Retracted: CircRNA_103948 inhibits autophagy in colorectal cancer in a ceRNA manner

自噬 竞争性内源性RNA 结直肠癌 癌症研究 癌症 计算生物学 生物 肿瘤科 医学 内科学 遗传学 基因 核糖核酸 长非编码RNA 细胞凋亡
作者
Nanyang Zhang,Xianxiang Zhang,Wenjian Xu,Xiaoxiao Zhang,Zepeng Mu
出处
期刊:Annals of the New York Academy of Sciences [Wiley]
卷期号:1503 (1): 88-101 被引量:16
标识
DOI:10.1111/nyas.14679
摘要

Circular RNA (circRNA) is implicated in many types of cancer; however, the expression and role of circRNAs in colorectal cancer (CRC) remains poorly understood. In this study, a circRNA microarray assay was performed to detect abnormally expressed circRNAs in CRC, and tissue arrays were used to determine the prognosis for CRC patients. Cell counting kit-8, clone formation, wound healing, and transwell assays were used to evaluate cell functions in vitro, and a mouse subcutaneous tumor model was designed for in vivo analysis. Autophagy was observed using confocal laser scanning and transmission electron microscopy. The expression of circRNA, miRNA, and mRNA was detected using qPCR; western blot, RNA pull-down assay, RNA immunoprecipitation, and dual luciferase assessment were applied for mechanistic studies. We found that circRNA_103948 expression is upregulated in CRC tissues, compared with adjacent normal tissues, and associated with poor prognosis. Knockdown of circRNA_103948 suppressed CRC both in vitro and in vivo. Mechanistically, circRNA_103948 could directly bind to miR-1236-3p and relieve suppression of the target TPT1. Furthermore, circRNA_103948 inhibited autophagy of CRC cells. Taken together, circRNA_103948 knockdown inhibited CRC cell growth by targeting miR-1236-3p/TPT1 axis-mediated autophagy. Thus, the circRNA_103948/miR-1236-3p/TPT1 axis affects CRC progression via modulation of autophagy.
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