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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
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.
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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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