Preclinical mouse models for immunotherapeutic and non-immunotherapeutic drug development for pancreatic ductal adenocarcinoma.

Annals of Pancreatic Cancer Pub Date : 2020-07-01 Epub Date: 2020-07-22 DOI:10.21037/apc.2020.03.03
Mengni He, MacKenzie Henderson, Stephen Muth, Adrian Murphy, Lei Zheng
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引用次数: 16

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is in urgent need of better diagnostic and therapeutic methods due to its late diagnosis, limited treatment options and poor prognosis. Finding the right animal models to recapitulate the tumor molecular pathogenesis and tumor microenvironment (TME) complexity is critical for preclinical immunotherapeutic and non-immunotherapeutic treatment developments. In this review, we summarize and evaluate popular preclinical animal models including patient-derived xenograft models, humanized mouse models, genetically engineered mouse models, and syngeneic mouse models. Through comparisons between these models in different research settings, we hope to provide guidance in finding the most relevant preclinical models to suit various research purposes.

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用于胰腺导管腺癌免疫治疗和非免疫治疗药物开发的临床前小鼠模型。
胰腺导管腺癌(Pancreatic ductal adencarcinoma, PDAC)由于诊断较晚、治疗方案有限、预后较差,迫切需要更好的诊断和治疗方法。寻找合适的动物模型来概括肿瘤分子发病机制和肿瘤微环境(TME)的复杂性对于临床前免疫治疗和非免疫治疗治疗的发展至关重要。在这篇综述中,我们总结和评价了常用的临床前动物模型,包括患者来源的异种移植模型、人源化小鼠模型、基因工程小鼠模型和同基因小鼠模型。通过对这些模型在不同研究环境下的比较,我们希望为寻找最相关的临床前模型提供指导,以适应各种研究目的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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0.90
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