临床前嗜铬细胞瘤和副神经节瘤模型:细胞系、动物模型和人类原代培养模型。

Katharina Wang, Alessa Fischer, Umberto Maccio, Constanze Hantel, Felix Beuschlein, Ashley B Grossman, Karel Pacak, Svenja Nölting
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引用次数: 0

摘要

几十年的研究证明,建立人类嗜铬细胞瘤和副神经节瘤(PPGL)细胞系特别困难,但目前还有其他可靠的临床前 PPGL 模型可用。本综述概述了这些模型,以及我们最近利用源自患者的 PPGL 原始培养物建立的个性化药物筛选平台。目前可用的 PPGL 模型包括小鼠和大鼠 PPGL 细胞系(其中只有一种细胞系(PC12)可通过细胞储存库公开获取)和 PPGL 动物模型(其中患者来源的异种移植模型很有前景,但建立起来很复杂)。我们已开发出人类 PPGL 原始培养物的下一代实施方案,可根据肿瘤独特的遗传、生化、免疫组化和临床特征进行可靠的个性化药物筛选和肿瘤药物反应性的个体化分析。总之,可靠的 PPGL 模型(包括源自患者的原代培养模型)对于推进 PPGL 领域的临床前研究至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pre-clinical phaeochromocytoma and paraganglioma models: Cell lines, animal models, and a human primary culture model.

While the establishment of human phaeochromocytoma and paraganglioma (PPGL) cell lines has proven to be particularly difficult over several decades of research, there are other reliable pre-clinical PPGL models currently available. This review provides a summary of these models, together with our recently established personalised drug screening platform using patient-derived PPGL primary cultures. Such currently available PPGL models include murine and rat PPGL cell lines, of which only one cell line (PC12) is publicly accessible through a cell repository, and PPGL animal models, of which the patient-derived xenograft models are promising but complex to establish. We have developed next-generation implementation of human PPGL primary cultures, enabling reliable and personalised drug screening and an individualised analysis of tumour drug responsivity based on the tumour's unique genetic, biochemical, immunohistochemical and clinical profile. Overall, reliable PPGL models, including patient-derived primary culture models, are essential to advance pre-clinical research in the field of PPGLs.

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