CircABCA13 acts as a miR-4429 sponge to facilitate esophageal squamous cell carcinoma development by stabilizing SRXN1.
Junwen LuoZhongxian TianYongjia ZhouZhaohua XiaoSun Young ParkHong SunTing ZhuangYongjie WangPeiwei LiXiaogang ZhaoPublished in: Cancer science (2023)
Circular RNAs (circRNAs) play a pivotal role in the tumorigenesis and progression of various cancers. However, the role and mechanisms of circABCA13 in esophageal squamous cell carcinoma (ESCC) are largely unknown. Here, we reported that circABCA13, a novel circular RNA generated by back-splicing of the intron of the ABCA13 gene, is highly expressed in ESCC tumor tissues and cell lines. Upregulation of circABCA13 correlated with TNM stage and a poor prognosis in ESCC patients. While knockdown of circABCA13 in ESCC cells significantly reduced cell proliferation, migration, invasion, and anchorage-independent growth, overexpression of circABCA13 facilitated tumor growth both in vitro and in vivo. In addition, circABCA13 directly binds to miR-4429 and sequesters miR-4429 from its' endogenous target, SRXN1 mRNA, which subsequently upregulates SRXN1 and promotes ESCC progression. Consistently, overexpression of miR-4429 with mimics or knockdown of SRXN1 in ESCC cells attenuated circABCA13-induced malignant behavior in vitro and in vivo. Collectively, our study uncovered the oncogenic role of circABCA13 and its mechanism in ESCC, suggesting that circABCA13 could be a potential therapeutic target and a predictive biomarker for ESCC patients.
Keyphrases
- cell proliferation
- long non coding rna
- poor prognosis
- end stage renal disease
- induced apoptosis
- cell cycle
- ejection fraction
- long noncoding rna
- newly diagnosed
- prognostic factors
- pi k akt
- chronic kidney disease
- transcription factor
- cell cycle arrest
- young adults
- risk assessment
- gene expression
- patient reported outcomes
- cell migration