimensional structuretime measurementtranscriptional reprogrammingtreatment resistancetumortumor progressionultra high resolutionvisual function
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Full Description

Overall: PROJECT SUMMARY
Cancer stem cells (CSCs) play a critical role in fostering tumor resistance to therapies and relapse after

treatment. This presents a crucial barrier to the development of successful anti-cancer therapeutics.

Transcriptional reprogramming and plasticity play a critical role in and out of the CSC state, which in turn are

interdependent on the regulatory function of the three-dimensional (3D) structure of chromatin, epigenetic states,

and other molecular events. Our understanding of fundamental CSC biology has been hampered by the need

for cellular nanoscale imaging technologies that provide both highly detailed structural information regarding 3D

chromatin organization and highly multiplexed molecular imaging of the many molecular regulators and events

involved in CSC processes. We propose to establish the Northwestern University Center for Chromatin

Nanoimaging in Cancer (NU-CCNIC) to address this fundamental technology gap in cellular nanoscale imaging

and deploy the new technologies to address the fundamental knowledge gap in CSC biology. The Center

converges experts in cellular nanoscale imaging, computational imaging, molecular modeling, computational

genomics, CSC biology, and oncology. The Center will develop, test, validate, iterate, and deploy an integrated

and co-registered Multi-scale Chromatin Nanoimaging Platform that will comprise three “nested-doll” imaging

techniques: chromatin scanning transmission electron microscopy, optical spectroscopic super-resolution

nanoscopy, and optical spectroscopic nanosensing. The Nanoimaging Platform will enable quantitative imaging

of chromatin structure and highly multiplexed molecular and gene-specific localization, at the most fundamental

length-scale approaching 1 nm resolution, including the imaging of statistically significant cell populations and

live cells with high temporal resolution over prolonged temporal follow-up times. The Nanoimaging Platform will

be bridged to computational genomics, epigenomics, genome mapping, and predictive transcriptional modeling

datasets. These technologies will be deployed to answer several long-standing open questions in CSC biology.

We will elucidate whether CSCs can originate from non-CSCs via transcriptional reprogramming, test the role of

chromatin structure in fostering transcriptional plasticity in CSC processes, and explore the possibility of

transcriptionally reprogramming CSCs to exit the stem-state as a new therapeutic strategy. All aspects of the

technology development will be guided by the needs of the CSC biology testbed through a series of research

feedback loops. In the long term, such single-cell nanoimaging technologies will help comprehensive

understanding of the complex interplay between structural, physico-chemical, and molecular genomic events.

We anticipate that these convergence studies will provide new insights into CSC biology, which are impossible

to reveal with the use of any single method, and open new opportunities for identifying therapeutic strategies.

Grant Number: 5U54CA268084-04
NIH Institute/Center: NIH

Principal Investigator: Vadim Backman

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