USING VIRAL NANOPARTICLES TO TARGET CANCER
USING VIRAL NANOPARTICLES TO TARGET CANCER
批准号:
7193491
负责人:
MARIANNE MANCHESTER
金额:
$72.65万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-03-01 至 2010-01-31
关键词:
Animal ModelBindingBiochemicalBiologicalBiological AvailabilityBiologyBiopsyCellsChemicalsChemistryChimera organismContractsCowpea Mosaic VirusesDevelopmentEarly DiagnosisGenesGenomeGoalsImageIn VitroInsect VirusesInvasiveKnowledgeLabelLaboratoriesLeadMalignant NeoplasmsMolecular BiologyMosaic VirusesNanotechnologyNational Cancer InstituteOperative Surgical ProceduresPeptidesPlant VirusesProcessPropertyProteinsQuality of lifeRelative (related person)Research PersonnelSolutionsStructureSurfaceSystemTechniquesTechnologyTestingTherapeutic AgentsViralVirusWorkbasecancer therapycellular targetingchemical geneticscostdesignexperienceimprovedin vivomultidisciplinarynanoparticleneoplastic cellnovelparticleprogramsresearch studysensortumortumor progressiontumorigenesisuptake
中文摘要
描述(由申请人提供):纳米技术为癌症的早期检测和治疗带来了巨大的希望。在没有活检、手术或其他侵入性技术的情况下检测和跟踪癌症的发生和进展的能力应该会降低成本和提高生活质量。该提案的目标是开发病毒纳米颗粒(VNPs)作为体内肿瘤靶向和成像剂组合的平台。我们的多学科团队结合了分子生物学,结构,化学和体内生物学来解决这个问题。在这项建议中,我们将研究两个良好的特点病毒:植物病毒,豇豆花叶病毒(CPMV)和昆虫病毒,鸡舍病毒(FHV)。在共同研究者的实验室中开发的FHV和CPMV的结构、功能、组装、基因组包装、化学附着和体内生物利用度的累积知识使这些病毒成为这种平台开发的理想候选者。我们将在体外和体内测试肿瘤特异性VNPs攻击肿瘤细胞的能力,并研究VNPs进入细胞的机制。我们还将在颗粒内包装抗肿瘤化合物和抑制基因,以促进肿瘤破坏。最后,我们将测试我们的VNPs在体内检测和破坏肿瘤的能力。这些研究将为改进肿瘤靶向和成像纳米技术的发展做出重大贡献。
英文摘要
DESCRIPTION (provided by applicant): Nanotechnology holds great promise for the early detection and treatment of cancer. The ability to both detect and follow the initiation and progression of cancer without biopsy, surgery, or other invasive techniques should lead to lower costs and higher quality of life. The goal of this proposal is to develop viral nanoparticles (VNPs) as platforms for combination tumor targeting and imaging agents in vivo. Our multidisciplinary team combines molecular biology, structure, chemistry and in vivo biology to attack this problem. In this proposal we will study two well-characterized viruses: a plant virus, cowpea mosaic virus (CPMV); and an insect virus, flockhouse virus (FHV). The accumulated knowledge of the structure, function, assembly, genome packaging, chemical attachment, and in vivo bioavailability of FHV and CPMV, developed in the co-investigators' laboratories, makes these viruses ideal candidates for such platform development. We will test the ability of tumor-specific VNPs to attack tumor cells in vitro and in vivo, and study mechanisms of uptake of VNPs into cells. We will also package anti-tumor compounds and inhibitory genes inside the particles to facilitate tumor destruction. Finally we will test the ability of our VNPs to detect and destroy tumors in vivo. These studies will make a significant contribution to the development of improved tumor targeting and imaging nanotechnologies.
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