Regulation of the JMJD3 (KDM6B) histone demethylase in glioblastoma stem cells by STAT3

被引:48
|
作者
Sherry-Lynes, Maureen M.
Sengupta, Sejuti
Kulkarni, Shreya
Cochran, Brent H. [1 ]
机构
[1] Tufts Univ, Sch Med, Sackler Sch Grad Biomed Sci, Grad Program Cell & Mol Physiol, Boston, MA 02111 USA
来源
PLOS ONE | 2017年 / 12卷 / 04期
关键词
GENE-EXPRESSION; H3K27; DEMETHYLASE; INK4A/ARF LOCUS; SELF-RENEWAL; CANCER; DIFFERENTIATION; METHYLATION; ACTIVATION; TARGET; EZH2;
D O I
10.1371/journal.pone.0174775
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
The growth factor and cytokine regulated transcription factor STAT3 is required for the self-renewal of several stem cell types including tumor stem cells from glioblastoma. Here we show that STAT3 inhibition leads to the upregulation of the histone H3K27me2/3 demethylase Jmjd3 (KDM6B), which can reverse polycomb complex-mediated repression of tissue specific genes. STAT3 binds to the Jmjd3 promoter, suggesting that Jmjd3 is a direct target of STAT3. Overexpression of Jmjd3 slows glioblastoma stem cell growth and neurosphere formation, whereas knockdown of Jmjd3 rescues the STAT3 inhibitor-induced neurosphere formation defect. Consistent with this observation, STAT3 inhibition leads to histone H3K27 demethylation of neural differentiation genes, such as Myt1, FGF21, and GDF15. These results demonstrate that the regulation of Jmjd3 by STAT3 maintains repression of differentiation specific genes and is therefore important for the maintenance of self-renewal of normal neural and glioblastoma stem cells.
引用
收藏
页数:17
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