胰腺癌
癌症研究
信号转导
烧蚀
癌症
医学
生物信息学
计算生物学
生物
细胞生物学
内科学
作者
Duc-Huy T. Nguyen,Esak Lee,Styliani Alimperti,Robert J. Norgard,Alec Wong,Jake June-Koo Lee,Jeroen Eyckmans,Ben Z. Stanger,Christopher S. Chen
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2019-08-02
卷期号:5 (8)
被引量:150
标识
DOI:10.1126/sciadv.aav6789
摘要
Pancreatic ductal adenocarcinoma (PDAC) is an aggressive, lethal malignancy that invades adjacent vasculatures and spreads to distant sites before clinical detection. Although invasion into the peripancreatic vasculature is one of the hallmarks of PDAC, paradoxically, PDAC tumors also exhibit hypovascularity. How PDAC tumors become hypovascular is poorly understood. We describe an organotypic PDAC-on-a-chip culture model that emulates vascular invasion and tumor-blood vessel interactions to better understand PDAC-vascular interactions. The model features a 3D matrix containing juxtaposed PDAC and perfusable endothelial lumens. PDAC cells invaded through intervening matrix, into vessel lumen, and ablated the endothelial cells, leaving behind tumor-filled luminal structures. Endothelial ablation was also observed in in vivo PDAC models. We also identified the activin-ALK7 pathway as a mediator of endothelial ablation by PDAC. This tumor-on-a-chip model provides an important in vitro platform for investigating the process of PDAC-driven endothelial ablation and may provide a mechanism for tumor hypovascularity.
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