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SIX1 and EWS/FLI1 co-regulate an anti-metastatic gene network in Ewing Sarcoma
Ewing sarcoma (ES), which is characterized by the presence of oncogenic fusion proteins such as EWS/FLI1, is an aggressive pediatric malignancy with a high rate of early dissemination and poor outcome after distant spread. Here we demonstrate that the SIX1 homeoprotein, which enhances metastasis in...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356808/ https://www.ncbi.nlm.nih.gov/pubmed/37468459 http://dx.doi.org/10.1038/s41467-023-39945-w |
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author | Hughes, Connor J. Fields, Kaiah M. Danis, Etienne P. Hsu, Jessica Y. Neelakantan, Deepika Vincent, Melanie Y. Gustafson, Annika L. Oliphant, Michael J. Sreekanth, Varsha Zaberezhnyy, Vadym Costello, James C. Jedlicka, Paul Ford, Heide L. |
author_facet | Hughes, Connor J. Fields, Kaiah M. Danis, Etienne P. Hsu, Jessica Y. Neelakantan, Deepika Vincent, Melanie Y. Gustafson, Annika L. Oliphant, Michael J. Sreekanth, Varsha Zaberezhnyy, Vadym Costello, James C. Jedlicka, Paul Ford, Heide L. |
author_sort | Hughes, Connor J. |
collection | PubMed |
description | Ewing sarcoma (ES), which is characterized by the presence of oncogenic fusion proteins such as EWS/FLI1, is an aggressive pediatric malignancy with a high rate of early dissemination and poor outcome after distant spread. Here we demonstrate that the SIX1 homeoprotein, which enhances metastasis in most tumor types, suppresses ES metastasis by co-regulating EWS/FLI1 target genes. Like EWS/FLI1, SIX1 promotes cell growth/transformation, yet dramatically inhibits migration and invasion, as well as metastasis in vivo. We show that EWS/FLI1 promotes SIX1 protein expression, and that the two proteins share genome-wide binding profiles and transcriptional regulatory targets, including many metastasis-associated genes such as integrins, which they co-regulate. We further show that SIX1 downregulation of integrins is critical to its ability to inhibit invasion, a key characteristic of metastatic cells. These data demonstrate an unexpected anti-metastatic function for SIX1, through coordinate gene regulation with the key oncoprotein in ES, EWS/FLI1. |
format | Online Article Text |
id | pubmed-10356808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103568082023-07-21 SIX1 and EWS/FLI1 co-regulate an anti-metastatic gene network in Ewing Sarcoma Hughes, Connor J. Fields, Kaiah M. Danis, Etienne P. Hsu, Jessica Y. Neelakantan, Deepika Vincent, Melanie Y. Gustafson, Annika L. Oliphant, Michael J. Sreekanth, Varsha Zaberezhnyy, Vadym Costello, James C. Jedlicka, Paul Ford, Heide L. Nat Commun Article Ewing sarcoma (ES), which is characterized by the presence of oncogenic fusion proteins such as EWS/FLI1, is an aggressive pediatric malignancy with a high rate of early dissemination and poor outcome after distant spread. Here we demonstrate that the SIX1 homeoprotein, which enhances metastasis in most tumor types, suppresses ES metastasis by co-regulating EWS/FLI1 target genes. Like EWS/FLI1, SIX1 promotes cell growth/transformation, yet dramatically inhibits migration and invasion, as well as metastasis in vivo. We show that EWS/FLI1 promotes SIX1 protein expression, and that the two proteins share genome-wide binding profiles and transcriptional regulatory targets, including many metastasis-associated genes such as integrins, which they co-regulate. We further show that SIX1 downregulation of integrins is critical to its ability to inhibit invasion, a key characteristic of metastatic cells. These data demonstrate an unexpected anti-metastatic function for SIX1, through coordinate gene regulation with the key oncoprotein in ES, EWS/FLI1. Nature Publishing Group UK 2023-07-19 /pmc/articles/PMC10356808/ /pubmed/37468459 http://dx.doi.org/10.1038/s41467-023-39945-w 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Hughes, Connor J. Fields, Kaiah M. Danis, Etienne P. Hsu, Jessica Y. Neelakantan, Deepika Vincent, Melanie Y. Gustafson, Annika L. Oliphant, Michael J. Sreekanth, Varsha Zaberezhnyy, Vadym Costello, James C. Jedlicka, Paul Ford, Heide L. SIX1 and EWS/FLI1 co-regulate an anti-metastatic gene network in Ewing Sarcoma |
title | SIX1 and EWS/FLI1 co-regulate an anti-metastatic gene network in Ewing Sarcoma |
title_full | SIX1 and EWS/FLI1 co-regulate an anti-metastatic gene network in Ewing Sarcoma |
title_fullStr | SIX1 and EWS/FLI1 co-regulate an anti-metastatic gene network in Ewing Sarcoma |
title_full_unstemmed | SIX1 and EWS/FLI1 co-regulate an anti-metastatic gene network in Ewing Sarcoma |
title_short | SIX1 and EWS/FLI1 co-regulate an anti-metastatic gene network in Ewing Sarcoma |
title_sort | six1 and ews/fli1 co-regulate an anti-metastatic gene network in ewing sarcoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356808/ https://www.ncbi.nlm.nih.gov/pubmed/37468459 http://dx.doi.org/10.1038/s41467-023-39945-w |
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