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Circ_0136474 and MMP-13 suppressed cell proliferation by competitive binding to miR-127-5p in osteoarthritis
Zhao Li1,2, Bo Yuan3, Zheng Pei2
1Center of Arthritis Clinic & Research, Peking University People's Hospital, Beijing, China.
Abstract:
Osteoarthritis (OA) is a prevalent degenerative joint disease whose pathogenesis remains unclear. The research aims to investigate the roles of Circ_0136474/miR-127-5p/MMP-13 axis in OA. Differentially expressed circRNAs and miRNAs in OA cartilage tissue were screened out and visualized by R project based on RNA-seq data and microarray data respectively. qRT-PCR was carried out for detection of relative expression levels of Circ_0136474, miR-127-5p, MMP-13 and other inflammatory factors and Western blot analysis was conducted to detect the protein expression level of MMP-13. CCK-8 assay and flow cytometry were conducted to determine cell proliferation and cell apoptotic ability respectively. RNA-fluorescence in situ hybridization (RNA-FISH) experiments were conducted to confirm the immune-localization of the Circ_0136474 and MMP-13 in human tissues. Targeted relationships were predicted by bioinformatic analysis and verified by dual-luciferase reporter assay. Our findings revealed that the expression levels of both Circ_0136474 and MMP-13 in OA cartilage tissue were significantly higher than that in normal cartilage tissue. Circ_0136474 could suppress cell proliferation by facilitating MMP-13 expression and suppressing miR-127-5p expression in OA. Overexpression of miR-127-5p negatively regulated MMP-13 expression to enhance cell proliferation. Our study demonstrated that Circ_0136474 and MMP-13 suppressed cell proliferation, while enhanced cell apoptosis by competitive binding to miR-127-5p in OA, which may well provide us with a new therapeutic strategy for osteoarthritis.
Insights
This study reveals that Circ_0136474 and MMP-13 suppress cell proliferation and enhance apoptosis in osteoarthritis (OA) by interacting with miR-127-5p. These findings suggest a new therapeutic strategy for OA.
Area of Science:
- Molecular Biology
- Genetics
- Biochemistry
Background:
- Osteoarthritis (OA) is a common degenerative joint disease with incompletely understood mechanisms.
- Identifying key molecular players in OA pathogenesis is crucial for developing effective treatments.
Purpose of the Study:
- To investigate the role of the Circ_0136474/miR-127-5p/MMP-13 axis in the development of osteoarthritis.
- To explore potential therapeutic targets for OA based on this molecular axis.
Main Methods:
- RNA sequencing and microarray analysis to identify differentially expressed circRNAs and miRNAs in OA cartilage.
- Quantitative real-time PCR (qRT-PCR) and Western blot to assess gene and protein expression levels.
- Cell proliferation (CCK-8 assay) and apoptosis (flow cytometry) assays.
- Bioinformatic analysis and dual-luciferase reporter assays to confirm molecular interactions.
Main Results:
- Circ_0136474 and MMP-13 expression were significantly elevated in OA cartilage compared to normal cartilage.
- Circ_0136474 promotes MMP-13 expression and inhibits miR-127-5p, suppressing cell proliferation in OA.
- Overexpression of miR-127-5p inhibits MMP-13 and enhances cell proliferation.
- The Circ_0136474/miR-127-5p/MMP-13 axis influences cell proliferation and apoptosis in OA.
Conclusions:
- The Circ_0136474/miR-127-5p/MMP-13 axis plays a significant role in osteoarthritis pathogenesis.
- Circ_0136474 and MMP-13 negatively regulate cell proliferation and promote apoptosis in OA via miR-127-5p.
- This axis represents a potential novel therapeutic target for osteoarthritis treatment.
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