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Modeling Patient-Derived Glioblastoma with Cerebral Organoids
Author(s) -
Amanda Linkous,
Demosthenes Balamatsias,
Matija Snuderl,
Lincoln Edwards,
Ken Miyaguchi,
Teresa A. Milner,
Batsheva Reich,
Leona CohenGould,
Andrew J. Storaska,
Yasumi Nakayama,
Emily Schenkein,
Richa Singhania,
Stéfano M. Cirigliano,
Tarig Magdeldin,
Ying Lin,
Gouri J. Nanjangud,
Kalyani Chadalavada,
David J. Pisapia,
Conor Liston,
Howard A. Fine
Publication year - 2019
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2019.02.063
Subject(s) - organoid , embryonic stem cell , glioblastoma , phenocopy , glioma , human brain , ex vivo , stem cell , biology , cancer research , in vivo , neuroscience , pathology , medicine , phenotype , microbiology and biotechnology , gene , genetics
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.

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