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Correlation Between Genetic Abnormalities in Induced Pluripotent Stem Cell-Derivatives and Abnormal Tissue Formation in Tumorigenicity Tests
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 abnorm...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9154342/ https://www.ncbi.nlm.nih.gov/pubmed/35445254 http://dx.doi.org/10.1093/stcltm/szac014 |
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author | Yamamoto, Takako Sato, Yoji Yasuda, Satoshi Shikamura, Masayuki Tamura, Takashi Takenaka, Chiemi Takasu, Naoko Nomura, Masaki Dohi, Hiromi Takahashi, Masayo Mandai, Michiko Kanemura, Yonehiro Nakamura, Masaya Okano, Hideyuki Kawamata, Shin |
author_facet | Yamamoto, Takako Sato, Yoji Yasuda, Satoshi Shikamura, Masayuki Tamura, Takashi Takenaka, Chiemi Takasu, Naoko Nomura, Masaki Dohi, Hiromi Takahashi, Masayo Mandai, Michiko Kanemura, Yonehiro Nakamura, Masaya Okano, Hideyuki Kawamata, Shin |
author_sort | Yamamoto, Takako |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9154342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-91543422022-06-04 Correlation Between Genetic Abnormalities in Induced Pluripotent Stem Cell-Derivatives and Abnormal Tissue Formation in Tumorigenicity Tests Yamamoto, Takako Sato, Yoji Yasuda, Satoshi Shikamura, Masayuki Tamura, Takashi Takenaka, Chiemi Takasu, Naoko Nomura, Masaki Dohi, Hiromi Takahashi, Masayo Mandai, Michiko Kanemura, Yonehiro Nakamura, Masaya Okano, Hideyuki Kawamata, Shin Stem Cells Transl Med Pluripotent Stem Cells 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. Oxford University Press 2022-04-21 /pmc/articles/PMC9154342/ /pubmed/35445254 http://dx.doi.org/10.1093/stcltm/szac014 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Pluripotent Stem Cells Yamamoto, Takako Sato, Yoji Yasuda, Satoshi Shikamura, Masayuki Tamura, Takashi Takenaka, Chiemi Takasu, Naoko Nomura, Masaki Dohi, Hiromi Takahashi, Masayo Mandai, Michiko Kanemura, Yonehiro Nakamura, Masaya Okano, Hideyuki Kawamata, Shin Correlation Between Genetic Abnormalities in Induced Pluripotent Stem Cell-Derivatives and Abnormal Tissue Formation in Tumorigenicity Tests |
title | Correlation Between Genetic Abnormalities in Induced Pluripotent Stem Cell-Derivatives and Abnormal Tissue Formation in Tumorigenicity Tests |
title_full | Correlation Between Genetic Abnormalities in Induced Pluripotent Stem Cell-Derivatives and Abnormal Tissue Formation in Tumorigenicity Tests |
title_fullStr | Correlation Between Genetic Abnormalities in Induced Pluripotent Stem Cell-Derivatives and Abnormal Tissue Formation in Tumorigenicity Tests |
title_full_unstemmed | Correlation Between Genetic Abnormalities in Induced Pluripotent Stem Cell-Derivatives and Abnormal Tissue Formation in Tumorigenicity Tests |
title_short | Correlation Between Genetic Abnormalities in Induced Pluripotent Stem Cell-Derivatives and Abnormal Tissue Formation in Tumorigenicity Tests |
title_sort | correlation between genetic abnormalities in induced pluripotent stem cell-derivatives and abnormal tissue formation in tumorigenicity tests |
topic | Pluripotent Stem Cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9154342/ https://www.ncbi.nlm.nih.gov/pubmed/35445254 http://dx.doi.org/10.1093/stcltm/szac014 |
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