经m6A修饰的circCCAR1通过增强肝细胞癌中的KIF5B表达来促进恶性扩散
Jiayu Chen1, Zhuolin Zhou1, Yang Shen1
1Cancer Center, Renmin Hospital of Wuhan University, No.99, Zhangzhidong Road, Wuhan, 430060, Hubei, China.
Journal of physiology and biochemistry
|July 22, 2025
概括
循环RNA细胞分裂周期和细胞亡调节器1 (circCCAR1) 通过通过miR-641轴稳定基因素家族成员5B (KIF5B) mRNA,促进肝细胞癌 (HCC) 的进展. 沉默cirCCAR1可以抑制HCC的生长.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
背景情况:
- 肝细胞癌 (HCC) 呈现出侵略性行为和高死亡率.
- 循环RNAs (circRNAs) 与癌症有关,但circCCAR1在HCC中的作用尚不清楚.
研究的目的:
- 为了阐明circCCAR1在HCC进展中的机制.
- 为了研究circCCAR1,miR-641和KIF5B在HCC中的相互作用.
主要方法:
- 在HCC和正常细胞中量化circCCAR1,miR-641和KIF5B的表达.
- 涉及RNA甲基转移酶YTHDC1,m6A修饰和RNA结合蛋白PTBP1.1.的机制研究.
- 在体内异种移植小鼠模型,以评估circCCAR1操纵后的瘤生长.
主要成果:
- 在HCC中,circCCAR1显著过度表达.
- YTHDC1促进了m6A修饰的cirCCAR1.1从核到细胞质的传输.
- circCCAR1 刺激miR-641,上调KIF5B,促进HCC细胞增殖和瘤生长.
结论:
- 通过YTHDC1介导的m6A-circCCAR1传输促进了HCC的进展.
- circCCAR1通过miR-641/KIF5B通路增强了HCC的发展.
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