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An EWS-FLI1-Induced Osteosarcoma Model Unveiled a Crucial Role of Impaired Osteogenic Differentiation on Osteosarcoma Development

EWS-FLI1, a multi-functional fusion oncogene, is exclusively detected in Ewing sarcomas. However, previous studies reported that rare varieties of osteosarcomas also harbor EWS-ETS family fusion. Here, using the doxycycline-inducible EWS-FLI1 system, we established an EWS-FLI1-dependent osteosarcoma...

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Autores principales: Komura, Shingo, Semi, Katsunori, Itakura, Fumiaki, Shibata, Hirofumi, Ohno, Takatoshi, Hotta, Akitsu, Woltjen, Knut, Yamamoto, Takuya, Akiyama, Haruhiko, Yamada, Yasuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4834047/
https://www.ncbi.nlm.nih.gov/pubmed/26997645
http://dx.doi.org/10.1016/j.stemcr.2016.02.009
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author Komura, Shingo
Semi, Katsunori
Itakura, Fumiaki
Shibata, Hirofumi
Ohno, Takatoshi
Hotta, Akitsu
Woltjen, Knut
Yamamoto, Takuya
Akiyama, Haruhiko
Yamada, Yasuhiro
author_facet Komura, Shingo
Semi, Katsunori
Itakura, Fumiaki
Shibata, Hirofumi
Ohno, Takatoshi
Hotta, Akitsu
Woltjen, Knut
Yamamoto, Takuya
Akiyama, Haruhiko
Yamada, Yasuhiro
author_sort Komura, Shingo
collection PubMed
description EWS-FLI1, a multi-functional fusion oncogene, is exclusively detected in Ewing sarcomas. However, previous studies reported that rare varieties of osteosarcomas also harbor EWS-ETS family fusion. Here, using the doxycycline-inducible EWS-FLI1 system, we established an EWS-FLI1-dependent osteosarcoma model from murine bone marrow stromal cells. We revealed that the withdrawal of EWS-FLI1 expression enhances the osteogenic differentiation of sarcoma cells, leading to mature bone formation. Taking advantage of induced pluripotent stem cell (iPSC) technology, we also show that sarcoma-derived iPSCs with cancer-related genetic abnormalities exhibited an impaired differentiation program of osteogenic lineage irrespective of the EWS-FLI1 expression. Finally, we demonstrate that EWS-FLI1 contributed to secondary sarcoma development from the sarcoma iPSCs after osteogenic differentiation. These findings demonstrate that modulating cellular differentiation is a fundamental principle of EWS-FLI1-induced osteosarcoma development. This in vitro cancer model using sarcoma iPSCs should provide a unique platform for dissecting relationships between the cancer genome and cellular differentiation.
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spelling pubmed-48340472016-04-27 An EWS-FLI1-Induced Osteosarcoma Model Unveiled a Crucial Role of Impaired Osteogenic Differentiation on Osteosarcoma Development Komura, Shingo Semi, Katsunori Itakura, Fumiaki Shibata, Hirofumi Ohno, Takatoshi Hotta, Akitsu Woltjen, Knut Yamamoto, Takuya Akiyama, Haruhiko Yamada, Yasuhiro Stem Cell Reports Article EWS-FLI1, a multi-functional fusion oncogene, is exclusively detected in Ewing sarcomas. However, previous studies reported that rare varieties of osteosarcomas also harbor EWS-ETS family fusion. Here, using the doxycycline-inducible EWS-FLI1 system, we established an EWS-FLI1-dependent osteosarcoma model from murine bone marrow stromal cells. We revealed that the withdrawal of EWS-FLI1 expression enhances the osteogenic differentiation of sarcoma cells, leading to mature bone formation. Taking advantage of induced pluripotent stem cell (iPSC) technology, we also show that sarcoma-derived iPSCs with cancer-related genetic abnormalities exhibited an impaired differentiation program of osteogenic lineage irrespective of the EWS-FLI1 expression. Finally, we demonstrate that EWS-FLI1 contributed to secondary sarcoma development from the sarcoma iPSCs after osteogenic differentiation. These findings demonstrate that modulating cellular differentiation is a fundamental principle of EWS-FLI1-induced osteosarcoma development. This in vitro cancer model using sarcoma iPSCs should provide a unique platform for dissecting relationships between the cancer genome and cellular differentiation. Elsevier 2016-03-17 /pmc/articles/PMC4834047/ /pubmed/26997645 http://dx.doi.org/10.1016/j.stemcr.2016.02.009 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Komura, Shingo
Semi, Katsunori
Itakura, Fumiaki
Shibata, Hirofumi
Ohno, Takatoshi
Hotta, Akitsu
Woltjen, Knut
Yamamoto, Takuya
Akiyama, Haruhiko
Yamada, Yasuhiro
An EWS-FLI1-Induced Osteosarcoma Model Unveiled a Crucial Role of Impaired Osteogenic Differentiation on Osteosarcoma Development
title An EWS-FLI1-Induced Osteosarcoma Model Unveiled a Crucial Role of Impaired Osteogenic Differentiation on Osteosarcoma Development
title_full An EWS-FLI1-Induced Osteosarcoma Model Unveiled a Crucial Role of Impaired Osteogenic Differentiation on Osteosarcoma Development
title_fullStr An EWS-FLI1-Induced Osteosarcoma Model Unveiled a Crucial Role of Impaired Osteogenic Differentiation on Osteosarcoma Development
title_full_unstemmed An EWS-FLI1-Induced Osteosarcoma Model Unveiled a Crucial Role of Impaired Osteogenic Differentiation on Osteosarcoma Development
title_short An EWS-FLI1-Induced Osteosarcoma Model Unveiled a Crucial Role of Impaired Osteogenic Differentiation on Osteosarcoma Development
title_sort ews-fli1-induced osteosarcoma model unveiled a crucial role of impaired osteogenic differentiation on osteosarcoma development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4834047/
https://www.ncbi.nlm.nih.gov/pubmed/26997645
http://dx.doi.org/10.1016/j.stemcr.2016.02.009
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