EZH2型
癌症研究
甲基化
组蛋白甲基转移酶
生物
表观遗传学
转移
甲基转移酶
癌症
组蛋白甲基化
DNA甲基化
遗传学
基因表达
基因
作者
Peng Wang,Liang Zhao,Yiqi Rui,Yongbin Ding
标识
DOI:10.1038/s41417-022-00535-5
摘要
SET and MYND domain-containing protein 3 (SMYD3), a known histone methyltransferase, was reported to regulate cancer pathogenesis. However, its role in gastric development and progression remains unclear. EZH2 methylation had been associated with cancer metastasis, but the EZH2 methylation status in gastric cancer (GC) is unknown. Here, we report that EZH2 K421 methylation was responsible for gastric cancer cell soft agar colony formation, in vivo metastasis, and macrophage polarization. Mechanically, we identified SMYD3 as the methyltransferase of EZH2 at K421 residue which accelerates EZH2 Ubiquitin proteasome degradation. Cell harboring non-methylated EZH2 mutants promotes gastric cancer cell metastasis. Taken together, our results showed that SMYD3-EZH2 axis restricts gastric cancer metastasis via integrating epigenetic signaling.
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