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MicroRNA expression profile in chronic nonbacterial prostatitis revealed by next-generation small RNA sequencing


1 Department of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei 230022, China
2 Institute of Urology, Anhui Medical University, Hefei 230022, China
3 Anhui Province Key Laboratory of Genitourinary Diseases, Anhui Medical University, Hefei 230022, China

Correspondence Address:
Chao-Zhao Liang,
Department of Urology, The First Affiliated Hospital of Anhui Medical University; Institute of Urology; Anhui Province Key Laboratory of Genitourinary Diseases, Anhui Medical University, Hefei 230022
China
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/aja.aja_97_18

PMID: 30604696

MicroRNAs (miRNAs) are considered to be involved in the pathogenic initiation and progression of chronic nonbacterial prostatitis (CNP); however, the comprehensive expression profile of dysregulated miRNAs, relevant signaling pathways, and core machineries in CNP have not been fully elucidated. In the current research, CNP rat models were established through the intraprostatic injection of carrageenan into the prostate. Then, next-generation sequencing was performed to explore the miRNA expression profile in CNP. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) bioinformatical analyses were conducted to reveal the enriched biological processes, molecular functions, and cellular components and signaling pathways. As a result, 1224, 1039, and 1029 known miRNAs were annotated in prostate tissues from the blank control (BC), normal saline injection (NS), and carrageenan injection (CAR) groups (n = 3 for each group), respectively. Among them, 84 miRNAs (CAR vs BC) and 70 miRNAs (CAR vs NS) with significantly different expression levels were identified. Compared with previously reported miRNAs with altered expression in various inflammatory diseases, the majority of deregulated miRNAs in CNP, such as miR-146b-5p, miR-155-5p, miR-150-5p, and miR-139-5p, showed similar expression patterns. Moreover, bioinformatics analyses have enriched mitogen-activated protein kinase (MAPK), cyclic adenosine monophosphate (cAMP), endocytosis, mammalian target of rapamycin (mTOR), and forkhead box O (FoxO) signaling pathways. These pathways were all involved in immune response, which indicates the critical regulatory role of the immune system in CNP initiation and progression. Our investigation has presented a global view of the differentially expressed miRNAs and potential regulatory networks containing their target genes, which may be helpful for identifying the novel mechanisms of miRNAs in immune regulation and effective target-specific theragnosis for CNP.


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