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临床前癌症研究中的原位和转移瘤模型。

Orthotopic and metastatic tumour models in preclinical cancer research.

作者信息

Stribbling Stephen M, Beach Callum, Ryan Anderson J

机构信息

Department of Chemistry, University College London, Gower Street, London WC1E 6BT, UK.

Department of Oncology, University of Oxford, ORCRB, Roosevelt Drive, Oxford OX3 7DQ, UK.

出版信息

Pharmacol Ther. 2024 May;257:108631. doi: 10.1016/j.pharmthera.2024.108631. Epub 2024 Mar 11.

Abstract

Mouse models of disease play a pivotal role at all stages of cancer drug development. Cell-line derived subcutaneous tumour models are predominant in early drug discovery, but there is growing recognition of the importance of the more complex orthotopic and metastatic tumour models for understanding both target biology in the correct tissue context, and the impact of the tumour microenvironment and the immune system in responses to treatment. The aim of this review is to highlight the value that orthotopic and metastatic models bring to the study of tumour biology and drug development while pointing out those models that are most likely to be encountered in the literature. Important developments in orthotopic models, such as the increasing use of early passage patient material (PDXs, organoids) and humanised mouse models are discussed, as these approaches have the potential to increase the predictive value of preclinical studies, and ultimately improve the success rate of anticancer drugs in clinical trials.

摘要

疾病小鼠模型在癌症药物研发的各个阶段都起着关键作用。细胞系衍生的皮下肿瘤模型在早期药物发现中占主导地位,但人们越来越认识到,更复杂的原位和转移肿瘤模型对于在正确的组织背景下理解靶标生物学,以及肿瘤微环境和免疫系统对治疗反应的影响至关重要。本综述的目的是强调原位和转移模型为肿瘤生物学研究和药物研发带来的价值,同时指出文献中最可能遇到的那些模型。文中讨论了原位模型的重要进展,如早期传代患者材料(PDXs、类器官)和人源化小鼠模型的使用增加,因为这些方法有可能提高临床前研究的预测价值,并最终提高抗癌药物在临床试验中的成功率。

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