grant

Development of integrated risk models of genetic and non-genetic risk factors in endometrial cancer across diverse ancestries

Organization FEINSTEIN INSTITUTE FOR MEDICAL RESEARCHLocation MANHASSET, UNITED STATESPosted 2 Sept 2024Deadline 31 Aug 2026
NIHUS FederalResearch GrantFY2024AddressAdult-Onset Diabetes MellitusAll of Us ProgramAll of Us Research ProgramAll of Us Research ProjectAllelesAllelomorphsAoURPAssessment instrumentAssessment toolAutomobile DrivingBMIBMI percentileBMI z-scoreBody mass indexCOCA1CancersCandidate Disease GeneCandidate GeneCatalogsCausalityCodeCoding SystemComplexCowden SyndromeCowden's DiseaseCox Proportional Hazards ModelsDNA Mismatch Repair Gene HomologueDataData SetDeath RateDetectionDevelopmentDiabetes MellitusDiagnosisDiagnostic MethodDiagnostic ProcedureDiagnostic TechniqueDiseaseDisorderDisparitiesDisparityEarly DiagnosisEndometrialEndometrial CancerEndometrial CarcinomaEndometrium CancerEndometrium CarcinomaEnvironmentEnvironmental FactorEnvironmental Risk FactorEpidemiologyEstrogensEthnic GroupEthnic OriginEthnic PeopleEthnic PopulationEthnic individualEthnicityEthnicity PeopleEthnicity PopulationEtiologyFCC1Familial Nonpolyposis Colon CancerGene InactivationGene SilencingGenesGeneticGenetic AlterationGenetic ChangeGenetic DiversityGenetic ModelsGenetic PredispositionGenetic Predisposition to DiseaseGenetic ScreeningGenetic SusceptibilityGenetic VariationGenetic defectGenetic propensityGerm LinesGoalsHNPCCHNPCC4H_DJ0042M02.9HereditaryHereditary Colo-rectal Endometrial Cancer SyndromeHereditary Colorectal Endometrial Cancer SyndromeHereditary Defective Mismatch Repair SyndromeHereditary Non-Polyposis Colon CancerHereditary Nonpolyposis Colo-rectal CancerHereditary Nonpolyposis Colo-rectal NeoplasmsHereditary Nonpolyposis Colon CancerHereditary Nonpolyposis Colorectal CancerHereditary Nonpolyposis Colorectal NeoplasmsHistologicHistologicallyHistoryIncidenceIndividualInheritedInherited PredispositionInherited SusceptibilityInterventionIntervention StrategiesKetosis-Resistant Diabetes MellitusKnowledgeLS/HNPCCLinkLynch SyndromeMLH1MLH1 geneMMAC1MMAC1 proteinMSH2MSH2 geneMalignant NeoplasmsMalignant TumorMaturity-Onset Diabetes MellitusMetastatic breast cancerMismatch RepairModelingMolecularMultiple Hamartoma SyndromeMutL E Coli Homolog 1MutL E. Coli Homolog 1Mutated in Multiple Advanced Cancers 1MutationNIDDMNon-Insulin Dependent DiabetesNon-Insulin-Dependent Diabetes MellitusNoninsulin Dependent DiabetesNoninsulin Dependent Diabetes MellitusObesityOncogenesisOutcomePHTS genePHTS proteinPMS2PMS2 genePMSL2PTENPTEN genePTEN proteinPTEN1PathogenicityPathway interactionsPatient outcomePatient-Centered OutcomesPatient-Focused OutcomesPatientsPenetrancePerformancePhosphatase and Tensin HomologPhosphatase and Tensin Homolog Deleted on Chromosome 10Polycystic Ovarian DiseasePolycystic Ovarian SyndromePolycystic Ovary SyndromePopulationPopulation HeterogeneityPost-Replication Mismatch RepairPredispositionPreventative strategyPrevention strategyPreventive strategyProteinsPublic HealthPublishingQuetelet indexRaceRacesRacial GroupRecording of previous eventsResearchRiskRisk AssessmentRisk FactorsSamplingSclerocystic Ovarian DegenerationSclerocystic Ovary SyndromeScreening for Endometrial CancerSlow-Onset Diabetes MellitusSocial EnvironmentStable Diabetes MellitusSurvival RateSusceptibilitySymptomsSyndromeT2 DMT2DT2DMTestingTherapeutic EstrogenTimeTrainingType 2 Diabetes MellitusType 2 diabetesType II Diabetes MellitusType II diabetesUnderrepresented GroupsUnderrepresented PopulationsValidationVariantVariationadiposityadult onset diabetesadvanced diseaseadvanced illnessautosomebiobankbiorepositoryblack femaleblack womencancer disparitycancer health disparitycancer invasivenesscancer predispositioncancer riskcancer sub-typescancer subtypescancer-related health disparitycase controlcase-controlledcatalogcausationcohortcomputer based predictioncorpulencecostdetection methoddetection proceduredetection techniquedevelopmentaldiabetesdisease causationdisparities in racedisparity due to racedisparity in cancerdisparity in ethnicdiverse populationsdrivingearly detectionendometrial cancer early detectionentire genomeenvironmental riskepidemiologicepidemiologicalethnic based disparityethnic disadvantageethnic disparityethnic diversityethnic inequalityethnic inequityethnic subgroupethnically diverseethnicity disparityethnicity groupfull genomegenetic etiologygenetic informationgenetic mechanism of diseasegenetic vulnerabilitygenetically predisposedgenome mutationgenome sequencinghereditary non-polyposis colo-rectal cancerhereditary non-polyposis colorectal cancerheterogeneous populationhigh riskhistorieshomologous recombination deficiencyhomologous recombination repair deficiencyimprovedimproved outcomeindexinginequality due to raceinequity due to raceinnovateinnovationinnovativeinsightinterventional strategyketosis resistant diabeteslife-style factorlife-time risklifestyle factorslifetime riskmalignancymaturity onset diabetesmolecular biomarkermolecular markermortalitymortality ratemortality ratiomutated in multiple advanced cancers 1 proteinneoplasm/cancernon-geneticnongeneticnovelpathwaypatient oriented outcomesphosphatase and tensin homologue on chromosome tenpolycystic ovarypolycystic ovary diseasepolycystic ovary disorderpolygenic risk scorepopulation diversitypredictive modelingrace based disparityrace based inequalityrace based inequityrace disparityrace related disparityrace related inequalityrace related inequityracialracial backgroundracial disparityracial diversityracial inequalityracial inequityracial originracial populationracial subgroupracially diverseracially unequalrare allelerare mutationrare variantrisk prediction algorithmrisk prediction modelrisk stratificationscreeningscreeningssocialsocial climatesocial contextsocial culturesocial factorssocio-culturalsocioculturalsocioenvironmentsocioenvironmentalstratify risktranscriptional silencingtumorigenesistype 2 DMtype II DMtype two diabetesunder representation of groupsunder represented groupsunder represented peopleunder represented populationsunderrepresentation of groupsunderrepresented peoplevalidationswhole genome
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Full Description

PROJECT SUMMARY
The incidence of Endometrial Cancer (EC) has been rising, with a notable increase in mortality rates, especially

among Black women who face a higher risk of aggressive EC subtypes. Current diagnostic methods for EC are

invasive, costly, and typically utilized in advanced stages of the disease, highlighting a critical need for early

detection techniques. This project aims to enhance early EC detection and understand the complex interplay of

genetic, social, and environmental factors contributing to EC risk, with a focus on addressing disparities in EC

outcomes among different racial and ethnic groups. In the proposed research, we aim to determine the burden

of rare germline pathogenic variation associated with endometrial cancer risk in racially and ethnically diverse

case control cohorts utilizing the All of USs biobank datasets. This approach will provide new insights into the

genetic factors influencing EC, especially in underrepresented populations. We will create advanced risk models

that integrate a wide array of risk factors, including genetic predispositions and lifestyle factors, into

comprehensive predictive models, combining genetic data with non-genetic factors (e.g., BMI, diabetes history,

PCOS) and validated across different racial and ethnic subgroups, offering a personalized risk assessment tool

for EC. The successful completion of this project will yield a comprehensive understanding of the genetic and

non-genetic factors contributing to EC risk, particularly in racial and ethnic groups that have been historically

understudied. The development of integrated risk models will facilitate early detection of EC, leading to timely

interventions and potentially better survival rates. This project has the potential to revolutionize EC screening

and prevention strategies, making them more effective and accessible across diverse populations, thereby

addressing a significant public health concern.

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Grant Number: 1R21CA294233-01
NIH Institute/Center: NIH

Principal Investigator: Nyasha Chambwe

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