Role of Synaptojanin 2 in Tumor Cell Invasion
Role of Synaptojanin 2 in Tumor Cell Invasion
批准号:
7232288
负责人:
MARC H SYMONS
金额:
$29.92万
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-06-01 至 2010-04-30
关键词:
AchievementActinsAdaptor Signaling ProteinBindingCancer PatientCell membraneCellsCytoskeletonCytosolDataDrug Delivery SystemsExtracellular Matrix DegradationFilamentGlioblastomaGoalsHydrolysisIn VitroInvasiveLocalizedMalignant - descriptorMediatingMicrofilamentsMolecularMolecular AnalysisMonomeric GTP-Binding ProteinsNeoplasm MetastasisPhosphatidylinositolsPhosphoric Monoester HydrolasesPropertyProteinsRNA InterferenceRegulationResearchRoleSignal PathwaySignal TransductionStructureTestingThinkingTreatment FailureTumor Cell InvasionValidationbasecancer therapycell motilitycrosslinkhuman EMS1 proteinmigrationmutantneoplastic cellnovelreconstitutionsynaptojanin-2synergism
中文摘要
描述(申请人提供):肿瘤细胞的迁移和侵袭特性是转移的关键,这是癌症患者治疗失败的主要原因。然而,在很大程度上控制细胞迁移和侵袭的信号机制仍有待阐明。这项建议的长期目标是阐明由小GTPase rac1激活的信号通路在控制细胞迁移和侵袭中的作用,并利用这些信息来确定癌症治疗的新药物靶点。磷脂酰肌醇磷酸酶Synaptojanin 2(SJ2)是一种新的RAC效应分子,在片状脂膜和内陷的形成以及肿瘤细胞的迁移和侵袭过程中起重要作用。此外,SJ2与Grb2和Cortactin结合,这两种蛋白质与肌动蛋白细胞骨架的控制有关。Grb2激活N-WASP,从而刺激肌动蛋白成核,而Cortactin促进肌动蛋白细丝分支的形成。该应用的目的是确定SJ2在片状脂血症和内陷形成以及肿瘤细胞迁移和侵袭中所起作用的分子机制。这一假设的中心假设是,SJ2通过作用于rac1下游来协调N-WASP和Cortactin的活性,从而促进肿瘤细胞的迁移和侵袭。为了实现本申请的目标,将追求以下特定的目标:1)确定rac1是否通过将SJ2定位于片状脂膜和内膜脂来调节SJ2。2)验证SJ2通过刺激皮质肌动蛋白依赖的肌动蛋白细丝分支而调节细胞迁移和侵袭以及片状脂膜和内脂肪膜形成的假说。3)验证Synaptojanin 2通过调节Grb2/N-WASP依赖的肌动蛋白核化而调节细胞迁移和侵袭以及片状脂膜和隐足细胞形成的假说。对SJ2在片状脂膜和内陷的形成以及肿瘤细胞的迁移和侵袭中的作用的分子分析将极大地扩展我们目前对rac1在恶性转化中的作用的理解。
英文摘要
DESCRIPTION (provided by applicant): The migratory and invasive properties of tumor cells are critical for metastasis, which is the main cause of treatment failure for cancer patients. The signaling mechanisms that control cell migration and invasion largely remain to be elucidated however. The long-term goal of this proposal is to elucidate the signaling pathways that are activated by the small GTPase Rac1 in the control of cell migration and invasion and to use this information to identify novel drug targets for cancer therapy. The phosphatidylinositol phosphatase synaptojanin 2 (SJ2) is a novel Rac effector that is required for the formation of lamellipodia and invadopodia and for tumor cell migration and invasion. Furthermore, SJ2 binds to Grb2 and cortactin, two proteins that have been implicated in the control of the actin cytoskeleton. Grb2 activates N-WASP, which stimulates actin nucleation, whereas cortactin promotes actin filament branch formation. The objective of this application is to determine the molecular mechanisms that underlie the role of SJ2 in lamellipodia and invadopodia formation and tumor cell migration and invasion. The central hypothesis of this proposal is that SJ2 contributes to tumor cell migration and invasion by acting downstream of Rac1 to coordinate the activities of N-WASP and cortactin. To accomplish the goals of this application, the following specific aims will be pursued: 1) To determine whether Rac1 regulates SJ2 by localizing SJ2 to lamellipodia and invadopodia. 2) To test the hypothesis that SJ2 regulates cell migration and invasion and the formation of lamellipodia and invadopodia by stimulating cortactin-dependent actin filament branching. 3) To test the hypothesis that synaptojanin 2 regulates cell migration and invasion and the formation of lamellipodia and invadopodia by regulating Grb2/N-WASP-dependent actin nucleation. The molecular analysis of the functions of SJ2 in the formation of lamellipodia and invadopodia and tumor cell migration and invasion will significantly expand our current understanding of the role of Rac1 in malignant transformation.
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Role of Synaptojanin 2 in Tumor Cell Invasion
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海外基金