Circ1811 suppresses gastric cancer progression by regulating the miR-632/ DAPK1 axis

被引:3
作者
Fu, Min [1 ,2 ]
Gu, Jianmei [3 ]
Yu, Dan [2 ]
Wang, Maoye [2 ]
Zhang, Jiahui [2 ]
Ji, Runbi [1 ]
Jiang, Pengcheng [1 ]
Zhang, Xu [1 ,2 ]
机构
[1] Jiangsu Univ, Inst Digest Dis, Affiliated Peoples Hosp, Zhenjiang 212002, Jiangsu, Peoples R China
[2] Jiangsu Univ, Sch Med, Jiangsu Key Lab Med Sci & Lab Med, Zhenjiang 212013, Jiangsu, Peoples R China
[3] Nantong Univ, Nantong Tumor Hosp, Departmemt Clin Lab Med, Affiliated Tumor Hosp, Nantong 226361, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Circular RNA; Gastric cancer; Cell proliferation; Migration; ceRNA;
D O I
10.1016/j.gene.2024.148331
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Compelling evidence has identified circRNAs as crucial regulators in initiation and progression of various cancers, including gastric cancer (GC). However, the function and regulatory mechanisms of circRNAs in GC remain largely unknown. In this study, attention is paid to a novel circular RNA circ1811, which exerts significant downregulated expression in GC tissues compared with adjacent non-cancerous tissues. The expression of circ1811 in GC tumor tissues is negatively correlated with the extent of lymphatic metastasis in GC patients. Overexpression of circ1811 inhibited GC cell proliferation, migration and invasion while promoting apoptosis, whereas knockdown of circ1811 led to the opposite effects. AGO2 RIP and dual luciferase reporter assays indicated that circ1811 directly sponges miR-632 to upregulate the expression of DAPK1. Collectively, circ1811 acts as a tumor-suppressor for GC progression by regulating the miR-632/DAPK1 axis. Our findings suggest the potential of circ1811 as ideal biomarker and therapeutic target for GC.
引用
收藏
页数:15
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