Magnetic nanoparticle Immunotherapy against Ovarian Cancer
Magnetic nanoparticle Immunotherapy against Ovarian Cancer
批准号:
8545105
负责人:
STEVEN FIERING
金额:
$28.75万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-08-01 至 2015-07-31
关键词:
AliquotAmericanAntibodiesBindingBiodistributionBiologyBiometryBlood VesselsCCNE1 geneCancer CenterCancer ModelCellsCessation of lifeCharacteristicsCisplatinClinical ResearchData AnalysesDendritic CellsDiagnosisDoseERBB2 geneEffectivenessElementsEndothelial CellsEngineeringEpithelial ovarian cancerEquipmentFolateFolic Acid AntagonistsFreezingFutureGoalsGrowthHeatingHome environmentHumanHyperthermiaImmuneImmune responseImmunityImmunocompetentImmunodeficient MouseImmunosuppressive AgentsImmunotherapyIn VitroIndividualInfiltrationInstructionInterventionIronLeadLearningLeukocytesLocationMagnetismMalignant NeoplasmsMalignant neoplasm of ovaryMediatingModelingMusNanotechnologyOutcomeOvarian CarcinomaPathologyPatientsPatternPreparationReagentRecruitment ActivityRecurrenceResistanceResourcesStagingStromal CellsSupporting CellSurfaceSurvival RateSuspension substanceSuspensionsSystemT-LymphocyteTestingTherapeuticTherapeutic IndexToxicologyTumor BurdenTumor ImmunityVariantWorkXenograft procedureangiogenesisanticancer researchbasecancer cellcancer therapycancer typecell typechemotherapyclinically relevantcombinatorialdesignexperiencehyperthermia treatmentimprovedin vivokillingsmesothelinnanoparticleneoplastic cellnovelovarian neoplasmparticlepre-clinicalpressurereceptorresearch clinical testingresearch studytumortumor xenograftuptake
中文摘要
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英文摘要
PROJECT SUMIMARY (See instructions);
This proposed work will define the potential of treating ovarian cancer with magnetic nanoparticle (mNP)
mediated hyperthermia (mNPHT). It will investigate how best to destroy both tumor cells and leukocytes that
suppress antitumor immunity and support angiogenesis. Studies will be done in vivo in mice using syngeneic
mouse ovarian cancer and human xenografts and in vitro using viable dissociated primary human ovarian
cancer preparations that include tumor cells, leukocytes and endothelial cells. Our extensive experience with
ovarian cancer research will inform the design of mNP selectively targeting tumor and tumor supporting cells.
The hypothesis is that superior therapeutic benefits can be achieved by combining mNP-mediated
thermoablation of tumor cells (including chemoresistant cancer cells) with thermoablation of crucial
immunosuppressive/pro-angiogenic tumor leukocytes and these treatments will synergize with standard
chemotherapies. Aim 1 will determine the impact on tumors of using mNPHT to eliminate tumor-associated
phagocytic leukocytes in immunocompetent murine ovarian cancer models. Aim 2 will use the same murine
tumor models as aim 1 to define the effectiveness of eliminating tumor cells with mNPHT, with or without
tumor-associated leukocyte depletion or suboptimal chemotherapy. Aim 3 will determine the interaction of
differently targeted mNP preparations with freshly dissociated human tumors, using a unique resource of
multiple aliquots of frozen cell suspensions from our large bank of freshly dissociated human ovarian
cancers. Aim 4 will define the effectiveness of mNP-hyperthermia as an individual treatment against human
ovarian cancer xenografts in immunodeficient mice, and will determine how best to apply this treatment in
order to synergize with otherwise ineffective doses of cisplatin.
Throughout this proposal, the reagents, models and experiments have been designed to accomplish the preclinical optimization of mNP-based hyperthermia as a novel intervention against ovarian cancers. These studies will pave the way for subsequent clinical testing of mNPHT in combination with established therapeutic approaches for the treatment of otherwise lethal ovarian cancers.
This project will interact with all other projects and cores: it will draw on the Nanoparticle Core for mNPs, Project 1 will provide ScFv-conjugated particles. Project 2 will test their system in our ovarian tumor models, Project 3 provides the treatment equipment, the Toxicology, Pathology, and Biodistribution Core will assess mNP location and the Biostatistics, Data Analysis, and Computation Core will provide data analysis.
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依托单位:
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财政年份:2010
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财政年份:2010
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资助金额:$18.39万
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财政年份:2009
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项目类别:
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财政年份:2008
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依托单位:
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依托单位:
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-
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负责人:STEVEN FIERING
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依托单位:
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依托单位:
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