血管生成拟态
雅普1
基因敲除
甲基化
血管生成
河马信号通路
信使核糖核酸
癌症研究
生物
DNA甲基化
N6-甲基腺苷
细胞生物学
癌症
信号转导
甲基转移酶
细胞培养
转移
遗传学
基因
基因表达
转录因子
作者
Kailiang Qiao,Yantao Liu,Zheng Xu,Haohao Zhang,Heng Zhang,Chao Zhang,Zhi Chang,Xinyan Lu,Zhongwei Li,Ce Luo,Yanrong Liu,Cheng Yang,Tao Sun
出处
期刊:Angiogenesis
[Springer Science+Business Media]
日期:2020-09-13
卷期号:24 (1): 83-96
被引量:121
标识
DOI:10.1007/s10456-020-09744-8
摘要
Vasculogenic mimicry (VM) formed by aggressive tumor cells to mimic vasculogenic networks plays an important role in the tumor malignancy of HCC. However, the pathogenesis underlying VM is complex and has not been fully defined. m6A is a common mRNA modification and has many biological effects. However, the relationship between m6A and VM remains unclear. In this research, we found that m6A methyltransferase METTL3 in HCC tissues was positively correlated with VM. The m6A level of mRNA significantly increased in 3D cultured cells treated with VEGFa and was related to VM formation. Transcriptome sequencing analysis of 3D cultured cells with knockdown Mettl3 showed that the Hippo pathway was involved in m6A-mediated VM formation. Further mechanism research indicated that the m6A modification of YAP1 mRNA affected the translation of YAP1 mRNA. In conclusion, m6A methylation plays a key role in VM formation in HCC. METTL3 and YAP1 could be potential therapeutic targets via impairing VM formation in anti-metastatic strategies.
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