Wnt responsive stem cells in the prostate
前列腺中的 Wnt 反应性干细胞
基本信息
- 批准号:9231705
- 负责人:
- 金额:$ 38.25万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2016
- 资助国家:美国
- 起止时间:2016-09-01 至 2019-08-31
- 项目状态:已结题
- 来源:
- 关键词:AddressAdultAndrogensBenign Prostatic HypertrophyBiologicalBiological ProcessBiologyBirthBladderCellsComplexDataDevelopmentDiseaseDorsalDuct (organ) structureEjaculationEmbryoEmbryonic DevelopmentEndocrine GlandsGenesGeneticGrowthGrowth and Development functionHealthcare SystemsHumanIn VitroKnowledgeLabelLeadMaintenanceMalignant NeoplasmsMediatingMolecularMorbidity - disease rateMorphogenesisMusNatural regenerationNeckOrganogenesisPathologyPathway interactionsPatternPerinatalPlayPropertyProstatePubertyResearchRoleSeriesSignal PathwaySignal TransductionStagingStem cellsTestingTissuesUrethraUrogenital Sinusaging populationbasebeta catenindeprivationhuman diseasein vivoinnovationmalemouse modelnovelpluripotencypostnatalprostate lateral lobeprostatitispublic health relevancereproductivereproductive organresponseself-renewalstemtissue repair
项目摘要
DESCRIPTION (provided by applicant): The Prostate gland is an accessory reproductive endocrine organ in males, which expels proteolytic solution in the urethra during ejaculation. In humans, the prostate is located immediately below the base of the bladder surrounding the neck region of the urethra, and is associated with many human diseases, including benign prostate hyperplasia (BPH), prostatitis, and malignancies. The high morbidity of these disorders and related complications are a significant burden on our current healthcare system, and will become even greater for our nation in the coming decades due to a rapid increase of the aging population. Despite the intense research efforts that have been made in past decades, the molecular mechanisms underlying these disorders are still poorly understood. Emerging evidence has shown that stem cells are required to maintain and repair tissues throughout ones' lifetime. Recent studies also demonstrate that certain urogenital sinus cells carry out biological properties to commit to prostate cell fate at the embryonic stage of prostate development. The Wnt signaling pathway plays a critical role in development, morphogenesis, and organogenesis. Wnt growth factors activate different intracellular targets through either the "canonical" or the "non-canonical" pathways. The canonical signaling pathways are mainly mediated through ß-catenin. The Wnt/ß-catenin signaling pathway has been shown to be critical in the development of the prostate at the perinatal stage. Genetic interactions between Wnt/ß-catenin and androgen signaling pathways have been identified in the early development of the prostate. Axin2 is a direct transcriptional target of ß-catenin and is upregulated after activation of Wnt signaling. Recent studies have shown that Axin2 positive cells have stem/progenitor cell properties in a variety of mouse tissues. In this new R01 application, we will use the novel mouse models and other "state-of-the-art" experimental approaches to identify the Wnt/ß-catenin responsive stem/progenitor cells in the prostate, which has never been investigated in the field. Three specific aims are proposed here to test our central hypothesis: Wnt/ß-catenin signaling plays a essential role in prostate development and regeneration through its downstream responsive cells, and that aberrant activation of these responsive cells in the prostate directly contribute t prostate pathology. The proposed study seeks to gain innovative information on prostatic stem/progenitor cells, and may lead to new directions and challenges to current paradigms.
描述(由申请人提供):前列腺是男性的辅助生殖内分泌器官,在射精时排出尿道中的蛋白水解液。在人类中,前列腺位于尿道颈部周围膀胱底部的正下方。 ,并且与许多人类疾病相关,包括良性前列腺增生(BPH)、前列腺炎和恶性肿瘤。这些疾病和相关并发症的发病率很高。这些疾病给我们当前的医疗保健系统带来了巨大的负担,并且由于人口老龄化的迅速增加,未来几十年对我们国家来说将变得更加沉重。新的证据表明,在人的一生中,需要干细胞来维持和修复组织。最近的研究还表明,某些泌尿生殖窦细胞在前列腺发育的胚胎阶段具有决定前列腺细胞命运的生物学特性。 Wnt信号通路在Wnt 生长因子通过“规范”或“非规范”途径激活不同的细胞内靶标。规范信号传导途径主要通过 β-连环蛋白介导。在前列腺的早期发育中已发现 Wnt/ß-连环蛋白和雄激素信号通路之间的遗传相互作用。是 ß-catenin 的直接转录靶标,在 Wnt 信号传导激活后上调。最近的研究表明,Axin2 阳性细胞在多种小鼠组织中具有干/祖细胞特性。在这个新的 R01 应用中,我们将使用新型 R01。小鼠模型和其他“最先进”的实验方法来鉴定前列腺中的 Wnt/ß-连环蛋白反应性干/祖细胞,这在该领域中从未被研究过,这里提出了三个具体目标来测试我们的研究。中央假设:Wnt/β-连环蛋白信号通过其下游反应细胞在前列腺发育和再生中发挥重要作用,并且前列腺中这些反应细胞的异常激活直接导致前列腺病理学。本研究旨在获得有关前列腺的创新信息。干/祖细胞,可能会给当前的范式带来新的方向和挑战。
项目成果
期刊论文数量(0)
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ZIJIE SUN其他文献
ZIJIE SUN的其他文献
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{{ truncateString('ZIJIE SUN', 18)}}的其他基金
A new regulator for Wnt/beta-catenin signaling and prostate tumorigenesis
Wnt/β-连环蛋白信号传导和前列腺肿瘤发生的新调节因子
- 批准号:
9233879 - 财政年份:2016
- 资助金额:
$ 38.25万 - 项目类别:
Androgen Signaling in prostate cancer progression and CRPC development
前列腺癌进展和 CRPC 发展中的雄激素信号传导
- 批准号:
9197890 - 财政年份:2016
- 资助金额:
$ 38.25万 - 项目类别:
A New Mechanism for Castration Resistant Prostate Cancer
去势抵抗性前列腺癌的新机制
- 批准号:
9233878 - 财政年份:2016
- 资助金额:
$ 38.25万 - 项目类别:
Androgen Signaling in prostate cancer progression and CRPC development
前列腺癌进展和 CRPC 发展中的雄激素信号传导
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9233875 - 财政年份:2016
- 资助金额:
$ 38.25万 - 项目类别:
Androgen Signaling in Prostatic Sonic Hedgehog Responsive Cells
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10451616 - 财政年份:2015
- 资助金额:
$ 38.25万 - 项目类别:
Androgen Signaling in Prostatic Sonic Hedgehog Responsive Cells
前列腺 Sonic Hedgehog 反应细胞中的雄激素信号传导
- 批准号:
10295736 - 财政年份:2015
- 资助金额:
$ 38.25万 - 项目类别:
Androgen Signaling in Prostatic Sonic Hedgehog Responsive Cells
前列腺 Sonic Hedgehog 反应细胞中的雄激素信号传导
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10630343 - 财政年份:2015
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Cellular And Molecular Properties Of PINs In Prostate Tumorigenesis
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8791506 - 财政年份:2014
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$ 38.25万 - 项目类别:
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