Department of Internal Medicine I, Martin-Luther University Halle/Wittenberg, Ernst-Grube-Strasse 40, D-06120 Halle (Saale), Germany.
Department of Medicine, Internal Medicine IV, University Hospital Heidelberg, Im Neuenheimer Feld 410, D-69120 Heidelberg, Germany.
Cells. 2022 Oct 10;11(19):3170. doi: 10.3390/cells11193170.
Pancreatic ductal adenocarcinoma (PDAC) is the most common pancreatic malignancy with a 5-year survival rate below 10%, thereby exhibiting the worst prognosis of all solid tumors. Increasing incidence together with a continued lack of targeted treatment options will cause PDAC to be the second leading cause of cancer-related deaths in the western world by 2030. Obesity belongs to the predominant risk factors for pancreatic cancer. To improve our understanding of the impact of obesity on pancreatic cancer development and progression, novel laboratory techniques have been developed. In this review, we summarize current in vitro and in vivo models of PDAC and obesity as well as an overview of a variety of models to investigate obesity-driven pancreatic carcinogenesis. We start by giving an overview on different methods to cultivate adipocytes in vitro as well as various in vivo mouse models of obesity. Moreover, established murine and human PDAC cell lines as well as organoids are summarized and the genetically engineered models of PCAC compared to xenograft models are introduced. Finally, we review published in vitro and in vivo models studying the impact of obesity on PDAC, enabling us to decipher the molecular basis of obesity-driven pancreatic carcinogenesis.
胰腺导管腺癌(PDAC)是最常见的胰腺恶性肿瘤,5 年生存率低于 10%,因此是所有实体瘤中预后最差的。发病率的增加加上缺乏靶向治疗选择,到 2030 年 PDAC 将成为西方世界癌症相关死亡的第二大主要原因。肥胖属于胰腺癌的主要危险因素之一。为了更好地了解肥胖对胰腺癌发展和进展的影响,开发了新的实验室技术。在这篇综述中,我们总结了当前 PDAC 和肥胖的体外和体内模型,以及各种研究肥胖驱动的胰腺癌发生的模型概述。我们首先概述了体外培养脂肪细胞的不同方法以及各种肥胖的体内小鼠模型。此外,还总结了已建立的鼠和人 PDAC 细胞系和类器官,并介绍了与异种移植模型相比的基因工程 PCAC 模型。最后,我们综述了已发表的研究肥胖对 PDAC 影响的体外和体内模型,使我们能够揭示肥胖驱动的胰腺癌发生的分子基础。