TY - JOUR
T1 - Stem cell modeling of nervous system tumors
AU - Furnari, Frank B.
AU - Anastasaki, Corina
AU - Bian, Shan
AU - Fine, Howard A.
AU - Koga, Tomoyuki
AU - Le, Lu Q.
AU - Rodriguez, Fausto J.
AU - Gutmann, David H.
N1 - Publisher Copyright:
© 2024 Company of Biologists Ltd. All rights reserved.
PY - 2024/2
Y1 - 2024/2
N2 - Nervous system tumors, particularly brain tumors, represent the most common tumors in children and one of the most lethal tumors in adults. Despite decades of research, there are few effective therapies for these cancers. Although human nervous system tumor cells and genetically engineered mouse models have served as excellent platforms for drug discovery and preclinical testing, they have limitations with respect to accurately recapitulating important aspects of the pathobiology of spontaneously arising human tumors. For this reason, attention has turned to the deployment of human stem cell engineering involving human embryonic or induced pluripotent stem cells, in which genetic alterations associated with nervous system cancers can be introduced. These stem cells can be used to create self-assembling three-dimensional cerebral organoids that preserve key features of the developing human brain. Moreover, stem cell-engineered lines are amenable to xenotransplantation into mice as a platform to investigate the tumor cell of origin, discover cancer evolutionary trajectories and identify therapeutic vulnerabilities. In this article, we review the current state of human stem cell models of nervous system tumors, discuss their advantages and disadvantages, and provide consensus recommendations for future research.
AB - Nervous system tumors, particularly brain tumors, represent the most common tumors in children and one of the most lethal tumors in adults. Despite decades of research, there are few effective therapies for these cancers. Although human nervous system tumor cells and genetically engineered mouse models have served as excellent platforms for drug discovery and preclinical testing, they have limitations with respect to accurately recapitulating important aspects of the pathobiology of spontaneously arising human tumors. For this reason, attention has turned to the deployment of human stem cell engineering involving human embryonic or induced pluripotent stem cells, in which genetic alterations associated with nervous system cancers can be introduced. These stem cells can be used to create self-assembling three-dimensional cerebral organoids that preserve key features of the developing human brain. Moreover, stem cell-engineered lines are amenable to xenotransplantation into mice as a platform to investigate the tumor cell of origin, discover cancer evolutionary trajectories and identify therapeutic vulnerabilities. In this article, we review the current state of human stem cell models of nervous system tumors, discuss their advantages and disadvantages, and provide consensus recommendations for future research.
KW - Brain tumor
KW - CRISPR engineering
KW - Nerve sheath tumors
KW - human embryonic stem cells (hESCs)
KW - human induced pluripotent stem cells (hiPSCs)
UR - http://www.scopus.com/inward/record.url?scp=85185208356&partnerID=8YFLogxK
U2 - 10.1242/dmm.050533
DO - 10.1242/dmm.050533
M3 - Article
C2 - 38353122
AN - SCOPUS:85185208356
SN - 1754-8403
VL - 17
SP - 1
EP - 13
JO - DMM Disease Models and Mechanisms
JF - DMM Disease Models and Mechanisms
IS - 2
M1 - dmm050533
ER -