Microfabrication Tools for In Vitro Monitoring of Cancer Cell Metabolism
Microfabrication Tools for In Vitro Monitoring of Cancer Cell Metabolism
批准号:
7366975
负责人:
Alexander Revzin
金额:
$19.33万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-06-01 至 2010-05-31
关键词:
AerobicAntineoplastic AgentsBiosensing TechniquesBiosensorCellsConditionCultured CellsCytotoxic agentDetectionDevicesDiagnosticElectrodesEnergy MetabolismEnvironmentEnzymesEthylene GlycolsFutureGelGlassGliomaGlucoseGlycolysisGoalsGoldHydrogelsHypoxiaIn VitroLightMalignant NeoplasmsMalignant neoplasm of brainMammalian CellMeasuresMetabolicMetabolismMicroelectrodesMicrofabricationMicrofluidic MicrochipsMitogen-Activated Protein KinasesMolecularMonitorNeoplasm MetastasisNormal tissue morphologyNutrientOrganOxygen measurement, partial pressure, arterialPharmaceutical PreparationsPhysiologicalPrincipal InvestigatorProductionSignal Transduction PathwayStaining methodStainsSystemTechnologyTherapeuticThinkingU-0126Workcancer cellcancer therapyconceptdesigndrug efficacyethylene glycolextracellularglucose metabolismglucose oxidasekinase inhibitorprogramsresearch studyresponsesensorsmall moleculetherapy designtooltool developmenttumor
中文摘要
描述(申请人提供):细胞和器官的生理或病理生理状态反映在它们的能量代谢中。例如,在肿瘤中几乎总是可以观察到葡萄糖代谢的偏差。癌细胞的能量代谢与正常组织明显不同,即使在有氧条件下,癌细胞的糖酵解和随后的乳酸产生也更加突出。越来越多的癌症治疗策略被设计成针对代谢偏差,使葡萄糖或乳酸等能量代谢物的水平潜在地与药物疗效相关。这项提议的目标是开发一个芯片实验室平台,用于体外监测候选药物对癌细胞能量代谢的影响。拟议的平台将在一个微型制造设备中将小组胶质瘤(脑癌)细胞与微型葡萄糖生物传感器紧密结合,在这种设备中,细胞微环境可以被精确定义和轻松调制。该平台将用于:1)在胶质瘤细胞培养中建立模拟肿瘤的微环境条件(如低氧、酸性、营养限制);2)用能量代谢中心的激酶信号转导通路的药物抑制剂挑战细胞;以及3)监测局部细胞外葡萄糖水平。因此,细胞培养/生物传感器平台将连接肿瘤微环境、能量代谢和抗癌药物疗效,并将有助于描绘使癌细胞更容易接受治疗的条件。这项拟议的技术将是开发治疗性抗癌药物的有价值的工具,并将有助于阐明癌细胞代谢适应的分子方面。
英文摘要
DESCRIPTION (provided by applicant): The physiological or pathophysiological state of cells and organs is reflected in their energy metabolism. For example, deviations in glucose metabolism is almost always observed in tumors. The energy metabolism of cancer cells differs strikingly from normal tissue with glycolysis and subsequent lactate production being much more prominent in cancer cells, even under aerobic conditions. Increasingly, therapeutic strategies for cancer treatment are designed to target metabolic deviations, making levels of energy metabolites such glucose or lactate potential correlates of drug efficacy. The goal of this proposal is to develop a lab-on-chip platform for in vitro monitoring of the effects of drug candidates on energy metabolism of cancer cells. The proposed platform will intimately integrate small groups of glioma (brain cancer) cells with miniature glucose biosensors in a microfabricated device, where the cellular microenvironment can be precisely defined and easily modulated. This platform will be used to: 1) establish tumor-mimicking microenvironment conditions (e.g. hypoxic, acidic, nutrient-limiting) in glioma cell cultures; 2) challenge the cells with pharmacological inhibitors of kinase signal transduction pathways central in energy metabolism; and 3) monitor local extracellular glucose levels. Thus the cell culture/biosensor platform will connect tumor microenvironment, energy metabolism and anti-cancer drug efficacy, and will help to delineate conditions making cancer cells more susceptible to therapy. The proposed technology will be a valuable tool for the development of therapeutic anti-cancer agents, and will help illuminate molecular aspects of metabolic adaptation of cancer cells.
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