Coordinating Cell Killing by Communication: Biological Control and Cancer Therapy
Coordinating Cell Killing by Communication: Biological Control and Cancer Therapy
批准号:
7879518
负责人:
LINGCHONG YOU
金额:
$20.84万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-08-16 至 2012-07-31
关键词:
AddressBacteriaBehaviorBiologicalBiological ModelsBiomedical ResearchCell CommunicationCell DensityCellsCessation of lifeCommunicationCommunitiesComplexComputing MethodologiesConsensusContainmentControlled StudyDataDecision MakingDevelopmentEcosystemEffectivenessEngineeringEnvironmentEscherichia coliEvaluationFoundationsGene DeliveryGene ExpressionGenesGeneticGoalsGrowthIn VitroLawsLeadLifeLiquid substanceLogicMalignant NeoplasmsMedicalMethodsMicrobial BiofilmsModelingOutcomePerformancePhasePopulationPopulation DensityPopulation DynamicsProteinsPublic HealthResearchResearch PersonnelSignal TransductionSignaling MoleculeSimulateSoftware ToolsSolidSolid NeoplasmSpecificityStudy modelsSystemTestingTherapeuticTherapeutic Effectbiological systemscancer therapycell killingcell typedesignengineering designgenetic elementinnovationinsightkillingsmathematical modelmicrobial communitymodel designmutualismneoplastic cellpractical applicationprogramsquorum sensingskillsspatiotemporalsuccesssynthetic biologytooltumor
中文摘要
描述(由申请人提供):癌症治疗需要开发多种治疗策略。为此,工程细菌提供了有效递送和表达具有治疗效果的基因以及选择性肿瘤靶向的希望。为了充分发挥细菌的治疗潜力,我们需要在多个层面上克服技术障碍。其中包括开发一个遗传元件工具箱,这些元件可以拼凑在一起以实现治疗功能,并更好地理解设计原理,从而能够精确控制实体瘤复杂微环境中的细菌动力学。为了应对这些挑战,本申请的目的是使用细菌的“群体感应”模块来协调不同环境中的细菌行为(生命,死亡,空间聚集)。群体感应(Quorum sensing)是细菌感知并响应其种群密度变化的一种机制。建立在强大的初步数据,拟议的研究将集中在设计,建模,实施和表征两个合成细菌多细胞系统在大肠杆菌。第一个系统(目标1)。捕食者-被捕食者系统)将试图对两个细菌种群的相互作用进行编程,这两个细菌种群相互调节它们的基因表达;电路逻辑和动力学类似于被充分研究的捕食者-被捕食者生态系统。第二个(目标2)。靶向共有回路)将通过两个通信细菌群体的协调决策来编程细菌以高特异性靶向肿瘤细胞。这项研究是创新的,因为它扩展了合成生物学的基本概念和设计方法,以解决癌症治疗的紧迫问题。其结果将通过为具有高度可靠行为的工程细菌的治疗应用奠定坚实的基础而产生重大影响。具体而言,预期成果包括:(1)一系列特征良好的遗传元件、模块和系统;(2)对复杂环境(如实体瘤)中细胞动力学稳健控制的基本设计规律的深入了解;(3)经过全面测试的建模工具和方法。所有这些都可以应用于拟议系统之外的系统,并将与生物医学研究界共享。与公共卫生的相关性:这项研究将填补限制工程设计策略应用于癌症靶向细菌开发的重要空白。这种方法将提供有效和安全的癌症治疗所需的极高的靶向选择性和细菌遏制效率。
英文摘要
DESCRIPTION (provided by applicant): Cancer treatment requires development of diverse therapeutic strategies. To this end, engineered bacteria offer promise for efficiently delivering and expressing genes with therapeutic effects and for selective tumor targeting. To fully realize bacteria's therapeutic potential, we need to overcome technological hurdles at multiple levels. These include development of a toolbox of genetic elements that can be pieced together to carry out therapeutic functions and a better understanding of design principles that will enable precise control of bacterial dynamics in the complex micro-environments of solid tumors. To address these challenges, the objective of this application is to use bacterial "quorum sensing" modules to coordinate bacterial behavior (life, death, spatial aggregation) in diverse settings. Quorum sensing is a mechanism by which bacteria sense and respond to changes in their population density. Built upon strong preliminary data, the proposed research will focus on design, modeling, implementation, and characterization of two synthetic bacterial multicellular systems in Escherichia coli. The first system (Aim 1. a predator-prey system) will attempt to program the interaction of two bacterial populations that mutually regulate their gene expression; the circuit logic and dynamics resemble well-studied predator-prey ecosystems. The second (Aim 2. a targeted consensus circuit) will program bacteria to target tumor cells with high specificity through coordinated decision making by two communicating bacterial populations. The proposed research is innovative, because it extends basic concepts and design methods of synthetic biology to address the pressing issue of cancer therapy. Its outcome will have significant impact by setting a solid foundation for engineering bacteria with highly reliable behavior for therapeutic applications. In particular, expected outcomes include (1) a repertoire of well-characterized genetic elements, modules, and systems, (2) insights into fundamental design laws for robust control of cellular dynamics in complex environments such as solid tumors, and (3) thoroughly tested modeling tools and methods. All of these can be applied in systems beyond the proposed ones and will be shared with the biomedical research community. Relevance to Public Health: The proposed research will fill the important gap that limits the application of engineering design strategies to the development of cancer-targeting bacteria. This approach will offer the extremely high targeting selectivity and bacterial containment efficiency needed for effective and safe cancer therapy.
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DOI:
10.1016/j.copbio.2009.08.006
发表时间:
2009-08
期刊:
CURRENT OPINION IN BIOTECHNOLOGY
影响因子:
7.7
作者:
[Pai, Anand, Tanouchi, Yu, Collins, Cynthia H., You, Lingchong]
通讯作者:
You, Lingchong
DOI:
10.1371/journal.pcbi.1000167
发表时间:
2008-08-29
期刊:
PLoS computational biology
影响因子:
4.3
作者:
[Tanouchi Y, Tu D, Kim J, You L]
通讯作者:
You L
DOI:
10.1021/sb300044r
发表时间:
2012-09-21
期刊:
ACS SYNTHETIC BIOLOGY
影响因子:
4.7
作者:
[Riccione, Katherine A., Smith, Robert P., Lee, Anna J., You, Lingchong]
通讯作者:
You, Lingchong
DOI:
10.1007/978-1-61779-412-4_19
发表时间:
2012
期刊:
Methods in molecular biology
影响因子:
--
作者:
[Stephen Payne;R. P. Smith;L. You]
通讯作者:
Stephen Payne;R. P. Smith;L. You
DOI:
10.1007/978-1-61779-833-7_11
发表时间:
2012
期刊:
Methods in molecular biology (Clifton, N.J.)
影响因子:
--
作者:
[Song,Hao, You,Lingchong]
通讯作者:
You,Lingchong
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Targeted control of self-transmissible plasmids by using engineered interfering plasmids
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Targeted control of self-transmissible plasmids by using engineered interfering plasmids
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Targeted control of self-transmissible plasmids by using engineered interfering plasmids
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Tradeoffs between fitness costs and transfer rates in horizontal gene transfer
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Dynamics of horizontal gene transfer in response to antibiotic treatment
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资助金额:$37.84万
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Temporal E2F Dynamics and Cell-Fate Decisions in Single Mammalian Cells
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批准号:8631365
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Temporal E2F Dynamics and Cell-Fate Decisions in Single Mammalian Cells
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A synthetic biology approach to analyze evolution of programmed bacterial death
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A synthetic biology approach to analyze evolution of programmed bacterial death
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Analyzing inoculum effect and optimal design of antibiotic treatment
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Post-antibiotic effect and design of optimal antibiotic dosing protocols
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Administrative supplement to purchase a sequencing equipment
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Evolutionary dynamics of combinational antimicrobial treatments
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Analyzing inoculum effect and optimal design of antibiotic treatment
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财政年份:2007
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依托单位:
Coordinating Cell Killing by Communication: Biological Control and Cancer Therapy
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批准号:7142537
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资助金额:$22.09万
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