Regulation of Hippo Signaling by Src-Family Kinases
Regulation of Hippo Signaling by Src-Family Kinases
批准号:
8764489
负责人:
VALERI VASIOUKHIN
金额:
$35.07万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-09-03 至 2019-08-31
关键词:
AblationActinsAdherens JunctionAdhesionsApplications GrantsBindingBreast Epithelial CellsCadherinsCell AdhesionCell Adhesion MoleculesCell NucleusCell ProliferationCell membraneCell-Cell AdhesionCellsClinical OncologyCultured CellsCytoskeletonDevelopmentE-CadherinEpithelialFutureGene ExpressionGeneticGlial Fibrillary Acidic ProteinHomeostasisHumanIn VitroKnowledgeLATS1 geneLaboratoriesLinkMalignant NeoplasmsMicroRNAsMolecularMusNeoplasm MetastasisNormal tissue morphologyNuclearOncogenicOutputPaperPathway interactionsPatientsPhosphorylationPhosphotransferasesPlayProtein Tyrosine KinaseProteinsProto-OncogenesPublishingRegulationRoleSignal TransductionSignal Transduction PathwaySignaling ProteinSiteSkinSkin CancerSquamous cell carcinomaStem cellsStructureTestingTherapeutic InterventionTissuesTranscriptional ActivationTumor Suppressor GenesTumor Suppressor ProteinsTyrosineTyrosine Phosphorylationadhesion receptoralpha catenincancer stem cellgenetic analysisin vivointerestkeratinocytenoveloutcome forecastpublic health relevanceself-renewalsrc-Family Kinasesstemtranscription factortumortumor initiationtumor progression
中文摘要
描述(申请人提供):细胞粘附受体在肿瘤进展和转移中起关键作用。在正常上皮组织中,细胞粘附紧密,而在高级别肿瘤中,细胞之间的粘附只是松散的,肿瘤周围的细胞表现出明显的细胞-细胞粘附丧失和局部组织侵袭。在高级别肿瘤中,细胞间粘附减少通常是由重要的细胞-细胞粘附蛋白表达减少或完全丧失引起的。E-cadherin显然是这种蛋白中研究得最好的例子,我们对E-cadherin在肿瘤进展和转移中的机制和作用有广泛的了解。我们的实验室一直致力于了解α -连环蛋白的作用和意义,α -连环蛋白是一种细胞-细胞粘附蛋白,将细胞膜上的钙粘蛋白和连环蛋白与肌动蛋白细胞骨架连接起来。在高级别上皮性肿瘤中,α -catenin经常丢失或下调,α -catenin的丢失与转移进展和患者预后不良相关。我们最近已经证明-连环蛋白在鳞状细胞癌中具有重要的肿瘤抑制功能。潜在的分子机制分析揭示了α -catenin与Hippo信号转导通路之间的重要联系。我们提出的初步证据表明,α -连环蛋白在调节表皮干细胞的正常稳态中发挥重要作用。我们还表明,α -catenin的主要信号功能涉及调节src家族酪氨酸激酶的活性。本课题拟研究α -catenin在鳞状细胞癌起始细胞形成中的作用,分析src家族激酶在Hippo信号转导通路调控、肿瘤起始和进展中的作用机制和意义。
英文摘要
DESCRIPTION (provided by applicant): Cell adhesion receptors play a critical role in tumor progression and metastasis. While in normal epithelial tissues cells are tightly adhere, cells in high-grade tumors are only loosely attached to each other, with cells at the tumor periphery displaying prominent loss of cell-cell adhesion and local tissue invasion. Decreased intercellular adhesion in high-grade tumors is often caused by a decreased expression or a complete loss of important cell-cell adhesion proteins. E-cadherin is clearly the best-studied example of such a protein and we have extensive knowledge concerning the mechanisms and the role of E-cadherin in tumor progression and metastasis. Our laboratory has being focused on understanding the role and significance of alpha-catenin, a cell-cell adhesion protein that links cadherin and catenins at the cell membrane with the actin cytoskeleton. Alpha-catenin is often lost or down regulated in high-grade epithelial tumors and loss of alpha-catenin correlates with metastatic progression and poor patient prognosis. We have recently demonstrated that alpha-catenin has an important tumor-suppressor function in Squamous Cell Carcinoma. The analysis of potential molecular mechanisms revealed a prominent connection between alpha-catenin and the Hippo signal transduction pathway. We present preliminary evidence demonstrating an important role of alpha-catenin in regulation of normal homeostasis of epidermal stem cells. We also show that the principal signaling function of alpha-catenin involves regulation of the activit of Src-family tyrosine kinases. In this grant application we propose to investigate the role of alpha-catenin in formation of cancer initiating cells in Squamous Cell Carcinoma and analyze the mechanisms and significance of Src-family kinases in regulation of Hippo signal transduction pathway, tumor initiation and progression.
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会议论文
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海外基金