Interplay Between Stem Cells and Inflammation in Benign Prostatic Hyperplasia
Interplay Between Stem Cells and Inflammation in Benign Prostatic Hyperplasia
批准号:
9166471
负责人:
Douglas William Strand
金额:
$8.1万
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-07-25 至 2018-04-30
关键词:
5 Alpha-Reductase InhibitorAddressAdverse effectsAgeAgingAndrogensAnimalsAntiandrogen TherapyB-LymphocytesBasal CellBenign Prostatic HypertrophyCastrationCd68Cell ProliferationCellsChronicClinicalClinical DataCollaborationsCommunitiesDataDevelopmentEpithelialEpithelial CellsEpitheliumEtiologyFlow CytometryFrequenciesFresh TissueFutureGoalsGrowthHarvestHealthHumanImmunohistochemistryIncidenceInflammationInflammatoryK-Series Research Career ProgramsLaboratoriesLeukocytesLinkMalignant neoplasm of prostateMesenchymeMetabolismMolecularMolecular ProfilingMorbidity - disease rateMusNational Institute of Diabetes and Digestive and Kidney DiseasesNatural regenerationNickelOperative Surgical ProceduresOrganoidsPTPRC genePatient observationPatientsPharmaceutical PreparationsPopulationProliferatingProstateProtocols documentationResearchResearch PersonnelResearch ProposalsResistanceResourcesRiskSamplingSerial PassageSeveritiesSiteSpecimenStagingStem cellsStrategic PlanningSymptomsT-LymphocyteTestingTherapeuticTissue BanksTissuesTranslational Researchbiobankcell typeexperiencehuman diseasehuman stem cellshuman tissueinnovationlower urinary tract symptomsmacrophagemale healthmenmouse modelneoplastic cellnew therapeutic targetnovel strategiespublic health relevancerepositoryself-renewalstemstem cell populationtargeted treatmenttherapy developmenttherapy resistanttissue processingtissue regeneration
中文摘要
项目标题
英文摘要
Project title
Interplay Between Stem Cells and Inflammation in Benign Prostatic Hyperplasia
Project summary
The development of therapies that target the causes rather than the symptoms of benign prostatic hyperplasia
(BPH) requires a novel approach to understanding its cellular etiology. We are building a clinically annotated
fresh tissue repository for interrogating cell-specific fluctuations and molecular signatures. Evidence in mice
and humans demonstrate that androgen-independent stem cells are enriched in the basal epithelium, which is
also the site of the majority of proliferating cells in BPH tissue. It is unclear whether increases in stem cells
or their progeny are causative in BPH. In addition, human prostate volume is directly correlated with chronic
inflammation, and prostate epithelial stem cells are activated by inflammation in mouse models. Accordingly,
this study will build a fresh tissue human BPH repository that will be used to investigate the hypothesis that
inflammation is correlated with stem cell activity in human BPH. Pioneering studies looking for a cell of origin in
prostate cancer have recently produced standardized protocols for harvesting and functionally characterizing
stem cells from human prostate, creating an opportunity to address the connections between inflammatory
cells and epithelial stem activity in BPH. Towards this end, I have leveraged my department's high patient
volume to optimize protocols for fresh tissue collection, stem and inflammatory cell identification by multicolor
flow cytometry, and serial passaging of stem cells in 3D organoid culture. The preliminary data has been
generated solely in my new laboratory and is a natural progression of my K award hypothesis that metabolism
regulates prostate epithelial self-renewal and differentiation. This research proposal is significant because it
provides a cellular etiology for the clinical observation that patients with a large prostate volume display high
inflammation and are resistant to anti-androgen therapy, and it is innovative in its development of a fresh
human prostate biorepository for use of the latest technical advances in flow cytometry and 3D organoid
culture. The development of a human tissue repository will provide the resources and preliminary data for an
R01 application with Early Stage Investigator status in 2 years.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Bedside to bench resources for lower urinary tract research
-
批准号:10517227
-
项目类别:
-
资助金额:$103.93万
-
财政年份:2022
-
负责人:Douglas William Strand
-
依托单位:
Bedside to bench resources for lower urinary tract research
-
批准号:10705120
-
项目类别:
-
资助金额:$102.72万
-
财政年份:2022
-
负责人:Douglas William Strand
-
依托单位:
Notch-mediated 5ARI resistance in human BPH
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批准号:10413136
-
项目类别:
-
资助金额:$37.35万
-
财政年份:2018
-
负责人:Douglas William Strand
-
依托单位:
Notch-mediated 5ARI resistance in human BPH
-
批准号:10183238
-
项目类别:
-
资助金额:$37.86万
-
财政年份:2018
-
负责人:Douglas William Strand
-
依托单位:
CTGF drives voiding dysfunction through expression of collagen in periurethral SRD5A2+ fibroblasts
-
批准号:10700927
-
项目类别:
-
资助金额:$21.8万
-
财政年份:2014
-
负责人:Douglas William Strand
-
依托单位:
CTGF drives voiding dysfunction through expression of collagen in periurethral SRD5A2+ fibroblasts
-
批准号:10264806
-
项目类别:
-
资助金额:$21.8万
-
财政年份:2014
-
负责人:Douglas William Strand
-
依托单位:
CTGF drives voiding dysfunction through expression of collagen in periurethral SRD5A2+ fibroblasts
-
批准号:10022318
-
项目类别:
-
资助金额:$14.17万
-
财政年份:2014
-
负责人:Douglas William Strand
-
依托单位:
Mechanisms of Fatty Acid Metabolism in Prostate Differentiation and Disease
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批准号:9352679
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项目类别:
-
资助金额:$13.75万
-
财政年份:2013
-
负责人:Douglas William Strand
-
依托单位:
Mechanisms of Fatty Acid Metabolism in Prostate Differentiation and Disease
-
批准号:8633558
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项目类别:
-
资助金额:$8.99万
-
财政年份:2013
-
负责人:Douglas William Strand
-
依托单位:
Mechanisms of Fatty Acid Metabolism in Prostate Differentiation and Disease
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批准号:8734409
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项目类别:
-
资助金额:$13.75万
-
财政年份:2013
-
负责人:Douglas William Strand
-
依托单位:
Mechanisms of Fatty Acid Metabolism in Prostate Differentiation and Disease
-
批准号:8928602
-
项目类别:
-
资助金额:$13.75万
-
财政年份:2013
-
负责人:Douglas William Strand
-
依托单位:
CTGF drives voiding dysfunction through expression of collagen in periurethral SRD5A2+ fibroblasts
-
批准号:9921108
-
项目类别:
-
资助金额:$23.31万
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财政年份:--
-
负责人:Douglas William Strand
-
依托单位:
海外基金