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The histone demethylase PHF8 regulates TGFβ signaling and promotes melanoma metastasis
The contribution of epigenetic dysregulation to metastasis remains understudied. Through a meta-analysis of gene expression datasets followed by a mini-screen, we identified Plant Homeodomain Finger protein 8 (PHF8), a histone demethylase of the Jumonji C protein family, as a previously unidentified...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8856617/ https://www.ncbi.nlm.nih.gov/pubmed/35179962 http://dx.doi.org/10.1126/sciadv.abi7127 |
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author | Moubarak, Rana S. de Pablos-Aragoneses, Ana Ortiz-Barahona, Vanessa Gong, Yixiao Gowen, Michael Dolgalev, Igor Shadaloey, Sorin A. A. Argibay, Diana Karz, Alcida Von Itter, Richard Vega-Sáenz de Miera, Eleazar Carmelo Sokolova, Elena Darvishian, Farbod Tsirigos, Aristotelis Osman, Iman Hernando, Eva |
author_facet | Moubarak, Rana S. de Pablos-Aragoneses, Ana Ortiz-Barahona, Vanessa Gong, Yixiao Gowen, Michael Dolgalev, Igor Shadaloey, Sorin A. A. Argibay, Diana Karz, Alcida Von Itter, Richard Vega-Sáenz de Miera, Eleazar Carmelo Sokolova, Elena Darvishian, Farbod Tsirigos, Aristotelis Osman, Iman Hernando, Eva |
author_sort | Moubarak, Rana S. |
collection | PubMed |
description | The contribution of epigenetic dysregulation to metastasis remains understudied. Through a meta-analysis of gene expression datasets followed by a mini-screen, we identified Plant Homeodomain Finger protein 8 (PHF8), a histone demethylase of the Jumonji C protein family, as a previously unidentified prometastatic gene in melanoma. Loss- and gain-of-function approaches demonstrate that PHF8 promotes cell invasion without affecting proliferation in vitro and increases dissemination but not subcutaneous tumor growth in vivo, thus supporting its specific contribution to the acquisition of metastatic potential. PHF8 requires its histone demethylase activity to enhance melanoma cell invasion. Transcriptomic and epigenomic analyses revealed that PHF8 orchestrates a molecular program that directly controls the TGFβ signaling pathway and, as a consequence, melanoma invasion and metastasis. Our findings bring a mechanistic understanding of epigenetic regulation of metastatic fitness in cancer, which may pave the way for improved therapeutic interventions. |
format | Online Article Text |
id | pubmed-8856617 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-88566172022-03-04 The histone demethylase PHF8 regulates TGFβ signaling and promotes melanoma metastasis Moubarak, Rana S. de Pablos-Aragoneses, Ana Ortiz-Barahona, Vanessa Gong, Yixiao Gowen, Michael Dolgalev, Igor Shadaloey, Sorin A. A. Argibay, Diana Karz, Alcida Von Itter, Richard Vega-Sáenz de Miera, Eleazar Carmelo Sokolova, Elena Darvishian, Farbod Tsirigos, Aristotelis Osman, Iman Hernando, Eva Sci Adv Biomedicine and Life Sciences The contribution of epigenetic dysregulation to metastasis remains understudied. Through a meta-analysis of gene expression datasets followed by a mini-screen, we identified Plant Homeodomain Finger protein 8 (PHF8), a histone demethylase of the Jumonji C protein family, as a previously unidentified prometastatic gene in melanoma. Loss- and gain-of-function approaches demonstrate that PHF8 promotes cell invasion without affecting proliferation in vitro and increases dissemination but not subcutaneous tumor growth in vivo, thus supporting its specific contribution to the acquisition of metastatic potential. PHF8 requires its histone demethylase activity to enhance melanoma cell invasion. Transcriptomic and epigenomic analyses revealed that PHF8 orchestrates a molecular program that directly controls the TGFβ signaling pathway and, as a consequence, melanoma invasion and metastasis. Our findings bring a mechanistic understanding of epigenetic regulation of metastatic fitness in cancer, which may pave the way for improved therapeutic interventions. American Association for the Advancement of Science 2022-02-18 /pmc/articles/PMC8856617/ /pubmed/35179962 http://dx.doi.org/10.1126/sciadv.abi7127 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). 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 use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Moubarak, Rana S. de Pablos-Aragoneses, Ana Ortiz-Barahona, Vanessa Gong, Yixiao Gowen, Michael Dolgalev, Igor Shadaloey, Sorin A. A. Argibay, Diana Karz, Alcida Von Itter, Richard Vega-Sáenz de Miera, Eleazar Carmelo Sokolova, Elena Darvishian, Farbod Tsirigos, Aristotelis Osman, Iman Hernando, Eva The histone demethylase PHF8 regulates TGFβ signaling and promotes melanoma metastasis |
title | The histone demethylase PHF8 regulates TGFβ signaling and promotes melanoma metastasis |
title_full | The histone demethylase PHF8 regulates TGFβ signaling and promotes melanoma metastasis |
title_fullStr | The histone demethylase PHF8 regulates TGFβ signaling and promotes melanoma metastasis |
title_full_unstemmed | The histone demethylase PHF8 regulates TGFβ signaling and promotes melanoma metastasis |
title_short | The histone demethylase PHF8 regulates TGFβ signaling and promotes melanoma metastasis |
title_sort | histone demethylase phf8 regulates tgfβ signaling and promotes melanoma metastasis |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8856617/ https://www.ncbi.nlm.nih.gov/pubmed/35179962 http://dx.doi.org/10.1126/sciadv.abi7127 |
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