CircRBMS3 promotes gastric cancer tumorigenesis by regulating miR‐153–SNAI1 axis. Issue 3 (21st August 2018)

• Record Type: Journal Article
• Authors: Li, Guangyan; Xue, Minghui; Yang, Fang; Jin, Yuhong; Fan, Yingying; Li, Wei
• Is Part Of: Journal of cellular physiology. Volume 234:Issue 3(2019:Mar.)
• Page Start: 3020
• Page End: 3028
• Publication Date: 2018-08-21
• Subjects: circRBMS3 -- gastric cancer -- miR‐153 -- SNAI1; Physiology -- Periodicals; Cell physiology -- Periodicals; 571.6
• DOI: 10.1002/jcp.27122
• Languages: English
• ISSNs: 0021-9541

Abstract

Abstract: Gastric cancer (GC) is one of the leading causes of cancer‐related death worldwide. Mounting evidence showed that circular RNAs (circRNAs) play critical roles in human malignancy. However, the knowledge about circRNAs in GC is still unclear. In the current study, high throughput microarray assay showed that circRBMS3 was upregulated in GC tissues, which was further confirmed by quantitative reverse transcription polymerase chain reaction. Correlation analysis revealed that high circRBMS3 expression was associated with advanced TNM stage, depth of invasion, and lymph‐node metastasis. Kaplan–Meier analysis indicated that GC patients with high circRBMS3 expression have a poor overall survival (OS). Function assays showed that circRBMS3 silencing reduced GC cells proliferation and invasion in vitro, and inhibited the tumor growth in vivo. Mechanistically, we found that miR‐153 could act as a target of circRBMS3. Subsequently, we showed that circRBMS3 promoted snail family zinc finger 1 (SNAI1) expression via inhibiting miR‐153 in GC cells. Collectively, these results suggested that circRBMS3 promoted GC cells proliferation and invasion via regulating miR‐153/SNAI1 axis. Abstract : CircRBMS3 could act as an oncogenic circRNA in GC progression. CircRBMS3 upregulation in GC elevated snail family zinc finger 1 expression via targeting miR‐153.