基因敲除
自噬
癌症研究
下调和上调
转移
STAT蛋白
癌症
小RNA
细胞生物学
体内
环状RNA
癌细胞
生物
PI3K/AKT/mTOR通路
车站3
激活剂(遗传学)
细胞生长
糖酵解
转录因子
核糖核酸
瓦博格效应
长非编码RNA
TFEB
基因沉默
信号转导
厌氧糖酵解
抄写(语言学)
癌变
细胞培养
细胞凋亡
受体
生物化学
基因
生物技术
遗传学
作者
Jing Yang,Xing Zhang,Jiacheng Cao,Penghui Xu,Zetian Chen,Sen Wang,Bowen Li,Lu Zhang,Li Xie,Lang Fang,Zekuan Xu
标识
DOI:10.1038/s41419-021-04216-3
摘要
Gastric cancer remains the third leading cause of cancer-related mortality worldwide. Emerging evidence has shown that circular RNAs (circRNAs) play a critical regulatory role in the occurrence and development of various cancers through sponging miRNAs or acting as RNA-binding protein (RBP) sponges. We found that circUBE2Q2 was significantly upregulated in GC tissues and cell lines. Knockdown of circUBE2Q2 inhibited proliferation, migration, invasion, and glycolysis, and increased autophagy in vitro. In addition, knockdown of circUBE2Q2 inhibited GC tumorigenicity and metastasis potential in vivo. A series of experiments were performed to confirm that circUBE2Q2 regulates GC progression via the circUBE2Q2-miR-370-3p-STAT3 axis and promotes tumor metastasis through exosomal communication. Further in vivo experiments confirmed that, combination treatment of circUBE2Q2 knocking down and STAT3 inhibitor has synergistic effects on the gastric cancer growth inhibition, which provides a possibility to enhance the sensitivity of targeted drugs to gastric cancer through targeting circUBE2Q2. Our findings revealed that circUBE2Q2 may serve as a new proliferation-promoting factor and prognostic marker in gastric cancer.
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