Baker Lindsey A, Tiriac Hervé, Clevers Hans, Tuveson David A
Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA; Lustgarten Pancreatic Cancer Research Laboratory, Cold Spring Harbor, NY 11724, USA.
Hubrecht Institute and University Medical Centre Utrecht, Utrecht, The Netherlands.
Trends Cancer. 2016 Apr;2(4):176-190. doi: 10.1016/j.trecan.2016.03.004.
Pancreatic ductal adenocarcinoma (PDA) is a highly lethal malignancy for which new treatment and diagnostic approaches are urgently needed. In order for such breakthroughs to be discovered, researchers require systems that accurately model the development and biology of PDA. While cell lines, genetically engineered murine models, and xenografts have all led to valuable clinical insights, organotypic culture models have emerged as tractable systems to recapitulate the complex three-dimensional organization of PDA. Recently, multiple methods for modeling PDA using organoids have been reported. This review aims to summarize these organoid methods in the context of other PDA models. While each model system has unique benefits and drawbacks, ultimately, organoids hold special promise for the development of personalized medicine approaches.
胰腺导管腺癌(PDA)是一种极具致死性的恶性肿瘤,迫切需要新的治疗和诊断方法。为了发现此类突破,研究人员需要能够准确模拟PDA发生发展及生物学特性的系统。虽然细胞系、基因工程小鼠模型和异种移植都带来了有价值的临床见解,但器官型培养模型已成为概括PDA复杂三维组织结构的易处理系统。最近,已有多种使用类器官构建PDA模型的方法被报道。本综述旨在结合其他PDA模型总结这些类器官方法。虽然每个模型系统都有独特的优缺点,但最终,类器官在个性化医疗方法的开发方面具有特殊前景。