| Literature DB >> 30265900 |
Xuanyi Ma1, Claire Yu2, Pengrui Wang3, Weizhe Xu1, Xueyi Wan4, Cheuk Sun Edwin Lai5, Justin Liu3, Anna Koroleva-Maharajh2, Shaochen Chen6.
Abstract
Hepatocellular carcinoma (HCC), as the fifth most common malignant cancer, develops and progresses mostly in a cirrhotic liver where stiff nodules are separated by fibrous bands. Scaffolds that can provide a 3D cirrhotic mechanical environment with complex native composition and biomimetic architecture are necessary for the development of better predictive tissue models. Here, we developed photocrosslinkable liver decellularized extracellular matrix (dECM) and a rapid light-based 3D bioprinting process to pattern liver dECM with tailorable mechanical properties to serve as a platform for HCC progression study. 3D bioprinted liver dECM scaffolds were able to stably recapitulate the clinically relevant mechanical properties of cirrhotic liver tissue. When encapsulated in dECM scaffolds with cirrhotic stiffness, HepG2 cells demonstrated reduced growth along with an upregulation of invasion markers compared to healthy controls. Moreover, an engineered cancer tissue platform possessing tissue-scale organization and distinct regional stiffness enabled the visualization of HepG2 stromal invasion from the nodule with cirrhotic stiffness. This work demonstrates a significant advancement in rapid 3D patterning of complex ECM biomaterials with biomimetic architecture and tunable mechanical properties for in vitro disease modeling.Entities:
Keywords: 3D bioprinting; Cancer invasion; Decellularized extracellular matrix; Liver fibrosis; Tissue engineering
Mesh:
Substances:
Year: 2018 PMID: 30265900 PMCID: PMC6186504 DOI: 10.1016/j.biomaterials.2018.09.026
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479