Targeting androgen receptor signaling in prostate cancer in men with African ancestry
Targeting androgen receptor signaling in prostate cancer in men with African ancestry
批准号:
10327764
负责人:
Changmeng Cai
金额:
$15.25万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-09-28 至 2024-08-31
关键词:
AR geneAddressAffectAfricanAfrican AmericanAmericanAndrogen ReceptorAndrogen TherapyAndrogensApoptoticBasic ScienceBiologicalBostonCAG repeatCancer CenterCancer EtiologyCancer PatientCellsCessation of lifeClinicalCombined Modality TherapyCritical PathwaysDNA DamageDNA Sequence RearrangementDana-Farber Cancer InstituteDependenceDevelopmentDoseEuropeanGeneticGenetic PolymorphismGenetic TranscriptionGenomicsGlutamineGrantHigh PrevalenceKDM1A geneLeadLengthLigandsMalignant neoplasm of prostateMassachusettsModelingMolecular TargetMutationN-terminalNuclearOutcomePathway interactionsPatientsPlayPopulationProteinsReceptor SignalingResearchRisk FactorsRoleTestingTherapeuticTranslational ResearchUniversitiescancer health disparitycancer initiationmenpolyglutamineprogramsprostate cancer cellprostate cancer cell lineprostate cancer modelracial disparityrepairedresponsetargeted agenttargeted treatmenttranscription factortumor progression
中文摘要
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英文摘要
ABSTRACT
Prostate cancer (PCa) is the second leading cause of cancer-related death in American men. Although men with
European ancestry (EA) still represent the largest population of PCa patients, men with African ancestry (AA)
are disproportionately affected by PCa with higher prevalence and worse outcomes. Androgen receptor (AR), a
ligand-dependent nuclear transcription factor, plays a pivotal role in PCa development, and there are well-
established genetic differences in the AR gene and associated pathways between EA versus AA men. However,
it remains unclear how these genetic differences alter AR interaction with associated proteins, and their potential
role in PCa development and response to AR targeted therapies. In this study, we hypothesize that differences
in AR signaling contribute to the biological differences between PCa in AA versus EA men, and that PCa in AA
men may have distinct AR-dependencies and be vulnerable to therapies that combine AR-targeted therapies
with other targeted agents. To test these hypotheses, Aim 1 will assess the effect of androgen stimulation on
PCa cells from AA versus EA patients, and in isogenic cells reflecting the genetic difference of AR. Aim 2 will
identify vulnerabilities generated in response to AR-targeted therapies in AA versus EA PCa models.
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海外基金