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Series GSE218574 Query DataSets for GSE218574
Status Public on Jun 28, 2023
Title The angiogenic role of circRNA-007371 in liver fibrosis [circRNA Microarray]
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary Objective Circular RNAs (circRNAs) are covalently closed, endogenous non-coding RNAs. CircRNAs play a vital role in liver diseases, acting as microRNA (miRNA) sponges. However, the angiogenic role of circRNA remains unknown in liver fibrosis and is the focus of this study. Methods Liver fibrosis was induced by thioacetamide (TAA), or carbon tetrachloride (CCl4) in mice. CircRNA-microarray, AGO2-RNA immunoprecipitation (RIP), and RNA-seq were utilized to explore the hepatic circRNAs profile. The qPCR and PCR-gel electrophoresis analysis were used to investigate the characterization of circRNA-007371. Liver tissues and EMOA murine endothelial cells were used to verify the angiogenic mechanism of circRNA-007371. Results The increased collagen deposition, pseudolobule formation, and angiogenesis were observed in murine liver induced by TAA and CCl4. CircRNA-microarray in TAA-induced fibrotic murine liver indicated that the expression of circRNA-007371 was up-regulated. Moreover, AGO2-RIP and PCR analysis showed that circRNA-007371 had the characterization of circRNAs and played a role as competing endogenous RNAs (ceRNA) sponging miR-200a. In vitro, circRNA-007371 promoted the ability of migration, growth, and blood vessel formation in EMOA murine endothelial cells using wound healing and tube formation assay. The AGO2-RIP and RNA-sequencing analysis in overexpression circRNA-007371 EMOA murine endothelial cells demonstrated that circRNA-007371 upregulates the stromal antigen 1 (Stag1) via spouse of miR-200a and HIF-1 signaling pathway might participate in the angiogenesis. Conclusions This study discovers that circRNA-007371, a novel ceRNA, is up-regulated, and enhances the angiogenesis via angiocrine role to regulate the STAG1-miR-200a-5p signaling pathway in liver fibrosis.
 
Overall design 1. One liver fibrosis model was induced by intraperitoneal injection of thioacetamide (TAA) in C57BL/6J mice for 8 weeks. Control mice received the same volume of normal saline (NS). Another model was induced by intraperitoneal injection of carbon tetrachloride (CCl4) in C57BL/6J mice for 6 weeks. Control mice received the same volume of olive oil. 2. The mouse hemangioendothelioma endothelial cells (EOMA) were transfected with circRNA-007371 overexpression plasmid.
 
Contributor(s) Zhao C, Qian S, Tai Y, Tang C, Huang Z, Gao J
Citation(s) 36854930
Submission date Nov 22, 2022
Last update date Jun 29, 2023
Contact name shuaijie qian
E-mail(s) qsjbxh1997@outlook.com
Phone 13540675514
Organization name West China Hospital, Sichuan University
Lab Lab of Gastroenterology and Hepatology
Street address NO. 1, 4th Keyuan Road, Chengdu,
City chengdu
State/province sichuan
ZIP/Postal code 610041
Country China
 
Platforms (1)
GPL32873 Arraystar Mouse circRNA Array
Samples (10)
GSM6752753 Liver_saline_8W_rep1
GSM6752754 Liver_saline_8W_rep2
GSM6752755 Liver_saline_8W_rep3
This SubSeries is part of SuperSeries:
GSE218581 The angiogenic role of circRNA-007371 in liver fibrosis
Relations
BioProject PRJNA904333

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE218574_CircRNA_Expression_Profiling_Data.xls.gz 425.0 Kb (ftp)(http) XLS
GSE218574_Differentially_Expressed_CircRNAs.xls.gz 57.0 Kb (ftp)(http) XLS
GSE218574_RAW.tar 5.4 Mb (http)(custom) TAR (of GPR)
Processed data included within Sample table
Processed data are available on Series record

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