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CARM1-expressing ovarian cancer depends on the histone methyltransferase EZH2 activity

CARM1 is an arginine methyltransferase that asymmetrically dimethylates protein substrates on arginine residues. CARM1 is often overexpressed in human cancers. However, clinically applicable cancer therapeutic strategies based on CARM1 expression remain to be explored. Here, we report that EZH2 inhi...

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Autores principales: Karakashev, Sergey, Zhu, Hengrui, Wu, Shuai, Yokoyama, Yuhki, Bitler, Benjamin G., Park, Pyoung-Hwa, Lee, Jeong-Heon, Kossenkov, Andrew V., Gaonkar, Krutika Satish, Yan, Huihuang, Drapkin, Ronny, Conejo-Garcia, Jose R., Speicher, David W., Ordog, Tamas, Zhang, Rugang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5809368/
https://www.ncbi.nlm.nih.gov/pubmed/29434212
http://dx.doi.org/10.1038/s41467-018-03031-3
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author Karakashev, Sergey
Zhu, Hengrui
Wu, Shuai
Yokoyama, Yuhki
Bitler, Benjamin G.
Park, Pyoung-Hwa
Lee, Jeong-Heon
Kossenkov, Andrew V.
Gaonkar, Krutika Satish
Yan, Huihuang
Drapkin, Ronny
Conejo-Garcia, Jose R.
Speicher, David W.
Ordog, Tamas
Zhang, Rugang
author_facet Karakashev, Sergey
Zhu, Hengrui
Wu, Shuai
Yokoyama, Yuhki
Bitler, Benjamin G.
Park, Pyoung-Hwa
Lee, Jeong-Heon
Kossenkov, Andrew V.
Gaonkar, Krutika Satish
Yan, Huihuang
Drapkin, Ronny
Conejo-Garcia, Jose R.
Speicher, David W.
Ordog, Tamas
Zhang, Rugang
author_sort Karakashev, Sergey
collection PubMed
description CARM1 is an arginine methyltransferase that asymmetrically dimethylates protein substrates on arginine residues. CARM1 is often overexpressed in human cancers. However, clinically applicable cancer therapeutic strategies based on CARM1 expression remain to be explored. Here, we report that EZH2 inhibition is effective in CARM1-expressing epithelial ovarian cancer. Inhibition of EZH2 activity using a clinically applicable small molecule inhibitor significantly suppresses the growth of CARM1-expressing, but not CARM1-deficient, ovarian tumors in two xenograft models and improves the survival of mice bearing CARM1-expressing ovarian tumors. The observed selectivity correlates with reactivation of EZH2 target tumor suppressor genes in a CARM1-dependent manner. Mechanistically, CARM1 promotes EZH2-mediated silencing of EZH2/BAF155 target tumor suppressor genes by methylating BAF155, which leads to the displacement of BAF155 by EZH2. Together, these results indicate that pharmacological inhibition of EZH2 represents a novel therapeutic strategy for CARM1-expressing cancers.
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spelling pubmed-58093682018-02-14 CARM1-expressing ovarian cancer depends on the histone methyltransferase EZH2 activity Karakashev, Sergey Zhu, Hengrui Wu, Shuai Yokoyama, Yuhki Bitler, Benjamin G. Park, Pyoung-Hwa Lee, Jeong-Heon Kossenkov, Andrew V. Gaonkar, Krutika Satish Yan, Huihuang Drapkin, Ronny Conejo-Garcia, Jose R. Speicher, David W. Ordog, Tamas Zhang, Rugang Nat Commun Article CARM1 is an arginine methyltransferase that asymmetrically dimethylates protein substrates on arginine residues. CARM1 is often overexpressed in human cancers. However, clinically applicable cancer therapeutic strategies based on CARM1 expression remain to be explored. Here, we report that EZH2 inhibition is effective in CARM1-expressing epithelial ovarian cancer. Inhibition of EZH2 activity using a clinically applicable small molecule inhibitor significantly suppresses the growth of CARM1-expressing, but not CARM1-deficient, ovarian tumors in two xenograft models and improves the survival of mice bearing CARM1-expressing ovarian tumors. The observed selectivity correlates with reactivation of EZH2 target tumor suppressor genes in a CARM1-dependent manner. Mechanistically, CARM1 promotes EZH2-mediated silencing of EZH2/BAF155 target tumor suppressor genes by methylating BAF155, which leads to the displacement of BAF155 by EZH2. Together, these results indicate that pharmacological inhibition of EZH2 represents a novel therapeutic strategy for CARM1-expressing cancers. Nature Publishing Group UK 2018-02-12 /pmc/articles/PMC5809368/ /pubmed/29434212 http://dx.doi.org/10.1038/s41467-018-03031-3 Text en © The Author(s) 2018 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/.
spellingShingle Article
Karakashev, Sergey
Zhu, Hengrui
Wu, Shuai
Yokoyama, Yuhki
Bitler, Benjamin G.
Park, Pyoung-Hwa
Lee, Jeong-Heon
Kossenkov, Andrew V.
Gaonkar, Krutika Satish
Yan, Huihuang
Drapkin, Ronny
Conejo-Garcia, Jose R.
Speicher, David W.
Ordog, Tamas
Zhang, Rugang
CARM1-expressing ovarian cancer depends on the histone methyltransferase EZH2 activity
title CARM1-expressing ovarian cancer depends on the histone methyltransferase EZH2 activity
title_full CARM1-expressing ovarian cancer depends on the histone methyltransferase EZH2 activity
title_fullStr CARM1-expressing ovarian cancer depends on the histone methyltransferase EZH2 activity
title_full_unstemmed CARM1-expressing ovarian cancer depends on the histone methyltransferase EZH2 activity
title_short CARM1-expressing ovarian cancer depends on the histone methyltransferase EZH2 activity
title_sort carm1-expressing ovarian cancer depends on the histone methyltransferase ezh2 activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5809368/
https://www.ncbi.nlm.nih.gov/pubmed/29434212
http://dx.doi.org/10.1038/s41467-018-03031-3
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