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Replacement of animal models for tumour biology with a multifunctional microfluidic-based approach

Replacement of animal models for tumour biology with a multifunctional microfluidic-based approach
用多功能微流体方法替代肿瘤生物学动物模型
批准号:
G1100600/1
负责人:
John Greenman
金额:
$57.45万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2012
资助国家:
英国
项目状态:
已结题
起止时间:
2012 至 --

项目摘要

项目成果

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中文摘要
翻译
该项目的目的是设计和优化一种新型的微流控装置,在这种装置中,人类肿瘤组织的小活检组织可以保持存活,用药物治疗,并通过适当的分析技术在下游测试效果。这种人类系统将能够取代制药行业对新药和药物组合的一般性测试,这些测试在动物模型上只能很好地复制人类的生理和代谢。此外,还可以对任何组织类型的正常组织和病变组织进行活检,从而可以轻松评估特异性治疗反应和非特异性副作用。越来越多的证据表明,许多癌症患者,特别是卵巢癌和胰腺癌患者的血液凝固事件发生率增加;这些凝块可能是致命的。还有证据表明,当患者接受化疗时,肿瘤细胞被破坏,细胞碎片的释放进一步增加了凝血的风险。在该项目中,我们建议设计一种设备,允许使用人类卵巢肿瘤模型分析这些凝血途径。三个分析模块将被集成到一个装置上,在该装置上孵育组织样品,从而可以监测不同类型的生物反应,包括表达基因、细胞表面成分和分泌产物的变化。这些不同类型的分析模块展示了这种新平台技术的广泛适用性和潜力。此外,卵巢癌的死亡率相对较高,存活率在过去20年中没有实质性提高。新技术不仅将取代大量已证明价值有限的传统动物试验,而且还能够对肿瘤样本进行多次试验,这是肿瘤样本的一个非常接近的代表性,在组织已经经受药物或其它测试条件之后,意味着可以产生关于任何个体肿瘤的大量信息。当在诊断时获得这些数据时,这些数据将对临床医生非常有用。预期的治疗策略可以根据患者量身定制,如果没有治疗似乎会产生任何治疗效果,则可以与患者讨论是否有机会将姑息治疗作为首选,同时保持最佳的生活质量。
英文摘要
The aim of the project is to design and optimise a novel microfluidic device in which small biopsies of human tumour tissue can be kept alive, treated with drugs and the effects tested downstream by appropriate analysis techniques. This human system will be able to replace the generalised testing of new drugs and combinations of drugs by the pharmaceutical industry, on animal models that only poorly replicate the physiology and metabolism of human beings. In addition it will be possible to test biopsies of both normal and diseased pieces of any tissue type so that both specific therapeutic responses, as well as non-specific side-effects can easily be assessed.There is growing evidence that patients with many cancers, particularly ovarian and pancreas suffer with an increased occurrence of blood clotting events; these clots can be lethal. There is also evidence that when patients undergo chemotherapy and the tumour cells are destroyed the release of cell debris further increases the risk of clotting. In the project we propose to design a device that allows analysis of these clotting pathways, using a human ovarian tumour model. Three analysis modules will be integrated into a device on which a sample of tissue is incubated, allowing different types of biological response to be monitored, including changes in the expressed genes, cell surface components and secreted products. These distinct types of analysis module demonstrate the widespread applicability and potential of this new platform technology. Furthermore, ovarian cancer has a relatively high mortality with survival rates not improving substantially over the past two decades.Not only will the new technology replace a large number of conventional animal tests, of limited proven value, but the capability of undertaking multiple tests on a tumour sample, that is an extremely close representation of the mass from which it came, after the tissue has been subjected to a drug or other test condition, means that a large amount of information can be generated on any individual tumour. Such data will be extremely useful for the clinician when obtained at the time of diagnosis. The intended treatment strategy can be tailored to the patient, and where no treatment appears to give any therapeutic effect, this can be discussed with the patient opening the opportunity for palliative care to be the preferred choice, whilst maintaining the best quality of life.
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