软组织肉瘤发生的临床前模型及其应用,以加强转化研究。

Sandro Pasquali, David S Moura, Molly R Danks, Piotr J Manasterski, Nadia Zaffaroni, Silvia Stacchiotti, Jose L Mondaza-Hernandez, William G J Kerrison, Javier Martin-Broto, Paul H Huang, Valerie G Brunton
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引用次数: 0

摘要

软组织肉瘤(STS)是一大类罕见和超罕见的肿瘤,具有独特的形态、分子和临床特征。患有这种罕见癌症的患者通常在临床试验中代表性不足,这限制了新治疗方案的引入和随后患者预后的改善。概括人类疾病的STS临床前模型可以帮助确定新的有效治疗方法。然而,由于这些肿瘤的罕见性,可用的STS模型有限。在这里,我们回顾了现有的STS临床前模型,包括患者来源的细胞系和类器官,患者来源的异种移植和基因工程小鼠模型。我们讨论了不同模型的优点和缺点,并描述了他们在多大程度上辅助临床翻译。最后,我们考虑了未来可以做些什么来提高他们在临床前的预测能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preclinical models of soft tissue sarcomas - generation and applications to enhance translational research.

Soft tissue sarcomas (STS) represent a large group of rare and ultra-rare tumors distinguished by unique morphological, molecular and clinical features. Patients with such rare cancers are generally underrepresented in clinical trials which has limited the introduction of new treatment options and subsequent improvement of patient outcomes. Preclinical models of STS that recapitulate the human disease can aid progress in identifying new effective treatments. However, due to the rarity of these tumors there are limited STS models available. Here we review the existing preclinical models of STS, including patient-derived cell lines and organoids, patient-derived xenografts and genetically engineered mouse models. We discuss the advantages and disadvantages of the different models and describe to what extent they have aided clinical translation. Finally, we consider what can be done in the future to enhance their predictivity in the preclinical setting.

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