在circ-EIF4A3和EIF4A3之间的调控反循环 增强肠直肠癌细胞的自和生长
Qingke Li1, Zhiwu Wang2, Jian Wang1
1Department of Gastrointestinal Surgery, Tangshan People's Hospital, Tangshan 063000, Hebei, China.
Translational oncology
|May 25, 2024
概括
循环RNAs (circRNAs) 和真核转化启动因子4A3 (EIF4A3) 促进结直肠癌 (CRC) 的生长. 涉及circEIF4A3和EIF4A3的反循环可以增强CRC细胞自和增殖.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
背景情况:
- 循环RNAs (circRNAs) 在结直肠癌 (CRC) 进展中起着重要作用.
- 细胞转化启动因子4A3 (EIF4A3) 参与促进circRNA生物发生.
- 在CRC细胞自中,EIF4A3衍生的circRNA (circEIF4A3) 的特定功能尚不清楚.
研究的目的:
- 为了研究circEIF4A3对结直肠癌细胞生长和自的影响.
- 阐明circEIF4A3在CRC中的作用背后的分子机制.
主要方法:
- 研究了EIF4A3和circEIF4A3对CRC细胞增殖的协同作用.
- 分析了circEIF4A3,miR-3126-5p和EIF4A3表达之间的相互作用.
- 通过circEIF4A3和EIF4A3.3.3检查了与自相关的基因 (ATG5,ATG7) 和二化酶 (USP14) 的调节.
- 评估了CRC细胞中EIF4A3和circEIF4A3形成之间的反机制.
主要成果:
- 发现EIF4A3和circEIF4A3可以协同促进CRC细胞生长.
- 证明CircEIF4A3可以封存miR-3126-5p,从而导致EIF4A3表达的增加.
- CircEIF4A3增强了EIF4A3的表达,通过稳定ATG5mRNA促进了自,并通过USP14mRNA稳定增强了ATG7蛋白的稳定性.
- 提高ATG5和ATG7表达的调节抵消了EIF4A3淘汰的增长抑制作用.
- 已经证明EIF4A3可以诱导CRC细胞中的circEIF4A3形成.
结论:
- 在结直肠癌中,circEIF4A3和EIF4A3之间存在正反循环.
- 这种反循环通过增强细胞自来支持CRC细胞生长.
- CircEIF4A3和EIF4A3代表了结直肠癌治疗的潜在治疗点.
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