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Invasion and Angiogenesis in Malignant Gliomas

Invasion and Angiogenesis in Malignant Gliomas
恶性胶质瘤的侵袭和血管生成
批准号:
7367146
负责人:
DAVID ZAGZAG
金额:
$26.28万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-04-01 至 2011-02-28

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): There is a dire need for novel therapy for brain tumors. Diffuse glioma cell invasion into surrounding brain tissue and angiogenesis are fundamental features of gliomas that have not been successfully addressed by conventional therapy to control tumor growth in brain tumor patients. Current aggressive local treatments such as surgery, radiotherapy and chemotherapy are effective at controlling the localized mass of tumor cells in the brain. This success is only temporary, because tumor cells that have already invaded into the surrounding brain and serve as seeds by which the tumor re-grows. The process by which these tumor cells invade into the brain is not well understood. New treatment approaches that are capable to control these invading tumor cells can have a dramatic impact on patient outcome. We have developed assays in vitro and in vivo that allow us to study invading glioma and endothelial cells. Our long-term goal remains to interfere with tumor invasion and angiogenesis to diminish tumor growth. To this end we propose i) to determine mechanisms involved in the migration of both endothelial and glioma cells; and ii) to investigate the mechanism and therapeutic potential of two geldanamycin analogues on glioma in vitro and in vivo. Our proposal seeks to take advantage of new molecular biologic techniques to improve our understanding of this process. Collectively, the proposed experiments will analyze the cellular and molecular pathways necessary for tumor invasion and angiogenesis. Results from these experiments will lead to future strategies designed to inhibit specific molecular components implicated in these critical processes.
期刊论文(11)
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会议论文
HGF upregulates CXCR4 expression in gliomas via NF-kappaB: implications for glioma cell migration.
HGF 通过 NF-kappaB 上调胶质瘤中 CXCR4 的表达:对胶质瘤细胞迁移的影响。
DOI: 10.1007/s11060-010-0111-2
发表时间: 2010-08
期刊: Journal of neuro-oncology
影响因子: 3.9
作者: [Esencay M, Newcomb EW, Zagzag D]
通讯作者: Zagzag D
DOI: 10.1186/1476-4598-9-133
发表时间: 2010-06-01
期刊: Molecular cancer
影响因子: 37.3
作者: [Méndez O, Zavadil J, Esencay M, Lukyanov Y, Santovasi D, Wang SC, Newcomb EW, Zagzag D]
通讯作者: Zagzag D
DOI: 10.1007/s11060-010-0125-9
发表时间: 2010-09
期刊: Journal of neuro-oncology
影响因子: 3.9
作者: [Chen GJ, Karajannis MA, Newcomb EW, Zagzag D]
通讯作者: Zagzag D
Angiogenesis in gliomas: imaging and experimental therapeutics.
神经胶质瘤的血管生成:成像和实验治疗。
DOI: 10.1111/j.1750-3639.2005.tb00119.x
发表时间: 2005
期刊: Brain pathology (Zurich, Switzerland)
影响因子: --
作者: [Gagner,Jean-Pierre, Law,Meng, Fischer,Ingeborg, Newcomb,ElizabethW, Zagzag,David]
通讯作者: Zagzag,David
Identification and molecular characterization of FGFR4 p.G388R variant signaling in cerebellar hemangioblastomas
Identification and molecular characterization of FGFR4 p.G388R variant signaling in cerebellar hemangioblastomas
Novel CXCR4 Therapeutics to Block Bevacizumab-Induced Glioma Dissemination.
Novel CXCR4 Therapeutics to Block Bevacizumab-Induced Glioma Dissemination.
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