Correlation Between Genetic Abnormalities in Induced Pluripotent Stem Cell-Derivatives and Abnormal Tissue Formation in Tumorigenicity Tests

Author:

Yamamoto Takako1ORCID,Sato Yoji2ORCID,Yasuda Satoshi2,Shikamura Masayuki1,Tamura Takashi1,Takenaka Chiemi1,Takasu Naoko3,Nomura Masaki3,Dohi Hiromi3,Takahashi Masayo45,Mandai Michiko4,Kanemura Yonehiro6,Nakamura Masaya7,Okano Hideyuki8,Kawamata Shin14

Affiliation:

1. R&D Center for Cell Therapy, Foundation for Biomedical Research and Innovation , Kobe , Japan

2. Division of Cell-Based Therapeutic Products, National Institute of Health Sciences , Kawasaki , Japan

3. CiRA Foundation , Kyoto , Japan

4. Riken BDR , Kobe , Japan

5. Vison Care Inc. , Kobe , Japan

6. Department of Biomedical Research and Innovation, Institute for Clinical Research, National Hospital Organization Osaka National Hospital , Osaka , Japan

7. Department of Orthopedic Surgery, Keio University School of Medicine , Tokyo , Japan

8. Department of Physiology, Keio University School of Medicine , Tokyo , Japan

Abstract

Abstract Cell therapy using induced pluripotent stem cell (iPSC) derivatives may result in abnormal tissue generation because the cells undergo numerous cycles of mitosis before clinical application, potentially increasing the accumulation of genetic abnormalities. Therefore, genetic tests may predict abnormal tissue formation after transplantation. Here, we administered iPSC derivatives with or without single-nucleotide variants (SNVs) and deletions in cancer-related genes with various genomic copy number variant (CNV) profiles into immunodeficient mice and examined the relationships between mutations and abnormal tissue formation after transplantation. No positive correlations were found between the presence of SNVs/deletions and the formation of abnormal tissues; the overall predictivity was 29%. However, a copy number higher than 3 was correlated, with an overall predictivity of 86%. Furthermore, we found CNV hotspots at 14q32.33 and 17q12 loci. Thus, CNV analysis may predict abnormal tissue formation after transplantation of iPSC derivatives and reduce the number of tumorigenicity tests.

Funder

Japan Ministry of Health

Labour and Welfare

Japan Agency for Medical Research and Development

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,General Medicine

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