Brief Report: External Beam Radiation Therapy for the Treatment of Human Pluripotent Stem Cell-Derived Teratomas

Author:

Lee Andrew S.1234,Tang Chad156,Hong Wan Xing134,Park Sujin1234,Bazalova-Carter Magdalena257,Nelson Geoff258,Sanchez-Freire Veronica1234,Bakerman Isaac134,Zhang Wendy234,Neofytou Evgenios1234,Connolly Andrew J.9,Chan Charles K.1,Graves Edward E.25,Weissman Irving L.1510,Nguyen Patricia K.34,Wu Joseph C.1234ORCID

Affiliation:

1. a Institute of Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California, USA

2. b Department of Radiology, Molecular Imaging Program, Stanford University School of Medicine, Stanford, California, USA

3. c Stanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, California, USA

4. d Department of Medicine, Division of Cardiology, Stanford University School of Medicine, Stanford, California, USA

5. e Department of Radiation Oncology, Stanford University School of Medicine, Stanford, California, USA

6. f Department of Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA

7. g Department of Physics and Astronomy, University of Victoria, Houston, Victoria, British Columbia, Canada

8. h Department of Radiation Oncology, University of Utah, Salt Lake City, Utah, USA

9. i Department of Pathology, Stanford University School of Medicine, Stanford, California, USA

10. j Stanford Ludwig Center for Cancer Stem Cell Research and Medicine

Abstract

Abstract Human pluripotent stem cells, including human embryonic stem cells (hESCs) and human induced PSCs (hiPSCs), have great potential as an unlimited donor source for cell-based therapeutics. The risk of teratoma formation from residual undifferentiated cells, however, remains a critical barrier to the clinical application of these cells. Herein, we describe external beam radiation therapy (EBRT) as an attractive option for the treatment of this iatrogenic growth. We present evidence that EBRT is effective in arresting growth of hESC-derived teratomas in vivo at day 28 post-implantation by using a microCT irradiator capable of targeted treatment in small animals. Within several days of irradiation, teratomas derived from injection of undifferentiated hESCs and hiPSCs demonstrated complete growth arrest lasting several months. In addition, EBRT reduced reseeding potential of teratoma cells during serial transplantation experiments, requiring irradiated teratomas to be seeded at 1 × 103 higher doses to form new teratomas. We demonstrate that irradiation induces teratoma cell apoptosis, senescence, and growth arrest, similar to established radiobiology mechanisms. Taken together, these results provide proof of concept for the use of EBRT in the treatment of existing teratomas and highlight a strategy to increase the safety of stem cell-based therapies.

Funder

National Institutes of Health

California Institute of Regenerative Medicine

Fondation Leducq Grant

American Heart Association

Burroughs Welcome Foundation

Howard Hughes Medical Institute

Stanford Cardiovascular Institute

Stanford Ludwig Center

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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