血管内皮生长因子
车站3
DNMT1型
癌症研究
新生血管
生物
基因表达
血管内皮生长因子A
分子生物学
下调和上调
化学
血管生成
DNA甲基化
细胞生物学
基因
磷酸化
血管内皮生长因子受体
生物化学
作者
Huanyu Zhao,Yipan Zhu,Wen Ye,Xinyu Ding,Jing Ping Sun,Ren-Peng Ji,Qiuju Han,Lu-Yuan Li
标识
DOI:10.1016/j.bcp.2022.115334
摘要
Monocyte chemotactic protein-1 (MCP-1) is known to be able to facilitate vascular endothelial growth factor (VEGF) gene expression, hence promoting vascular hyperpermeability and neovascularization. We show here that a microRNA molecule, miR-374b-5p can target the 3′-untranslated region of the VEGF mRNA, thus preventing VEGF production. Additionally, MCP-1 promotes the acetylation of transcription factor stat3 at Lys685, which facilitates the formation of an ac-stat3-DNA methyltransferase-histone methyltransferase complex (ac-stat3/DNMT1/EZH2) that binds to the promoter of the miR-374b-5p gene. This results in diminished miR-374b-5p expression and enhanced VEGF production. Moreover, treatment of appropriate animal models either with a miR-374b-5p mimicry or with inhibitors of either stat3 acetylation, DNMT1, or EZH2, leads to marked inhibition of MCP-1-promoted neovascularization and tumor growth. These findings indicate that MCP-1 facilitated inhibition of miR-374b-5p gene expression leads to the removal of a block of VEGF mRNA translation by miR-374b-5p. This mechanism could be of importance in the modulation of inflammatory conditions.
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