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药物研发中的转移模型。

Models of metastasis in drug discovery.

作者信息

Talmadge James E

机构信息

University of Nebraska Medical Center, Omaha, NE, USA.

出版信息

Methods Mol Biol. 2010;602:215-33. doi: 10.1007/978-1-60761-058-8_13.

Abstract

By definition, animal models provide only an approximation of clinical reality. One reason for this, for example, is that although metastases are the primary cause of mortality from neoplasia, by are rarely considered a target in drug discovery and development. Due to the impact of metastasis on clinical disease, we posit that metastasis should be considered in drug discovery, in addition, to more traditional biologic concepts, including drug pharmacology and toxicity. Drug discovery and developmental studies can incorporate orthotopic and spontaneous metastasis models (syngeneic and xenogeneic) with their inherent host-tumor microenvironmental interactions, in addition to confirmatory autochthonous and/or genetically engineered models (GEMs). This requires a rational and hierarchical approach using models of metastatic disease optimally using resected, orthotopic primary tumors and clinically relevant outcome parameters. In this chapter, we provide protocols for models of metastasis that can be used in translational and drug discovery studies.

摘要

根据定义,动物模型仅提供临床实际情况的近似值。例如,造成这种情况的一个原因是,尽管转移是肿瘤形成导致死亡的主要原因,但在药物发现和开发过程中很少将其视为靶点。由于转移对临床疾病的影响,我们认为在药物发现中除了更传统的生物学概念(包括药物药理学和毒性)外,还应考虑转移因素。药物发现和开发研究可以纳入原位和自发转移模型(同基因和异种基因)及其固有的宿主 - 肿瘤微环境相互作用,此外还可以采用确证性的原发和/或基因工程模型(GEMs)。这需要一种合理且分层的方法,使用转移性疾病模型,最好利用切除的原位原发性肿瘤和临床相关的结果参数。在本章中,我们提供了可用于转化和药物发现研究的转移模型方案。

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