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Restricting epigenetic activity promotes the reprogramming of transformed cells to pluripotency in a line-specific manner
Somatic cell reprogramming and oncogenic transformation share surprisingly similar features, yet transformed cells are resistant to reprogramming. Epigenetic barriers must block transformed cells from reprogramming, but the nature of those barriers is unclear. In this study, we generated a systemati...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349098/ https://www.ncbi.nlm.nih.gov/pubmed/37452056 http://dx.doi.org/10.1038/s41420-023-01533-8 |
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author | Fu, Xiuling Zhuang, Qiang Babarinde, Isaac A. Shi, Liyang Ma, Gang Hu, Haoqing Li, Yuhao Chen, Jiao Xiao, Zhen Deng, Boping Sun, Li Jauch, Ralf Hutchins, Andrew P. |
author_facet | Fu, Xiuling Zhuang, Qiang Babarinde, Isaac A. Shi, Liyang Ma, Gang Hu, Haoqing Li, Yuhao Chen, Jiao Xiao, Zhen Deng, Boping Sun, Li Jauch, Ralf Hutchins, Andrew P. |
author_sort | Fu, Xiuling |
collection | PubMed |
description | Somatic cell reprogramming and oncogenic transformation share surprisingly similar features, yet transformed cells are resistant to reprogramming. Epigenetic barriers must block transformed cells from reprogramming, but the nature of those barriers is unclear. In this study, we generated a systematic panel of transformed mouse embryonic fibroblasts (MEFs) using oncogenic transgenes and discovered transformed cell lines compatible with reprogramming when transfected with Oct4/Sox2/Klf4/Myc. By comparing the reprogramming-capable and incapable transformed lines we identified multiple stages of failure in the reprogramming process. Some transformed lines failed at an early stage, whilst other lines seemed to progress through a conventional reprogramming process. Finally, we show that MEK inhibition overcomes one critical reprogramming barrier by indirectly suppressing a hyperacetylated active epigenetic state. This study reveals that diverse epigenetic barriers underly resistance to reprogramming of transformed cells. |
format | Online Article Text |
id | pubmed-10349098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103490982023-07-16 Restricting epigenetic activity promotes the reprogramming of transformed cells to pluripotency in a line-specific manner Fu, Xiuling Zhuang, Qiang Babarinde, Isaac A. Shi, Liyang Ma, Gang Hu, Haoqing Li, Yuhao Chen, Jiao Xiao, Zhen Deng, Boping Sun, Li Jauch, Ralf Hutchins, Andrew P. Cell Death Discov Article Somatic cell reprogramming and oncogenic transformation share surprisingly similar features, yet transformed cells are resistant to reprogramming. Epigenetic barriers must block transformed cells from reprogramming, but the nature of those barriers is unclear. In this study, we generated a systematic panel of transformed mouse embryonic fibroblasts (MEFs) using oncogenic transgenes and discovered transformed cell lines compatible with reprogramming when transfected with Oct4/Sox2/Klf4/Myc. By comparing the reprogramming-capable and incapable transformed lines we identified multiple stages of failure in the reprogramming process. Some transformed lines failed at an early stage, whilst other lines seemed to progress through a conventional reprogramming process. Finally, we show that MEK inhibition overcomes one critical reprogramming barrier by indirectly suppressing a hyperacetylated active epigenetic state. This study reveals that diverse epigenetic barriers underly resistance to reprogramming of transformed cells. Nature Publishing Group UK 2023-07-14 /pmc/articles/PMC10349098/ /pubmed/37452056 http://dx.doi.org/10.1038/s41420-023-01533-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Fu, Xiuling Zhuang, Qiang Babarinde, Isaac A. Shi, Liyang Ma, Gang Hu, Haoqing Li, Yuhao Chen, Jiao Xiao, Zhen Deng, Boping Sun, Li Jauch, Ralf Hutchins, Andrew P. Restricting epigenetic activity promotes the reprogramming of transformed cells to pluripotency in a line-specific manner |
title | Restricting epigenetic activity promotes the reprogramming of transformed cells to pluripotency in a line-specific manner |
title_full | Restricting epigenetic activity promotes the reprogramming of transformed cells to pluripotency in a line-specific manner |
title_fullStr | Restricting epigenetic activity promotes the reprogramming of transformed cells to pluripotency in a line-specific manner |
title_full_unstemmed | Restricting epigenetic activity promotes the reprogramming of transformed cells to pluripotency in a line-specific manner |
title_short | Restricting epigenetic activity promotes the reprogramming of transformed cells to pluripotency in a line-specific manner |
title_sort | restricting epigenetic activity promotes the reprogramming of transformed cells to pluripotency in a line-specific manner |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349098/ https://www.ncbi.nlm.nih.gov/pubmed/37452056 http://dx.doi.org/10.1038/s41420-023-01533-8 |
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