| Literature DB >> 26826297 |
Francesca Del Bufalo1, Teresa Manzo2, Valentina Hoyos2, Shigeki Yagyu2, Ignazio Caruana3, Jeffrey Jacot4, Omar Benavides5, Daniel Rosen6, Malcolm K Brenner2.
Abstract
Interactions between malignant and stromal cells and the 3D spatial architecture of the tumor both substantially modify tumor behavior, including the responses to small molecule drugs and biological therapies. Conventional 2D culture systems cannot replicate this complexity. To overcome these limitations and more accurately model solid tumors, we developed a highly versatile 3D PEG-fibrin hydrogel model of human lung adenocarcinoma. Our model relevantly recapitulates the effect of oncolytic adenovirus; tumor responses in this setting nearly reproduce those observed in vivo. We have also validated the use of this model for complex, long-term, 3D cultures of cancer cells and their stroma (fibroblasts and endothelial cells). Both tumor proliferation and invasiveness were enhanced in the presence of stromal components. These results validate our 3D hydrogel model as a relevant platform to study cancer biology and tumor responses to biological treatments.Entities:
Keywords: 3D tumor model; Oncolytic adenovirus; Preclinical drug testing; Tumor microenvironment
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Year: 2016 PMID: 26826297 DOI: 10.1016/j.biomaterials.2016.01.030
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479