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Integrated Analysis of the CircRNA-Based ceRNA Network in Renal Fibrosis Induced by Ischemia Reperfusion Injury.
Wei, Lei; Yu, Zhixiang; Liu, Limin; Zhou, Ying; Bai, Xiao; Wang, Liya; Bai, Ming; Sun, Shiren.
Afiliación
  • Wei L; Department of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
  • Yu Z; State Key Laboratory of Cancer Biology, Fourth Military Medical University, Xi'an, China.
  • Liu L; Department of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
  • Zhou Y; State Key Laboratory of Cancer Biology, Fourth Military Medical University, Xi'an, China.
  • Bai X; Department of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
  • Wang L; Department of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
  • Bai M; State Key Laboratory of Cancer Biology, Fourth Military Medical University, Xi'an, China.
  • Sun S; Department of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Front Genet ; 12: 793182, 2021.
Article en En | MEDLINE | ID: mdl-35222519
Background: Circular RNAs (circRNAs), which have broad posttranscriptional regulatory potencies, are involved in the pathogenesis of fibrotic diseases and are promising diagnostic biomarkers and therapeutic targets. However, their specific roles in renal fibrosis remain elusive. Methods: A robust unilateral renal ischemia reperfusion injury (UIRI) mouse model was established to recapitulate the pathophysiology of renal fibrosis. The expression of circRNAs, miRNAs, and mRNAs was profiled by high-throughput RNA sequencing technology. Results: In total, 4983 circRNAs, 216 miRNAs, and 6371 mRNAs were differentially expressed in UIRI-induced fibrotic kidneys. Candidate circRNAs and miRNAs were validated by RT-qPCR in both UIRI and unilateral ureteral obstruction mouse models. Bioinformatic analysis indicated that the parental genes of the differentially expressed circRNAs were predominantly implicated in focal adhesion, adhesion junctions, and regulation of actin cytoskeleton pathways. Through circRNA-miRNA-mRNA construction, we identified two hub genes, circSlc8a1 and circApoe, that targeted a large number of differentially expressed miRNAs and mRNAs related to metabolism and cytokine-cytokine receptor pathways, respectively. Conclusion: CircRNAs were dysregulated in the UIRI model and might be potentially involved in the pathogenesis of renal fibrosis. Research efforts should focus on unravelling the functions of aberrantly expressed circRNAs in renal fibrosis to uncover biomarkers that would enable early diagnosis and the design of prompt therapeutic interventions to prevent disease progression.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Screening_studies Idioma: En Revista: Front Genet Año: 2021 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Screening_studies Idioma: En Revista: Front Genet Año: 2021 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza