Modeling Human Brain Tumors and the Microenvironment Using Induced Pluripotent Stem Cells

Author:

Khamis Zahraa I.1234,Sarker Drishty B.1ORCID,Xue Yu1ORCID,Al-Akkary Nancy4,James Viviana D.1,Zeng Changchun23ORCID,Li Yan56ORCID,Sang Qing-Xiang Amy16ORCID

Affiliation:

1. Department of Chemistry and Biochemistry, Florida State University, Tallahassee, FL 32306, USA

2. Department of Industrial and Manufacturing Engineering, FAMU-FSU College of Engineering, Florida State University, Tallahassee, FL 32310, USA

3. High-Performance Materials Institute, Florida State University, Tallahassee, FL 32310, USA

4. Laboratory of Cancer Biology and Molecular Immunology, Department of Biochemistry, Faculty of Sciences-I, Lebanese University, Beirut, Lebanon

5. Department of Chemical and Biomedical Engineering, FAMU-FSU College of Engineering, Florida State University, Tallahassee, FL 32306, USA

6. Institute of Molecular Biophysics, Florida State University, Tallahassee, FL 32306, USA

Abstract

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.

Funder

Florida Department of Health

Florida State University Council

Publisher

MDPI AG

Subject

Cancer Research,Oncology

Reference138 articles.

1. Mitalipov, S., and Wolf, D. (2009). Engineering of Stem Cells, Springer.

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3. Nuclear reprogramming and pluripotency;Hochedlinger;Nature,2006

4. Induced pluripotent stem cells: Past, present, and future;Yamanaka;Cell Stem Cell,2012

5. Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors;Takahashi;Cell,2006

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