| Literature DB >> 30893594 |
Amanda Linkous1, Demosthenes Balamatsias1, Matija Snuderl2, Lincoln Edwards1, Ken Miyaguchi1, Teresa Milner3, Batsheva Reich3, Leona Cohen-Gould4, Andrew Storaska1, Yasumi Nakayama1, Emily Schenkein1, Richa Singhania1, Stefano Cirigliano1, Tarig Magdeldin1, Ying Lin1, Gouri Nanjangud5, Kalyani Chadalavada5, David Pisapia6, Conor Liston3, Howard A Fine7.
Abstract
The prognosis of patients with glioblastoma (GBM) remains dismal, with a median survival of approximately 15 months. Current preclinical GBM models are limited by the lack of a "normal" human microenvironment and the inability of many tumor cell lines to accurately reproduce GBM biology. To address these limitations, we have established a model system whereby we can retro-engineer patient-specific GBMs using patient-derived glioma stem cells (GSCs) and human embryonic stem cell (hESC)-derived cerebral organoids. Our cerebral organoid glioma (GLICO) model shows that GSCs home toward the human cerebral organoid and deeply invade and proliferate within the host tissue, forming tumors that closely phenocopy patient GBMs. Furthermore, cerebral organoid tumors form rapidly and are supported by an interconnected network of tumor microtubes that aids in the invasion of normal host tissue. Our GLICO model provides a system for modeling primary human GBM ex vivo and for high-throughput drug screening.Entities:
Keywords: brain tumors; cancer stem cells; cerebral organoids; glioblastoma; glioma; glioma stem cells; human embryonic stem cells; stem-cell-based disease models; tissue engineering; tumor microtubes
Mesh:
Year: 2019 PMID: 30893594 PMCID: PMC6625753 DOI: 10.1016/j.celrep.2019.02.063
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423