环状RNA FGGY在肝癌中的表达及其对HepG2细胞铁死亡的影响
喻言, 钟红珊中国医科大学附属第一医院介入治疗科, 沈阳 110001
收稿日期:
2022-03-30出版日期:
2022-12-30发布日期:
2022-12-12通讯作者:
钟红珊E-mail:hszhong@cmu.edu.cn作者简介:
喻言 (1997-),男,博士研究生.基金资助:
国家重点研发计划(2018YFC0115500);辽宁省兴辽英才计划(XLYC1802098)关键词: 肝癌, RNA结合蛋白, 环状RNA, m6A甲基化, 铁死亡
Abstract: Objective To study the expression of FGGY circular RNA(circRNA) in liver cancer, its effect on ferroptosis in HepG2 cells, and its related mechanism. Methods Real-time PCR detected the expression of circFGGY in normal liver cells and HepG2 liver cancer cells. RNA immunoprecipitation(IP) was used to detect the binding of MSI2 and circFGGY, and binding of circFGGY and FSP1. Methylated RNA IP(MeRIP) was used to detect binding of METTL3 and circFGGY. CCK8, lipid mass peroxide, glutathione, and iron assays, C11-BODIPY staining, and flow cytometry were used to detect the effect of silencing circFGGY on ferroptosis in HepG2 cells. The effect of silencing circFGGY on FSP1 protein expression was detected by Western blotting method. Results circFGGY was highly expressed in hepatoma cells. Exogenous knockdown of circFGGY expression promoted ferroptosis in HepG2 cells. MSI2 bound to and promoted the formation of circFGGY. High expression of METTL3 promoted circFGGY m6A methylation modification and its nucleoplasmic redistribution. Conclusion MSI2 promotes the formation of circFGGY. The nuclear export of circFGGY with increased m6A methylation regulates the expression of FSP1 protein and ferroptosis in HepG2 cells.
Key words: hepatocellular carcinoma, RNA binding protein, circular RNA, m6A methylation, ferroptosis
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