Volume 26, Issue 5 pp. 432-441
Original Article

Differential expression analysis of urinary exosomal circular RNAs in patients with IgA nephropathy

Rumei Luan

Rumei Luan

Department of Nephrology, The Second Hospital of Jilin University, Changchun, China

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Geng Tian

Geng Tian

Department of Gynaecology and Obstetrics, The Second Hospital of Jilin University, Changchun, China

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Xin Ci

Xin Ci

Department of Nephrology, The Second Hospital of Jilin University, Changchun, China

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Qian Zheng

Qian Zheng

Department of Nephrology, The Second Hospital of Jilin University, Changchun, China

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Linlin Wu

Linlin Wu

Department of Nephrology, The Second Hospital of Jilin University, Changchun, China

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Xuehong Lu

Corresponding Author

Xuehong Lu

Department of Nephrology, The Second Hospital of Jilin University, Changchun, China

Correspondence

Xuehong Lu, Department of Nephrology, Second Hospital, Jilin University, 218 Ziqiang Street, Changchun, Jilin 130041, China.

Email: [email protected]

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First published: 26 January 2021
Citations: 21

Rumei Luan and Geng Tian contributed equally to this study.

Funding information: Hygiene and Health Technology Innovation Project of Jilin Province, Grant/Award Number: 2020J037; Jilin University; Health Commission of Jilin Province

Abstract

Aims

Immunoglobulin A nephropathy (IgAN) is the most common primary glomerular disease to cause end-stage kidney disease. This study investigated the difference in urinary exosomal circular RNA (circRNA) expression profiles between patients with IgAN and healthy controls (HCs), for better understanding of gene regulation in exosomes of IgAN patients.

Methods

A pairwise comparison of urinary circRNA expression profiles between IgAN patients and HCs was performed using methods, including high-throughput sequencing and quantitative polymerase chain reaction. Moreover, the potential functions of differentially expressed circRNAs (DECs) in IgAN were investigated by gene ontology (GO) enrichment analysis; Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis; and the circRNA-miRNA-mRNA network.

Results

We identified 450 upregulated and 26 downregulated circRNAs in the IgAN patients. GO analysis showed that these enriched circRNAs might regulate primary miRNA processing, the ability of angiotensin receptor binding, and stress fibre function. KEGG analysis suggested these DECs may be closely associated with the phosphoinositide-3-kinase-protein kinase B/Akt (PI3K-Akt) signalling pathways. Network analysis revealed the relationship between circRNAs and their target genes.

Conclusion

The identified DECs may be useful for both researches on molecular aetiology of IgAN and development of potentially novel non-invasive biomarkers of IgAN.

CONFLICTS OF INTEREST

All authors have read and filled out the journal's ICMJE Form. The other authors declare no potential conflicts of interest and the article has been reviewed and approved by all authors.

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