grant

PROSPECT-Global Consortium and Risk Factor Discovery

Organization WASHINGTON UNIVERSITYLocation SAINT LOUIS, UNITED STATESPosted 1 May 2024Deadline 30 Apr 2027
NIHUS FederalResearch GrantFY2024AddressAdenomatous PolypsAgeAlcohol Chemical ClassAlcoholsAnimal ModelAnimal Models and Related StudiesAutoregulationBiochemicalBiologic FactorBiologic ModelsBiologicalBiological FactorsBiological ModelsBirthBloodBlood Reticuloendothelial SystemBody TissuesCRC preventionCancersCausalityCell BodyCellsCharacteristicsChemicalsCollaborationsColonColorectal CancerComputational BiologyDNA MethylationDataDevelopmentDietDimensionsDisciplineEcologic SystemsEcological SystemsEcosystemElectronic Health RecordEnvironmentEnvironmental FactorEnvironmental Risk FactorEpidemiologic DeterminantsEpidemiologic FactorsEpidemiological FactorsEpidemiologyEpigeneticEpigenetic ChangeEpigenetic MechanismEpigenetic ProcessEthnic OriginEthnicityEtiologyExposure toFecesFunctional MetagenomicsFutureGI microbiomeGene TranscriptionGenerationsGenetic TranscriptionGenomicsGeographyGoalsHomeostasisImmunologyIncidenceIndividualInterventionIntervention StrategiesInvestigationLesionLife CycleLife Cycle StagesLife StyleLifestyleLinkLocationMalignant NeoplasmsMalignant TumorMediatingMetagenomicsMindModel SystemModelingModificationMolecularOncogenesisParturitionPhasePhysiologicPhysiologicalPhysiological HomeostasisPopulationPositionPositioning AttributePredispositionPreventative strategyPreventionPrevention strategyPreventive strategyProcessProspective StudiesQuestionnairesRNA ExpressionRaceRacesResearchResearch ActivityResolutionRiskRisk AssessmentRisk FactorsRoleSightSusceptibilityTechnologyTissuesTranscriptionTranslatingTransmissionUniversitiesVisionWashingtonWorkadenomaagesanti-cancer researchbiologicbiological specimen archivesbiosample archivebiospecimen archivecancer initiationcancer progressioncancer researchcausationcohortcolorectal cancer preventioncolorectal cancer riskcomputer biologydata harmonizationdevelopmentaldietsdigestive tract microbiomedisease causationearly colo-rectal cancerearly colorectal cancerearly onsetearly onset colo-rectal adenomaearly onset colo-rectal cancerearly onset colorectal adenomaearly onset colorectal cancerelectronic health care recordelectronic health medical recordelectronic health plan recordelectronic health registryelectronic medical health recordenteric microbiomeenvironmental riskepidemiologicepidemiologicalepigeneticallyepigenomegastrointestinal microbiomegut microbiomegut-associated microbiomeharmonized datahigh riskhuman dataimprintindividualized preventioninnovateinnovationinnovativeinterventional strategyintestinal biomeintestinal microbiomelife courselife spanlife style interventionlifespanlifestyle interventionmalignancymicrobial signaturemicrobiomemodel of animalneoplasm progressionneoplasm/cancerneoplastic progressionnovelobesigenicobesogenicpersonalized preventionpharmacologicpolypoid adenomaprecision preventionprevent colorectal cancerprogenitor biologyprogenitor cell biologyracialracial backgroundracial originresolutionsresponsesmall moleculesocialsocial determinantssocial rolesociodeterminantspecimen archivestem and progenitor biologystem cell biologystooltransmission processtumor initiationtumor progressiontumorigenesisvisual functionyoung colo-rectal canceryoung colorectal canceryoung onset colo-rectal canceryoung onset colorectal cancer
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Full Description

ABSTRACT
Our vision is to unravel and ultimately reverse the intricate network of causal factors throughout the life course

that disrupts biological homeostasis to promote colorectal cancer (CRC) among individuals younger than age 50

years. Uniting leading scientific minds in early-onset colorectal cancer (EOCRC) research and complementary

fields, we have embraced disruptive, transdisciplinary approaches spanning cells to individuals to populations to

address the core Grand Challenge to “Determine why the incidence of early-onset cancers is rising globally”. We

will address specific questions of “the mechanisms linking lifetime exposures with cancer initiation and

promotion” by focusing on EOCRC as an ideal model for early-onset cancer due to the availability of well-

characterized animal models and well-established and prevalent precursor lesion, the adenomatous polyp

(adenoma), offering a unique opportunity for interception and prevention. Our work will transform the field by

directly addressing our overarching goal to “identify and understand the processes through which different

biological and environmental factors cause early-onset cancers”, and reverse the burden in a timely, effective,

feasible, inclusive fashion. Our team, both working independently and in collaboration, has uncovered several

risk factors that are likely to be drivers for the rising incidence for EOCRC. We are now uniquely positioned to

translate etiologic understanding to actionable prevention by identifying novel factors, including environmental

and social determinants, and deepening our understanding into overlooked dimensions of exposure throughout

the life course. The unprecedented scope and scale of our proposal can only be supported through Cancer

Grand Challenges since our “high-risk” disruptive approach requires deep interactions between work packages

(WP)s led by leaders in diverse disciplines. This will enable incorporation of fresh perspectives to move beyond

traditional risk-factor epidemiology toward an integrated, mechanistically-informed model with population scale

and cellular resolution of the multiple and cumulative “hits” that promote EOCRC to inform the development of

actionable prevention. Our innovations intersect epidemiology, small molecule discovery, genomics, stem cell

biology, immunology, and computational biology with these key features: 1) harmonization of diverse cohorts

with data and biospecimens collected across the lifecourse; 2) innovative and reliable analysis of small molecules

to detect novel exposures; 3) high-resolution technologies for analysis of target tissues; 4) model systems

capable of interrogating accumulating exposures across the lifespan and their impact on the cellular ecosystem;

5) prevention through risk assessment and pharmacologic/lifestyle interventions. Collectively, our work will serve

as an exemplar for transforming research into other early-onset cancers.

Grant Number: 1OT2CA297576-01
NIH Institute/Center: NIH

Principal Investigator: Yin Cao

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