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

被引:78
|
作者
Karakashev, Sergey [1 ]
Zhu, Hengrui
Wu, Shuai [1 ]
Yokoyama, Yuhki [1 ]
Bitler, Benjamin G. [1 ]
Park, Pyoung-Hwa [1 ]
Lee, Jeong-Heon [2 ]
Kossenkov, Andrew V. [3 ]
Gaonkar, Krutika Satish [4 ]
Yan, Huihuang [4 ]
Drapkin, Ronny [5 ]
Conejo-Garcia, Jose R. [6 ]
Speicher, David W. [7 ]
Ordog, Tamas [2 ]
Zhang, Rugang [1 ]
机构
[1] Wistar Inst Anat & Biol, Gene Express & Regulat Program, Philadelphia, PA 19104 USA
[2] Mayo Clin, Ctr Individualized Med, Epigenom Program, Rochester, MN 55905 USA
[3] Wistar Inst Anat & Biol, Ctr Syst & Computat Biol, Philadelphia, PA 19104 USA
[4] Mayo Clin, Dept Hlth Sci Res, Div Biostat & Informat, Rochester, MN 55905 USA
[5] Univ Penn, Perelman Sch Med, Dept Obstet & Gynecol, Philadelphia, PA 19104 USA
[6] H Lee Moffitt Canc Ctr & Res Inst, Dept Immunol, Tampa, FL 33612 USA
[7] Wistar Inst Anat & Biol, Mol & Cellular Oncol Program, Philadelphia, PA 19104 USA
来源
NATURE COMMUNICATIONS | 2018年 / 9卷
基金
美国国家卫生研究院;
关键词
EXPRESSION; CARM1; GENE; COACTIVATOR; SENESCENCE; METHYLATION; CARCINOMA; CELLS; HETEROCHROMATIN; METABOLISM;
D O I
10.1038/s41467-018-03031-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页数:11
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