Circular RNA_101237 mediates anoxia/reoxygenation injury by targeting let-7a-5p/IGF2BP3 in cardiomyocytes

被引:44
作者
Gan, Jianting [1 ]
Yuan, Jun [1 ]
Liu, Yu [1 ]
Lu, Zhengde [1 ]
Xue, Yan [1 ]
Shi, Lei [1 ]
Zeng, Huayuan [1 ]
机构
[1] Peoples Hosp Guangxi Zhuang Autonomous Reg, Dept Cardiol, 6 Taoyuan Rd, Nanning 530021, Guangxi Zhuang, Peoples R China
关键词
circular RNA; anoxia; reoxygenation; cardiovascular disease; let-7; insulin-like growth factor 2 mRNA-binding protein 3; CARDIOVASCULAR-DISEASE; MICRORNAS; HEART; EXPRESSION; LET-7; RNAS; APOPTOSIS; AUTOPHAGY; PROTECTS; PATHWAY;
D O I
10.3892/ijmm.2019.4441
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Circular RNAs (circRNAs) serve important roles in cardiovascular diseases, including myocardial infarction. However, the mechanisms underlying the roles of circRNAs in cardiomyocyte death induced by anoxia/reoxygenation (A/R) are not fully understood. In the present study, the roles of circRNA_101237 and let-7a-5p in cardiomyocyte death induced by A/R injury were investigated. It was identified that circRNA_101237 was induced by A/R injury in a time-dependent manner and that circRNA_101237 knockdown protected cardiomyocytes from A/R-mediated apoptosis. Additional mechanistic studies revealed that circRNA_101237 served as a sponge for let-7a-5p, subsequently regulating insulin-like growth factor 2 mRNA-binding protein 3 (IGF2BP3)-dependent autophagy. IGF2BP3 downregulation decreased the levels of apoptosis and inhibited autophagy induced by A/R challenge in primary cardiomyocytes. These results identified circRNA_101237 as a novel circRNA that regulates cardiomyocyte death and autophagy, and demonstrated that the circRNA-101237/let-7a-5p/IGF2BP3 axis, which serves as a regulator of cardiomyocyte death, may be a potential therapeutic target for the management of cardiovascular diseases.
引用
收藏
页码:451 / 460
页数:10
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