grant

Investigating the mechanisms of driver genes associated with ancestry and aggressiveness in prostate cancer

Organization BOSTON UNIVERSITY MEDICAL CAMPUSLocation BOSTON, UNITED STATESPosted 10 May 2021Deadline 30 Apr 2027
NIHUS FederalResearch GrantFY2025AT-binding transcription factor 1ATBF1AffectAfrican AmericanAfrican American groupAfrican American individualAfrican American peopleAfrican American populationAfrican AmericansAfro AmericanAfroamericanAge of OnsetAmericanAmerican maleAmerican manAmerican menBiochemicalBiologicalBostonCRISPR approachCRISPR based approachCRISPR methodCRISPR methodologyCRISPR techniqueCRISPR technologyCRISPR toolsCRISPR-CAS-9CRISPR-based methodCRISPR-based techniqueCRISPR-based technologyCRISPR-based toolCRISPR/CAS approachCRISPR/Cas methodCRISPR/Cas technologyCRISPR/Cas9CRISPR/Cas9 technologyCancer BiologyCancer GenesCancer-Promoting GeneCancersCas nuclease technologyCell BodyCell LineCell modelCellLineCellsCellular ExpansionCellular GrowthCellular modelChemical FractionationClinicalClustered Regularly Interspaced Short Palindromic Repeats approachClustered Regularly Interspaced Short Palindromic Repeats methodClustered Regularly Interspaced Short Palindromic Repeats methodologyClustered Regularly Interspaced Short Palindromic Repeats techniqueClustered Regularly Interspaced Short Palindromic Repeats technologyCollectionCommunitiesComplementComplement ProteinsDNA AlterationDNA Sequence AlterationDNA mutationDataDeath RateDiagnosisDimensionsDiseaseDisorderDisparitiesDisparityETS Variant Gene 3ETV3ETV3 geneEpidemiological dataEpidemiology dataEpithelial CellsEpithelium of Human Prostate GlandEuropeanExhibitsFRACNFractionationFractionation RadiotherapyGenesGeneticGenetic AlterationGenetic ChangeGenetic defectGenetic mutationGenomeGleason GradeGleason Grade for Prostate CancerGleason ScoreGleason Score for Prostate CancerGleason SumGleason-SCGoalsHaplotypesIncidenceIndividualInvadedKnowledgeLinkMMAC1MMAC1 proteinMalignant NeoplasmsMalignant TumorMalignant neoplasm of prostateMalignant prostatic tumorMass Photometry/Spectrum AnalysisMass SpectrometryMass SpectroscopyMass SpectrumMass Spectrum AnalysesMass Spectrum AnalysisMeasuresMedical centerMeta-AnalysisMethodsModelingMolecularMutated in Multiple Advanced Cancers 1MutationOncogenesOncogenicOrganoidsOutcomePE-1PE1PHTS genePHTS proteinPTENPTEN genePTEN proteinPTEN1Pathway interactionsPatientsPhosphatase and Tensin HomologPhosphatase and Tensin Homolog Deleted on Chromosome 10PopulationProstateProstate CAProstate CancerProstate GlandProstate malignancyProstatectomyProstatic EpitheliumProstatic GlandProstatovesiculectomyProteinsProteomicsRacial GroupRadical ProstatectomyReportingResearch ResourcesResearch SpecimenResourcesSequence AlterationSocio-economic statusSocioeconomic StatusSortingSpecimenStrains Cell LinesSystemTestingTransforming GenesTumor Suppressor ProteinsU.S. MalesUS MenUS maleUnited StatesValidationWorkZFHX3ZFHX3 geneaccess to health careaccessibility of health careaccessibility to health careadvanced diseaseadvanced illnessbiologicbiological specimen archivesbiosample archivebiospecimen archiveblack maleblack manblack mencancer disparitycancer health disparitycancer-related health disparitycandidate identificationcell growthcofactorcohortcomplementationcultured cell linedeath riskdisparities in mortalitydisparities in racedisparity due to racedisparity in cancerearly onsetepidemiologic dataexome sequencingexome-seqgenome editinggenome mutationgenomic alterationgenomic editinghealth care accesshealth care availabilityhealth care service accesshealth care service availabilityhigh riskimprovedinequality due to raceinequity due to raceinnovative technologieslater in lifelater lifemales in Americamales in the U.S.males in the USmales in the USAmales in the United Statesmalignancymenmen in Americamen in the U.S.men in the USmen in the USAmen in the United Statesmortalitymortality disparitymortality ratemortality ratiomortality riskmutated in multiple advanced cancers 1 proteinneoplasm/cancernovelpathwaypatient stratificationphosphatase and tensin homologue on chromosome tenprostate cancer riskrace based disparityrace based inequalityrace based inequityrace disparityrace related disparityrace related inequalityrace related inequityracial disparityracial inequalityracial inequityracial populationracial subgroupracially unequalresistance to therapyresistant to therapyresponsescRNA sequencingscRNA-seqsingle cell RNA-seqsingle cell RNAseqsingle cell expression profilingsingle cell transcriptomic profilingsingle-cell RNA sequencingsocio-economic positionsocioeconomic positionspecimen archivestratified patienttherapeutic resistancetherapy resistanttranscriptomicstreatment resistancetumortumor suppressorvalidationszinc finger homeobox 3
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Full Description

Summary
African American (AA) men have the highest incidence and mortality rate from prostate cancer in the United

States. We recently showed that AA men with low-risk prostate cancer have a two-fold increased risk of death

compared to men of other racial groups. While the causes of this stark disparity are multifactorial, we

hypothesize that low-risk prostate cancer in AA men harbor unique genomic alterations that give rise to more

aggressive prostate cancer. Towards this end, we have performed an initial meta-analysis of existing sequencing

studies and found candidate driver genes associated with ancestry. However, the ability to determine the effect

of these candidates on prostate cancer biology is limited due to the lack of biological cell models from different

ancestral backgrounds. In Aim 1, we will find additional molecular alterations associated with grade using whole

exome sequencing of prostate cancer cases from 300 AA men and 200 men from a European background using

a collection of archived specimens from Boston Medical Center and UCSF. In Aim 2, we will characterize the

transcriptomic and proteomic states of different prostate epithelial cell populations by performing single-cell RNA-

seq and mass spectrometry of organoids derived from AA and EA men. In Aim 3, we will develop new prostate

cell models from AA patients using a conditional reprogramming method. We will then perturb ancestry- and

grade-associated driver genes using CRISPR/Cas9 genome editing and determine whether the functional effects

of these genes are augmented in different ancestral backgrounds. At the conclusion of these studies we will

have expanded our understanding of the molecular pathways are associated with aggressiveness in different

ancestral backgrounds. We will also generate a large resource of prostate cell models from AA men for the

scientific community to investigate prostate cancer disparities. This project will generate substantial knowledge

of the mechanisms that underlie prostate cancer disparities that could ultimately lead to improved treatment of

AA men with prostate cancer and the reduction of cancer health disparities.

Grant Number: 5R01CA248920-05
NIH Institute/Center: NIH

Principal Investigator: Joshua Campbell

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