期刊论文详细信息
Molecular Cancer
circCHST15 is a novel prognostic biomarker that promotes clear cell renal cell carcinoma cell proliferation and metastasis through the miR-125a-5p/EIF4EBP1 axis
Bing Liao1  Jia-Zheng Cao2  Yi Hou3  Hai-Shan Lin3  Hao-Hua Yao3  Hong-De Song3  Cheng-Gong Luo3  Gao-Sheng Yao3  Quan-Hui Xu3  Yu-Hang Chen3  Yi-Ming Tang3  Jin-Huan Wei3  Jia-Ying Li3  Cheng-Peng Gui4  Jun-Hang Luo4  Lei Tan5 
[1] Department of Pathology, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China;Department of Urology, Affiliated Jiangmen Hospital, Sun Yat-sen University, 529000, Jiangmen, Guangdong, China;Department of Urology, First Affiliated Hospital, Sun Yat-sen University, 510080, Guangzhou, Guangdong, China;Department of Urology, First Affiliated Hospital, Sun Yat-sen University, 510080, Guangzhou, Guangdong, China;Institute of Precision Medicine, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China;Department of Urology, Nanfang Hospital, Southern Medical University, 510515, Guangzhou, Guangdong, China;
关键词: hsa_circ_0020303;    miR-125a-5p;    EIF4EBP1;    Proliferation;    Metastasis;    Clear cell renal cell carcinoma;   
DOI  :  10.1186/s12943-021-01449-w
来源: Springer
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【 摘 要 】

BackgroundCircular RNAs (circRNAs) have been indicated as potentially critical mediators in various types of tumor progression, generally acting as microRNA (miRNA) sponges to regulate downstream gene expression. However, the aberrant expression profile and dysfunction of circRNAs in human clear cell renal cell carcinoma (ccRCC) need to be further investigated. This study mined key prognostic circRNAs and elucidates the potential role and molecular mechanism of circRNAs in regulating the proliferation and metastasis of ccRCC.MethodscircCHST15 (hsa_circ_0020303) was identified by mining two circRNA microarrays from the Gene Expression Omnibus database and comparing matched tumor versus adjacent normal epithelial tissue pairs or matched primary versus metastatic tumor tissue pairs. These results were validated by quantitative real-time polymerase chain reaction and agarose gel electrophoresis. We demonstrated the biological effect of circCHST15 in ccRCC both in vitro and in vivo. To test the interaction between circCHST15 and miRNAs, we conducted a number of experiments, including RNA pull down assay, dual-luciferase reporter assay and fluorescence in situ hybridization.ResultsThe expression of circCHST15 was higher in ccRCC tissues compared to healthy adjacent kidney tissue and higher in RCC cell lines compared to normal kidney cell lines. The level of circCHST15 was positively correlated with aggressive clinicopathological characteristics, and circCHST15 served as an independent prognostic indicator for overall survival and progression-free survival in patients with ccRCC after surgical resection. Our in vivo and in vitro data indicate that circCHST15 promotes the proliferation, migration, and invasion of ccRCC cells. Mechanistically, we found that circCHST15 directly interacts with miR-125a-5p and acts as a microRNA sponge to regulate EIF4EBP1 expression.ConclusionsWe found that sponging of miR-125a-5p to promote EIF4EBP1 expression is the underlying mechanism of hsa_circ_0020303-induced ccRCC progression. This prompts further investigation of circCHST15 as a potential prognostic biomarker and therapeutic target for ccRCC.

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