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Published on: April 25, 2017
CircRNA/miRNA/mRNA axis participates in the progression of partial bladder outlet obstruction
Baoyi Zhu1, Jun Gao2, Yuying Zhang3
1Department of Urology, The Sixth Affiliated Hospital of Guangzhou Medical University (Qingyuan People's Hospital), B24 Yinquan Road, Qingcheng, Qingyuan, 511500, Guangdong, People's Republic of China.
Background:
More and more evidence showed that circRNA/miRNA/mRNA axis played a vital role in the pathogenesis of some diseases. However, the role of circRNA/miRNA/mRNA axis in partial bladder outlet obstruction (pBOO) remains unknown. Our study aimed to explore the complex regulatory mechanism of circRNA/miRNA/mRNA axis in pBOO.
Methods:
The pBOO rat model was established, and the bladder tissues were collected for mRNA sequencing. The differentially expressed mRNAs were analyzed by high-throughput sequencing, and the GO and KEGG analysis of the differentially expressed mRNAs were performed. Competing endogenous RNAs (ceRNAs) analysis identified the potential regulation function of circRNA/miRNA/mRNA axis in pBOO. qRT-PCR detected the expression of circRNA/miRNA/mRNA. miRanda software was performed to predict the relationship between circRNA and miRNA, miRNA and mRNA.
Results:
Compared with the sham group, a total of 571 mRNAs were differentially expressed in the pBOO group, of which 286 were up-regulated and 285 were down-regulated. GO analysis showed that the mRNAs were mainly involved in cellular process, single-organism process, and cell, etc. KEGG analysis showed that the enriched signaling pathways were metabolic pathways, cell adhesion molecules (CAMs), and HTLV-I infection, etc. Based on the previous transcriptome data and differentially expressed circRNAs, we drew the ceRNA network regulation diagram. qRT-PCR results confirmed that chr3:113195876|113197193/rno-miR-30c-1-3p/Gata4, chr1:126188351|126195625/rno-miR-153-5p/Diaph3, and chr9:81258380|81275269/rno-miR-135b-5p/Pigr axis may have ceRNA function. miRanda confirmed there have the binding sites of circRNA/miRNA/mRNA axis.
Conclusions:
CircRNA/miRNA/mRNA axis was involved in the progression of pBOO. Our research on the circRNA/miRNA/mRNA axis revealed new pathogenesis and treatment strategies for pBOO.
Insights
The circRNA/miRNA/mRNA axis is implicated in the progression of partial bladder outlet obstruction (pBOO). This study identified key regulatory pathways, offering potential new therapeutic strategies for pBOO.
Area of Science:
- Molecular Biology
- Genetics
- Urology
Background:
- Circular RNAs (circRNAs), microRNAs (miRNAs), and messenger RNAs (mRNAs) form regulatory axes crucial in disease pathogenesis.
- The specific role of the circRNA/miRNA/mRNA axis in partial bladder outlet obstruction (pBOO) remains largely unexplored.
- Understanding these interactions is vital for elucidating disease mechanisms.
Purpose of the Study:
- To investigate the complex regulatory mechanisms of the circRNA/miRNA/mRNA axis in the context of pBOO.
- To identify key molecular players and pathways involved in pBOO pathogenesis.
- To explore potential therapeutic targets for pBOO.
Main Methods:
- Establishment of a pBOO rat model and collection of bladder tissues.
- High-throughput mRNA sequencing to identify differentially expressed mRNAs.
- Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses.
- Competing endogenous RNA (ceRNA) network analysis to predict circRNA/miRNA/mRNA interactions.
- Quantitative real-time PCR (qRT-PCR) for expression validation.
- miRanda software for predicting binding sites between RNA molecules.
Main Results:
- A total of 571 differentially expressed mRNAs were identified in the pBOO group compared to the sham group (286 up-regulated, 285 down-regulated).
- GO analysis indicated involvement in cellular processes, single-organism processes, and cellular functions.
- KEGG analysis highlighted enriched pathways including metabolic pathways, cell adhesion molecules (CAMs), and HTLV-I infection.
- ceRNA network analysis and qRT-PCR validation suggested potential roles for specific circRNA/miRNA/mRNA axes (e.g., chr3:113195876|113197193/rno-miR-30c-1-3p/Gata4).
Conclusions:
- The circRNA/miRNA/mRNA axis plays a significant role in the progression of pBOO.
- This research provides novel insights into the pathogenesis of pBOO.
- The identified regulatory axes may represent promising targets for future pBOO treatment strategies.
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