缺氧增加了IGF2BP3结合的圆形RNAs的生物发生
Kriti Kaushik1, Hemant Kumar1, Samriddhi Mehta2
1Department of Biochemistry, All India Institute of Medical Sciences, Ansari Nagar, Convergence Block, New Delhi, 110029, India.
Molecular biology reports
|February 8, 2024
概括
缺氧会增加循环RNA (circRNA) 的产生,可能导致瘤的进展. 这项研究研究了胰岛素样生长因子2结合蛋白3 (IGF2BP3) 和 (QKI) 在缺氧诱导的circRNA生物发生中的作用.
科学领域:
- 分子生物学分子生物学
- 癌症研究 癌症研究
- 在RNA生物学,RNA生物学.
背景情况:
- 胰岛素样生长因子2结合蛋白3 (IGF2BP3) 通过与各种RNAs相互作用,与癌症进展有关.
- 缺氧是瘤中常见的特征,可调节缺氧诱导因素并促进瘤生长.
- 由低氧诱导的Quaking (QKI) 基因增强了表皮细胞到介质细胞的过渡 (EMT) 和循环RNA (circRNA) 生产.
研究的目的:
- 在低氧条件下研究IGF2BP3,QKI,circRNA及其宿主基因之间的轴.
- 了解IGF2BP3和QKI在缺氧诱导的circRNA生物发生中的作用及其对瘤进展的贡献.
主要方法:
- 使用定量实时PCR (qRT-PCR) 来评估IGF2BP3,QKI,EMT标记物,circRNA和宿主mRNA的表达.
- RNA免疫沉 (RIP) 测定证实了IGF2BP3与特定circRNAs的结合.
- 细胞系 (HeLa,HepG2,U87MG) 在正常和缺氧条件下进行培养,以分析基因表达变化.
主要成果:
- 缺氧高调低氧标志物 (VEGF,CA9) 和所有细胞系中的SNAIL.
- 在缺氧下,IGF2BP3和QKI的表达增加,这表明它们参与circRNA生物发生和稳定.
- 六个宿主基因 (PHC3,CDYL,ANKRD17,ARID1A,NEIL3,FNDC3B) 在低氧状态下显示mRNA和circRNA的表达增加,这表明在瘤启动中具有协同作用.
- 在缺氧下,大多数基因和时间点的circRNA与mRNA表达比率增加.
结论:
- 缺氧可以增强circRNA生物发生.
- 在缺氧下观察到的circRNA产量的增加可能会导致瘤的进展.
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