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Myogenic regulatory transcription factors regulate growth in rhabdomyosarcoma
Rhabdomyosarcoma (RMS) is a pediatric malignacy of muscle with myogenic regulatory transcription factors MYOD and MYF5 being expressed in this disease. Consensus in the field has been that expression of these factors likely reflects the target cell of transformation rather than being required for co...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5231408/ https://www.ncbi.nlm.nih.gov/pubmed/28080960 http://dx.doi.org/10.7554/eLife.19214 |
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author | Tenente, Inês M Hayes, Madeline N Ignatius, Myron S McCarthy, Karin Yohe, Marielle Sindiri, Sivasish Gryder, Berkley Oliveira, Mariana L Ramakrishnan, Ashwin Tang, Qin Chen, Eleanor Y Petur Nielsen, G Khan, Javed Langenau, David M |
author_facet | Tenente, Inês M Hayes, Madeline N Ignatius, Myron S McCarthy, Karin Yohe, Marielle Sindiri, Sivasish Gryder, Berkley Oliveira, Mariana L Ramakrishnan, Ashwin Tang, Qin Chen, Eleanor Y Petur Nielsen, G Khan, Javed Langenau, David M |
author_sort | Tenente, Inês M |
collection | PubMed |
description | Rhabdomyosarcoma (RMS) is a pediatric malignacy of muscle with myogenic regulatory transcription factors MYOD and MYF5 being expressed in this disease. Consensus in the field has been that expression of these factors likely reflects the target cell of transformation rather than being required for continued tumor growth. Here, we used a transgenic zebrafish model to show that Myf5 is sufficient to confer tumor-propagating potential to RMS cells and caused tumors to initiate earlier and have higher penetrance. Analysis of human RMS revealed that MYF5 and MYOD are mutually-exclusively expressed and each is required for sustained tumor growth. ChIP-seq and mechanistic studies in human RMS uncovered that MYF5 and MYOD bind common DNA regulatory elements to alter transcription of genes that regulate muscle development and cell cycle progression. Our data support unappreciated and dominant oncogenic roles for MYF5 and MYOD convergence on common transcriptional targets to regulate human RMS growth. DOI: http://dx.doi.org/10.7554/eLife.19214.001 |
format | Online Article Text |
id | pubmed-5231408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-52314082017-01-13 Myogenic regulatory transcription factors regulate growth in rhabdomyosarcoma Tenente, Inês M Hayes, Madeline N Ignatius, Myron S McCarthy, Karin Yohe, Marielle Sindiri, Sivasish Gryder, Berkley Oliveira, Mariana L Ramakrishnan, Ashwin Tang, Qin Chen, Eleanor Y Petur Nielsen, G Khan, Javed Langenau, David M eLife Cancer Biology Rhabdomyosarcoma (RMS) is a pediatric malignacy of muscle with myogenic regulatory transcription factors MYOD and MYF5 being expressed in this disease. Consensus in the field has been that expression of these factors likely reflects the target cell of transformation rather than being required for continued tumor growth. Here, we used a transgenic zebrafish model to show that Myf5 is sufficient to confer tumor-propagating potential to RMS cells and caused tumors to initiate earlier and have higher penetrance. Analysis of human RMS revealed that MYF5 and MYOD are mutually-exclusively expressed and each is required for sustained tumor growth. ChIP-seq and mechanistic studies in human RMS uncovered that MYF5 and MYOD bind common DNA regulatory elements to alter transcription of genes that regulate muscle development and cell cycle progression. Our data support unappreciated and dominant oncogenic roles for MYF5 and MYOD convergence on common transcriptional targets to regulate human RMS growth. DOI: http://dx.doi.org/10.7554/eLife.19214.001 eLife Sciences Publications, Ltd 2017-01-12 /pmc/articles/PMC5231408/ /pubmed/28080960 http://dx.doi.org/10.7554/eLife.19214 Text en http://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (http://creativecommons.org/publicdomain/zero/1.0/) . |
spellingShingle | Cancer Biology Tenente, Inês M Hayes, Madeline N Ignatius, Myron S McCarthy, Karin Yohe, Marielle Sindiri, Sivasish Gryder, Berkley Oliveira, Mariana L Ramakrishnan, Ashwin Tang, Qin Chen, Eleanor Y Petur Nielsen, G Khan, Javed Langenau, David M Myogenic regulatory transcription factors regulate growth in rhabdomyosarcoma |
title | Myogenic regulatory transcription factors regulate growth in rhabdomyosarcoma |
title_full | Myogenic regulatory transcription factors regulate growth in rhabdomyosarcoma |
title_fullStr | Myogenic regulatory transcription factors regulate growth in rhabdomyosarcoma |
title_full_unstemmed | Myogenic regulatory transcription factors regulate growth in rhabdomyosarcoma |
title_short | Myogenic regulatory transcription factors regulate growth in rhabdomyosarcoma |
title_sort | myogenic regulatory transcription factors regulate growth in rhabdomyosarcoma |
topic | Cancer Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5231408/ https://www.ncbi.nlm.nih.gov/pubmed/28080960 http://dx.doi.org/10.7554/eLife.19214 |
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