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Longitudinal assessment of tumor development using cancer avatars derived from genetically engineered pluripotent stem cells.

Authors :
Koga, Tomoyuki
Koga, Tomoyuki
Chaim, Isaac A
Benitez, Jorge A
Markmiller, Sebastian
Parisian, Alison D
Hevner, Robert F
Turner, Kristen M
Hessenauer, Florian M
D'Antonio, Matteo
Nguyen, Nam-Phuong D
Saberi, Shahram
Ma, Jianhui
Miki, Shunichiro
Boyer, Antonia D
Ravits, John
Frazer, Kelly A
Bafna, Vineet
Chen, Clark C
Mischel, Paul S
Yeo, Gene W
Furnari, Frank B
Koga, Tomoyuki
Koga, Tomoyuki
Chaim, Isaac A
Benitez, Jorge A
Markmiller, Sebastian
Parisian, Alison D
Hevner, Robert F
Turner, Kristen M
Hessenauer, Florian M
D'Antonio, Matteo
Nguyen, Nam-Phuong D
Saberi, Shahram
Ma, Jianhui
Miki, Shunichiro
Boyer, Antonia D
Ravits, John
Frazer, Kelly A
Bafna, Vineet
Chen, Clark C
Mischel, Paul S
Yeo, Gene W
Furnari, Frank B
Source :
Nature communications; vol 11, iss 1, 550; 2041-1723
Publication Year :
2020

Abstract

Many cellular models aimed at elucidating cancer biology do not recapitulate pathobiology including tumor heterogeneity, an inherent feature of cancer that underlies treatment resistance. Here we introduce a cancer modeling paradigm using genetically engineered human pluripotent stem cells (hiPSCs) that captures authentic cancer pathobiology. Orthotopic engraftment of the neural progenitor cells derived from hiPSCs that have been genome-edited to contain tumor-associated genetic driver mutations revealed by The Cancer Genome Atlas project for glioblastoma (GBM) results in formation of high-grade gliomas. Similar to patient-derived GBM, these models harbor inter-tumor heterogeneity resembling different GBM molecular subtypes, intra-tumor heterogeneity, and extrachromosomal DNA amplification. Re-engraftment of these primary tumor neurospheres generates secondary tumors with features characteristic of patient samples and present mutation-dependent patterns of tumor evolution. These cancer avatar models provide a platform for comprehensive longitudinal assessment of human tumor development as governed by molecular subtype mutations and lineage-restricted differentiation.

Details

Database :
OAIster
Journal :
Nature communications; vol 11, iss 1, 550; 2041-1723
Notes :
application/pdf, Nature communications vol 11, iss 1, 550 2041-1723
Publication Type :
Electronic Resource
Accession number :
edsoai.on1287294368
Document Type :
Electronic Resource