Modeling Human Brain Tumors and the Microenvironment Using Induced Pluripotent Stem Cells.
Zahraa I KhamisDrishty B SarkerYu XueNancy Al-AkkaryViviana D JamesChangchun ZengYan LiQing-Xiang Amy SangPublished in: Cancers (2023)
Brain cancer is a group of diverse and rapidly growing malignancies that originate in the central nervous system (CNS) and have a poor prognosis. The complexity of brain structure and function makes brain cancer modeling extremely difficult, limiting pathological studies and therapeutic developments. Advancements in human pluripotent stem cell technology have opened a window of opportunity for brain cancer modeling, providing a wealth of customizable methods to simulate the disease in vitro. This is achieved with the advent of genome editing and genetic engineering technologies that can simulate germline and somatic mutations found in human brain tumors. This review investigates induced pluripotent stem cell (iPSC)-based approaches to model human brain cancer. The applications of iPSCs as renewable sources of individual brain cell types, brain organoids, blood-brain barrier (BBB), and brain tumor models are discussed. The brain tumor models reviewed are glioblastoma and medulloblastoma. The iPSC-derived isogenic cells and three-dimensional (3D) brain cancer organoids combined with patient-derived xenografts will enhance future compound screening and drug development for these deadly human brain cancers.
Keyphrases
- induced pluripotent stem cells
- papillary thyroid
- blood brain barrier
- stem cells
- resting state
- white matter
- poor prognosis
- cerebral ischemia
- endothelial cells
- squamous cell
- functional connectivity
- lymph node metastasis
- multiple sclerosis
- long non coding rna
- oxidative stress
- squamous cell carcinoma
- gene expression
- mesenchymal stem cells
- signaling pathway
- copy number
- bone marrow
- brain injury
- genome wide
- drug induced
- cerebrospinal fluid
- diabetic rats
- current status
- high glucose