Role of Prostatic Fibrosis in BPH/LUTS Development & Symptomology
Role of Prostatic Fibrosis in BPH/LUTS Development & Symptomology
批准号:
8049846
负责人:
Jill A. Macoska
金额:
$29.84万
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:
2010-09-30 至 2012-07-31
关键词:
AblationAffectAgingAmericanAndrogensArchitectureAreaCellsClinicalDevelopmentEngineeringExhibitsExtracellular MatrixFacultyFeasibility StudiesFibrosisFunctional disorderGenitourinary systemHumanLaboratoriesMeasuresMechanicsMedicalMedicineMichiganMusMuscle RigidityMyofibroblastObesityObstructionPathologyPatientsProstateProstaticProstatic DiseasesProteinsRoleSchoolsSmooth MuscleTestingTherapeuticTissuesTransgenic MiceUniversitiesUrethraUrologic Diseasesbasedesignflexibilityin vitro testingin vivolower urinary tract symptomsmenmultidisciplinarynovel strategiespublic health relevancesenescencesoft tissuetherapeutic targeturinary
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The proposed planning Center brings together a multidisciplinary team to explore a new paradigm that incorporates fibrosis as a contributing factor to urinary dysfunction and lower urinary tract symptoms (LUTS) development and progression. This team comprises faculty from two schools within the University of Michigan - Medicine and Engineering - that provides broad expertise in laboratory-based studies of urologic disease (Macoska), clinical expertise in treating prostate disease (Hollingsworth) and genitourinary pathology (Kunju), and in soft tissue mechanics (Arruda). The Center team has designed feasibility studies that employ quantitative approaches designed to measure fibrotic changes in human and mouse tissues and cells and to assess whether these fibrotic changes alter tissue rigidity/stiffness and thereby contribute to urinary dysfunction. These studies will test the specific hypothesis that extracellular matrix (ECM) remodeling by accumulating myofibroblasts in the aging prostate effectively generates a fibrotic prostate tissue architecture that increases tissue rigidity and reduces urethral flexibility, resulting in urinary flow obstruction and LUTS. These studies are organized into three Specific Aims:
Specific Aim 1 will determine whether tissues from the peri-urethral area of the human prostate in aging men and particularity those with LUTS demonstrate changes in the extracellular matrix (ECM) consistent with fibrosis, and whether these changes are associated with increased tissue ' mechanical rigidity and stiffness.
Specific Aim 2 will elucidate which proteins secreted by aging prostate stroma contribute to myofibroblast differentiation and ECM dysfunction in vitro, and test therapeutic approaches to inhibit or reverse these changes.
Specific Aim 3 will determine whether Senescence-Accelerated Mouse Prone 6 (SAMP6) and/or KC Transgenic mice exhibit changes in the ECM consistent with fibrosis, whether these changes are associated with increased tissue mechanical rigidity and stiffness, whether these changes affect urinary flow, and whether this pathology is exacerbated by obesity in vivo.
If successful, the results of these studies will open the door to a new approach to effectively treat LUTS especially among men who cannot tolerate or fail to respond to current medical therapeutic approaches.
PUBLIC HEALTH RELEVANCE: Lower urinary tract symptoms (LUTS) are a costly and critically progressive medical problem for millions of aging American men. Current therapeutic approaches for LUTS are focused on the ablation of androgen or smooth muscle activity, but these are not effective for all patients. This application seeks to determine whether a new class of therapeutics targeting tissue fibrosis may be developed to treat LUTS.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Persistence of an IL-4/IL-13 autocrine loop promotes fibrosis-mediated urinary voiding dysfunction
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批准号:10022319
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项目类别:
-
资助金额:$9.03万
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财政年份:2014
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负责人:Jill A. Macoska
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依托单位:
Persistence of an IL-4/IL-13 autocrine loop promotes fibrosis-mediated urinary voiding dysfunction
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批准号:10700930
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项目类别:
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资助金额:$12.69万
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财政年份:2014
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负责人:Jill A. Macoska
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依托单位:
Persistence of an IL-4/IL-13 autocrine loop promotes fibrosis-mediated urinary voiding dysfunction
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批准号:10264807
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项目类别:
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资助金额:$12.7万
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财政年份:2014
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负责人:Jill A. Macoska
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依托单位:
Fibrosis-Associated Urinary Gene Transcripts for LUTS Detection and Treatment
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批准号:8738645
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项目类别:
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资助金额:$21.32万
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财政年份:2013
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负责人:Jill A. Macoska
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依托单位:
Fibrosis-Associated Urinary Gene Transcripts for LUTS Detection and Treatment
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批准号:8486921
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项目类别:
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资助金额:$21.66万
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财政年份:2013
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负责人:Jill A. Macoska
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依托单位:
Society for Basic Urologic Research Fall Symposium 2012
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批准号:8453755
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项目类别:
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资助金额:$1.0万
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财政年份:2012
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负责人:Jill A. Macoska
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依托单位:
Role of Prostatic Fibrosis in BPH/LUTS Development & Symptomology
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批准号:8150959
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项目类别:
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资助金额:$29.84万
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财政年份:2010
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负责人:Jill A. Macoska
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依托单位:
Shared Resource Core
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批准号:10007612
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项目类别:
-
资助金额:$14.88万
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财政年份:2010
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负责人:Jill A. Macoska
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依托单位:
Genomics Core
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批准号:10490401
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项目类别:
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资助金额:$13.19万
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财政年份:2010
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负责人:Jill A. Macoska
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依托单位:
Genomics Core
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批准号:10327770
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项目类别:
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资助金额:$13.49万
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财政年份:2010
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负责人:Jill A. Macoska
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依托单位:
Genomics Core
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批准号:10704706
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项目类别:
-
资助金额:$12.97万
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财政年份:2010
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负责人:Jill A. Macoska
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依托单位:
PTEN- and EGFR-Dependence of CXCL12-Mediated Proliferation in the Aging Prostate
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批准号:7849061
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项目类别:
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资助金额:$32.5万
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财政年份:2008
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负责人:Jill A. Macoska
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依托单位:
Microarray Core
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批准号:7662390
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项目类别:
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资助金额:$6.84万
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财政年份:2008
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负责人:Jill A. Macoska
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依托单位:
PTEN- and EGFR-Dependence of CXCL12-Mediated Proliferation in the Aging Prostate
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批准号:8077425
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项目类别:
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资助金额:$32.18万
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财政年份:2008
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负责人:Jill A. Macoska
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依托单位:
PTEN- and EGFR-Dependence of CXCL12-Mediated Proliferation in the Aging Prostate
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批准号:7666925
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项目类别:
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资助金额:$32.83万
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财政年份:2008
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负责人:Jill A. Macoska
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依托单位:
Microarray Core
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批准号:7483085
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项目类别:
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资助金额:$3.69万
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财政年份:2007
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负责人:Jill A. Macoska
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依托单位:
University of Michigan O'Brien Center for Urology Research
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批准号:7500606
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项目类别:
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资助金额:$21.36万
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财政年份:2007
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负责人:Jill A. Macoska
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依托单位:
AFFYMETRIX
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批准号:7304481
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项目类别:
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资助金额:$13.0万
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财政年份:2006
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负责人:Jill A. Macoska
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依托单位:
A Model System for Human Prostate Tumorigenesis
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批准号:6469499
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项目类别:
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资助金额:$15.06万
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财政年份:2002
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负责人:Jill A. Macoska
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依托单位:
A Model System for Human Prostate Tumorigenesis
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批准号:6669098
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项目类别:
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资助金额:$15.06万
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财政年份:2002
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负责人:Jill A. Macoska
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依托单位:
海外基金