Miquel Maria, Zhang Shuman, Pilarsky Christian
Department of Surgery, University Hospital, Erlangen, Germany.
Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Front Cell Dev Biol. 2021 Oct 27;9:748631. doi: 10.3389/fcell.2021.748631. eCollection 2021.
Pancreatic ductal adenocarcinoma (PDAC) is a hostile solid malignancy coupled with an extremely high mortality rate. Metastatic disease is already found in most patients at the time of diagnosis, resulting in a 5-year survival rate below 5%. Improved comprehension of the mechanisms leading to metastasis is pivotal for the development of new targeted therapies. A key field to be improved are modeling strategies applied in assessing cancer progression, since traditional platforms fail in recapitulating the complexity of PDAC. Consequently, there is a compelling demand for new preclinical models that mirror tumor progression incorporating the pressure of the immune system, tumor microenvironment, as well as molecular aspects of PDAC. We suggest the incorporation of 3D organoids derived from genetically engineered mouse models or patients as promising new tools capable to transform PDAC pre-clinical modeling and access new frontiers in personalized medicine.
胰腺导管腺癌(PDAC)是一种恶性实体肿瘤,死亡率极高。大多数患者在诊断时就已出现转移性疾病,导致5年生存率低于5%。深入了解导致转移的机制对于开发新的靶向治疗至关重要。一个需要改进的关键领域是用于评估癌症进展的建模策略,因为传统平台无法重现PDAC的复杂性。因此,迫切需要新的临床前模型来反映肿瘤进展,同时纳入免疫系统压力、肿瘤微环境以及PDAC的分子特征。我们建议将源自基因工程小鼠模型或患者的3D类器官作为有前景的新工具,能够改变PDAC临床前建模并开启个性化医学的新前沿。