grant

Elucidating the role of gut microbiota in colitis-associated colorectal cancer

Organization BAYLOR COLLEGE OF MEDICINELocation HOUSTON, UNITED STATESPosted 1 Jan 2023Deadline 31 Dec 2027
NIHUS FederalResearch GrantFY2025AffectAnimal ModelAnimal Models and Related StudiesApoptosisApoptosis PathwayBacteriaBacterial GenesBioinformaticsBiologic ModelsBiologicalBiological ModelsBiopsyBowel CancerCancer DetectionCancer InductionCancer TreatmentCancersChronicClinicalClinical ResearchClinical StudyColitis associated colon cancerColitis associated colorectal cancerColitis induced colorectal cancerColonColorectal CancerDNA DamageDNA InjuryDSS colitisDSS modelDSS mouse modelDSS-induced acute colitisDSS-induced colitisDevelopmentDiseaseDisorderEnzyme GeneEnzymesEpitheliumEventGI microbiomeGI microbiotaGastrointestinal microbiotaGeneral TaxonomyGenesGenome InstabilityGenomic InstabilityGut MucosaHost FactorHost Factor ProteinHumanImmune responseIn VitroIndividualInflammationInflammatoryInflammatory Bowel DiseasesInflammatory Bowel DisorderIntegration Host FactorsIntermediary MetabolismIntestinal CancerInvestigationKnowledgeLaboratoriesLightLongitudinal StudiesMalignant Intestinal NeoplasmMalignant Intestinal TumorMalignant Neoplasm TherapyMalignant Neoplasm TreatmentMalignant NeoplasmsMalignant TumorMetabolic ProcessesMetabolismMiceMice MammalsModel SystemModelingModern ManMolecularMucosaMucosal TissueMucous MembraneMurineMusOrganoidsOxidative StressPathogenesisPathway interactionsPatientsPhotoradiationProgrammed Cell DeathProliferatingProteomeProteomicsRectumResearchResearch ResourcesResearch SpecimenResourcesRiskRoleSamplingSignal PathwaySpecimenStructureStudy modelsSurfaceSystemSystems BiologyTaxonomyTechniquesTechnologyUlcerated ColitisUlcerative ColitisWorkanti-cancer therapybiologiccancer preventioncancer progressioncancer riskcancer therapycancer-directed therapycarcinogenesiscolitis associated cancercolitis induced colon cancercolitis-induced dysbiosiscommunity microbesdesigndesigningdevelopmentaldextran sulfate sodium colitisdextran sulfate sodium induced colitisdextran sulfate sodium modeldextran sulfate sodium mouse modeldigestive tract microbiomedysbacteriosisdysbiosisdysbioticenteric microbial communityenteric microbiomeenteric microbiotafecal microbial communityfecal microbiotagastrointestinal microbial floragastrointestinal microbiomegut communitygut floragut microbe communitygut microbesgut microbial communitygut microbial compositiongut microbial consortiagut microbial speciesgut microbiomegut microbiotagut microbioticgut microfloragut-associated microbiomehost responsehuman florahuman microbial communitieshuman microbiotahuman microflorahuman-associated microbial communitieshuman-associated microbiotaimmune system responseimmunoresponsein vivoinflammatory disease of the intestineinflammatory disorder of the intestineinnovateinnovationinnovativeinterestintestinal autoinflammationintestinal biomeintestinal floraintestinal microbesintestinal microbiomeintestinal microbiotaintestinal microfloraintestinal tract microfloraintestine cancerlong-term studylongitudinal outcome studiesmalignancymalignant intestine neoplasmmalignant intestine tumormetaproteomicsmicrobe communitymicrobialmicrobial communitymicrobial consortiamicrobial floramicrobial imbalancemicrobiomemicrobiome community compositionmicrobiome compositionmicrobiome species compositionmicrobiome structuremicrobiotamicrobiota compositionmicrobiota patternsmicrobiota profilesmicrobiota signaturemicrofloramicroorganism communitymodel of animalmouse modelmucosa-associated microbesmucosa-associated microbial communitymucosa-associated microbiotamucosal floramucosal microbesmucosal microbiotamucosal microfloramultispecies consortiamurine modelneoplasm progressionneoplasm/cancerneoplastic progressionnew approachesnew diagnosticsnew technologynew therapeutic approachnew therapeutic interventionnew therapeutic strategiesnew therapy approachesnew treatment approachnew treatment strategynext generation diagnosticsnovel approachesnovel diagnosticsnovel strategiesnovel strategynovel technologiesnovel therapeutic approachnovel therapeutic interventionnovel therapeutic strategiesnovel therapy approachpathwayphospho-proteomicsphosphoproteomicspolymicrobial communityprotein expressionresponsesocial rolestatisticstooltranslational opportunitiestranslational potentialtumor progressiontumorigenic
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Full Description

Abstract
Patients with ulcerative colitis (UC), an inflammatory bowel disease (IBD), have an increased risk of developing

colitis-associated colorectal cancer (CAC). Human gut microbiome composition has recently been associated

with a wide array of diseases, including IBD and colorectal cancer. Studies have shown that gut microbiota

could influence colon epithelium to initiate or promote colorectal cancer development directly or indirectly.

However, little is known on the structure and function of the microbiota in CAC and how they implicate the

development of CAC at the molecular level. In this study, we will investigate the role of microbiota in the

development of CAC, as well as the molecular events underlying the interplay of microbiota and host response.

The project builds upon our previous studies in examining the genomic instabilities and proteome alterations in

the colon epithelium during the pathogenesis of IBD-CAC, and will focus on the mechanistic and functional

involvement of the microbiome and their components in the modulation (by protective bacteria) or activation

(by tumorigenic bacteria) of CAC development. Specifically, we will investigate the implication of mucosa-

associated microbiota in CAC by an integrated approach using three model systems, including clinical

specimens (Aim 1), in vitro microbial cultivation and organoid models (Aim 2), and in vivo mouse model (Aim

3). Our integrative, state-of-the-art approach will characterize the composition, functional genes and pathways

of the microbiome implicated in CAC, and the impact of microbiota on colon mucosa. By studying the gut

microbiota and its interplay with the colon host using novel approaches and cutting-edge technology, our study

has significant translational potential that could lead to establishing the gut microbiome as predictors of CAC

risk and aid in developing approaches for CAC prevention and detection in IBD patients.

Grant Number: 5R01CA276173-03
NIH Institute/Center: NIH

Principal Investigator: Ru Chen

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