Prostate Cancer Recurrence: models and mechanisms
Prostate Cancer Recurrence: models and mechanisms
批准号:
8386435
负责人:
Sarki A. Abdulkadir
金额:
$37.24万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-08-01 至 2017-05-31
关键词:
AblationAllelesAndrogen ReceptorAndrogensAnimalsAutomobile DrivingBasal CellCancer RelapseCastrationCellsClinicalCompetenceDevelopmentDiphtheria ToxinEnvironmentEpithelial CellsEpitheliumGene MutationGoalsHomeodomain ProteinsHumanLeadMalignant NeoplasmsMalignant neoplasm of prostateMediatingModelingMolecularMolecular TargetMonitorMusMutationNatural regenerationOncogenesOncogenicOutcomes ResearchPathway interactionsPolycombPopulationProstateProstaticProstatic NeoplasmsPublic HealthRecurrenceRecurrent tumorRelapseRelative (related person)ReporterResistanceRoleRosaStem cellsSubfamily lentivirinaeTestingTherapeutic InterventionTissue RecombinationTranscription Repressor/CorepressorTransgenic MiceTumor Suppressor GenesTumor Suppressor Proteinscancer cellcancer recurrencecell typedefined contributionin vivonovel strategiesnovel therapeutic interventionstemstem cell populationtumortumorigenesis
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): A major clinical problem in prostate cancer is that of tumor recurrence following initial apparently successful therapy. It is widely believed that recurrent tumors may arise from a small number of "cancer stem-like cells" that survive the initial therapeutic intervention and which have the capacity to regenerate the tumor. However, this idea has been difficult to test in vivo without manipulation of the cancer cells outside their
native environment in the animal. Here we propose a lineage-tracing strategy to examine the competence of specific prostate epithelial cell types ("castration-resistant Nkx3.1-expressing cells or CARNs" and Bmi1+ cells) to regenerate tumors following androgen ablation in mice (Aim 1). We will further examine whether recurrent tumors driven by specific oncogenic mutations preferentially arise from particular cell populations of stem-like cells within a regressed tumor and the role of the androgen receptor (Aim 2). Finally, we will employ lineage ablation of specific cell types within a regressed tumor to assess the relative contributions of specific stem-like cells (CARNs and Bmi1+ cells) to prostate cancer relapse (Aim 3). In these studies will use novel approaches to define the significance of specific prostate cell types in tumor relapse following androgen ablation. This proposal if successful will have a major impact on our understanding of the cellular origins of recurrent prostate cancer and will facilitate effors aimed at successfully eradicating the tumor.
PUBLIC HEALTH RELEVANCE: The studies outlined in the proposal are directly relevant to the question of the mechanisms underlying the development of recurrence in prostate cancer. The problem of recurrence after therapy is a major public health concern. By identifying the cellular origins of recurrent prostate cancer and investigating the underlying molecular mechanisms, our studies can yield new therapeutic approaches and molecular targets for treating recurrence.
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