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Patient-Derived Xenografts of Non Small Cell Lung Cancer: Resurgence of an Old Model for Investigation of Modern Concepts of Tailored Therapy and Cancer Stem Cells

机译:非小细胞肺癌患者来源的异种移植:一种旧模型的复活研究现代的定制疗法和癌症干细胞的概念。

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摘要

Current chemotherapy regimens have unsatisfactory results in most advanced solid tumors. It is therefore imperative to devise novel therapeutic strategies and to optimize selection of patients, identifying early those who could benefit from available treatments. Mouse models are the most valuable tool for preclinical evaluation of novel therapeutic strategies in cancer and, among them, patient-derived xenografts models (PDX) have made a recent comeback in popularity. These models, obtained by direct implants of tissue fragments in immunocompromised mice, have great potential in drug development studies because they faithfully reproduce the patient's original tumor for both immunohistochemical markers and genetic alterations as well as in terms of response to common therapeutics They also maintain the original tumor heterogeneity, allowing studies of specific cellular subpopulations, including their modulation after drug treatment. Moreover PDXs maintain at least some aspects of the human microenvironment for weeks with the complete substitution with murine stroma occurring only after 2-3 passages in mouse and represent therefore a promising model for studies of tumor-microenvironment interaction. This review summarizes our present knowledge on mouse preclinical cancer models, with a particular attention on patient-derived xenografts of non small cell lung cancer and their relevance for preclinical and biological studies.
机译:当前的化疗方案在大多数晚期实体瘤中均不能令人满意。因此,必须设计出新颖的治疗策略并优化患者选择,尽早确定可从现有治疗中受益的患者。小鼠模型是用于临床前评估癌症新治疗策略的最有价值的工具,其中,患者衍生的异种移植模型(PDX)近期流行起来。这些模型是通过将组织片段直接植入免疫受损的小鼠体内而获得的,在药物开发研究中具有巨大潜力,因为它们忠实地再现了患者的原始肿瘤的免疫组织化学标记和遗传改变,以及对常见疗法的反应。原始的肿瘤异质性,可以研究特定的细胞亚群,包括药物治疗后的亚群。此外,PDX至少在人类微环境的某些方面维持了数周,而仅在小鼠2-3次传代后才发生鼠基质的完全替代,因此代表了一种有希望的模型,用于研究肿瘤微环境的相互作用。这篇综述总结了我们目前关于小鼠临床前癌症模型的知识,特别关注了患者来源的非小细胞肺癌异种移植及其与临床前和生物学研究的相关性。

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